The Role of Macrophages in Acute and Chronic Wound Healing and Interventions to Promote Pro-wound Healing Phenotypes — TEI-tagged view

Paulina KrzyszczykpersName, Rene SchlosspersName, Andre F. PalmerpersName, François BerthiaumepersName (2018date). “The Role of Macrophages in Acute and Chronic Wound Healing and Interventions to Promote Pro-wound Healing Phenotypes.” Frontiers in Physiologytitle·j.

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Abstract. Macrophagesterm·dom play key roles in all phases of adult wound healingterm·dom, which are inflammationterm·dom, proliferation, and remodeling. As wounds heal, the local macrophageterm·dom population transitions from predominantly pro-inflammatory (M1-like phenotypes) to anti-inflammatory (M2-like phenotypes). Non-healing chronic woundsterm·dom, such as pressure, arterial, venous, and diabetic ulcers indefinitely remain in inflammationterm·dom—the first stage of wound healingterm·dom. Thus, local macrophagesterm·dom retain pro-inflammatory characteristics. This reviewterm·mth discusses the physiology of monocytes and macrophagesterm·dom in acute wound healingterm·dom and the different phenotypes described in the literature for both in vitro and in vivo models. We also discuss aberrations that occur in macrophageterm·dom populations in chronic woundsterm·dom, and attempts to restore macrophageterm·dom function by therapeutic approaches. These include endogenous M1 attenuation, exogenous M2 supplementation and endogenous macrophageterm·dom modulation/M2 promotion via mesenchymal stem cells, growth factors, biomaterials, heme oxygenase-1 (HO-1) expression, and oxygen therapy. We recognize the challenges and controversies that exist in this field, such as standardization of macrophageterm·dom phenotype nomenclature, definition of their distinct roles and understanding which phenotype is optimal in order to promote healing in chronic woundsterm·dom. Clinical and economic significance of chronic woundsterm·dom Following surgical incisions and minor lacerations, diabetic, venous, and pressure ulcers are the most common wounds on a global scale (MedMarket Diligence, 2012 , 2015 ). Whereas, a majority of surgical incisions and lacerations are categorized as acute wounds and often heal with minimal complications, ulcers are chronic woundsterm·dom that resist healing and require expensive treatments. Furthermore, as surgical wounds become less of a problem due to the advances of minimally invasive surgery, chronic woundsterm·dom are on the rise, as they often occur in growing populations, such as the elderly, obese, and diabetic. In recent years, there were ~4.5, 9.7, and 10 million pressure, venous, and diabetic ulcer wound patients globally (MedMarket Diligence, 2012 , 2015 ). The numbers of pressure and venous ulcers are rising at rates of 6–7% annually, and growth is even larger for diabetic ulcers (9%) due to the increased incidence of diabetes in the developed world. Unfortunately, the staggering number of chronic, non-healing wounds is growing much faster than the emergence of new, effective therapies. Standard wound care involves patient and wound assessments, offloading, debridement of necrotic and infected tissue, treatment with antibiotics, and regular wound dressing changes (Falanga, 2005 ; Frykberg and Banks, 2015 ). Advanced therapies are available for wounds that do not improve after several weeks of standard care. These include negative pressure wound therapy, topically applied platelet-derived growth factor (PDGF) (Regranex), acellular extracellular matrices (Integra, Matristem, Theraskin), and bioengineered cell-containing therapies (Apligraf, Dermagraft), to name a few. Other possible treatments include hyperbaric or topical oxygen treatment in order to restore oxygen to the wound. In the case of wounds in which infection and severe tissue damage cannot be controlled, the effects of which may otherwise be life-threatening, amputation is performed. In fact, two thirds of all lower-limb amputations are due to diabetic ulcers (Sen et al., 2009 ). Since many chronic woundsterm·dom do not improve with standard care, treatment quickly becomes expensive with the introduction of advanced therapies, and sometimes amputation. With so many people suffering from chronic woundsterm·dom, and so many failed attempts at treating them, it is not surprising that wound care costs are also enormous. In the United States, over $25 billion dollars are spent annually on chronic woundterm·dom care (Sen et al., 2009 ). In England, costs for pressure ulcer treatment can reach up to 6500 pounds per patient (>$8,000 U.S. dollars) (Posnett and Franks, 2008 ). Similarly, in the United States, the average cost of Medicare spending on pressure and arterial ulcers in 2014 was $3696 and $9015 per patient, respectively—the two most expensive of all types of wounds included in the study (Nussbaum et al., 2018 ). Furthermore, each amputation procedure can cost well over $35,000 (Gordois et al., 2003 ; Sen et al., 2009 ; Carls et al., 2011 ). Due to the increasing prevalence of diabetes in the U.S., the total cost of diabetic ulcer care has also drastically increased in the past 20 years (Nussbaum et al., 2018 ). There is an urgent need to understand the pathophysiology of non-healing wounds in order to develop effective therapies that restore their ability to resolve and heal. The wound healingterm·dom process and chronic vs. acute wounds Chronic woundsterm·dom fail to heal, despite the use of current therapies, because they are stalled in the early inflammatory state within the wound healingterm·dom stages (Zhao et al., 2016 ). In contrast, acute wounds progress through this process in a timely manner as they heal. The wound healingterm·dom process is composed of three overlapping phases: inflammationterm·dom, proliferation and remodeling (Singer and Clark, 1999 ; Baum and Arpey, 2005 ; Liu and Velazquez, 2008 ). After skin injury occurs, platelets are activated at the site of blood vessel rupture and promote clot formation to stop blood loss. Platelets also release factors that attract immune cells from the circulation into the wound. This marks the beginning of the inflammatory phase. Polymorphonuclear neutrophils are first to arrive, followed by monocytes that quickly differentiate into macrophagesterm·dom (Sindrilaru and Scharffetter-Kochanek, 2013 ). Neutrophils produce high levels of reactive oxygen species (ROS), proteases and pro-inflammatory cytokines to sanitize the wound. When this process is complete, neutrophils apoptose and become phagocytosed by the newly arrived macrophagesterm·dom. Macrophagesterm·dom will also phagocytose bacteria and debris in order to clean the wound (Frykberg and Banks, 2015 ). During this time, the wound is sterilized and prepared for tissue regrowth, which occurs in the proliferative phase (Baum and Arpey, 2005 ). As the name indicates, wound cells proliferate and migrate during this phase, in order to regenerate the lost tissue. This includes endothelial cells, fibroblasts and keratinocytes. A preliminary, vascularized extracellular matrix (ECM), called the granulation tissue (GT), is laid down and keratinocytes migrate upon it to close the wound. During remodeling, the final phase of wound healingterm·dom, ECM within the granulation tissue matures and increases in mechanical strength (Falanga, 2005 ). Wound healingterm·dom is complete following apoptosis of myofibroblasts and vascular cells, leaving behind a collagen-rich scar (Zhao et al., 2016 ). In chronic woundsterm·dom, the proliferative and remodeling stages do not readily occur (Zhao et al., 2016 ). The wound remains in the inflammatory phase, which does not favor tissue regeneration, and therefore, the wound cannot heal (Frykberg and Banks, 2015 ). Targeting and correcting cellular and molecular causes of prolonged inflammationterm·dom in chronic woundsterm·dom may be an effective method to return them to healing states. The general role of macrophagesterm·dom in wound healingterm·dom There is considerable evidence that macrophagesterm·dom are key regulators of the wound healingterm·dom process, during which they take on distinct roles to ensure proper healing. It is well-established that the phenotype of macrophagesterm·dom evolves with the stages of wound healingterm·dom (Mosser and Edwards, 2008 ; Ferrante and Leibovich, 2012 ). Initially, pro-inflammatory macrophagesterm·dom, traditionally referred to as “M1” macrophagesterm·dom, infiltrate after injury in order to clean the wound of bacteria, foreign debris and dead cells. In acute wounds, as the tissue begins to repair, the overall macrophageterm·dom population transitions to one that promotes anti-inflammatory effects (traditionally and collectively referred to as “M2” macrophagesterm·dom), and the migration and proliferation of fibroblasts, keratinocytes and endothelial cells to restore the dermis, epidermis and vasculature, respectively. This process will eventually close the wound and produce a scar. Macrophagesterm·dom also play particularly important roles in vascularization, by positioning themselves nearby newly forming blood vessels and aiding in their stabilization and fusion (Fantin et al., 2010 ; Ogle et al., 2016 ). In the beginning of the final remodeling phase, macrophagesterm·dom release matrix metalloproteinases (MMPs) to breakdown the provisional extracellular matrix, and then apoptose so that the skin can mature to its original, non-wounded state (Vannella and Wynn, 2017 ). In chronic woundsterm·dom, pro-inflammatory macrophagesterm·dom persist without transitioning to anti-inflammatory phenotypes, which is believed to contribute to the impairment in tissue repair (Zhao et al., 2016 ; Hesketh et al., 2017 ). Macrophageterm·dom phenotype readily changes based on spatiotemporal cues during wound healingterm·dom, and several different subsets of macrophagesterm·dom, beyond the limited confines of simply M1 and M2 (Martinez and Gordon, 2014 ), have been defined depending on their cell surface markers, cytokine/growth factor/chemokine production, and function (detailed in section Macrophageterm·dom Phenotypes). The goal of this reviewterm·mth is to highlight the importance of macrophagesterm·dom as they pertain to acute and chronic woundterm·dom healing. The physiology of monocyte recruitment, macrophageterm·dom differentiation, and their roles in wound healingterm·dom are also discussed. Evidence toward a stalled pro-inflammatory macrophageterm·dom phenotype in chronic woundsterm·dom is also presented. Lastly, examples are provided of several different approaches that have been taken toward attenuating pro-inflammatory (M1-like) macrophagesterm·dom and promoting anti-inflammatory (M2-like) macrophagesterm·dom in order to heal chronic woundsterm·dom. It is important to note that, due to the complexity of macrophagesterm·dom, there are several unanswered questions and controversial topics within the field. These are discussed throughout the text, and are also summarized in Table 1 . Table 1 Guide to discussed macrophageterm·dom questions/controversies. Guide to Discussed Macrophageterm·dom Questions/Controversies Topic Questions/Controversy in Literature Related section Dermal Macrophagesterm·dom • What is the contribution of tissue-resident, dermal macrophagesterm·dom to wound healingterm·dom? Sections Dermal Macrophagesterm·dom and Skin Appendages, Dermal Macrophagesterm·dom and Wound Healingterm·dom Monocyte Recruitment/ Macrophageterm·dom Differentiation • Are monocytes pre-programmed to becoming a specific macrophageterm·dom phenotype prior to entering the wound and accordingly recruited when needed? • Or, does the wound microenvironment dictate monocyte differentiation/macrophageterm·dom fate? Section Monocyte Recruitment and Differentiation in Wound Healingterm·dom; Figure 1 In Vitro vs. In Vivo Macrophagesterm·dom • Do the phenotypes that are defined based on in vitro studies translate into in vivo wound macrophagesterm·dom? Section Macrophageterm·dom phenotypes M1/M2 Macrophagesterm·dom • Do macrophagesterm·dom possess distinct phenotypes with unique functions or do their characteristics form a spectrum? • Can all macrophagesterm·dom transition from one phenotype to another? • Can wound macrophagesterm·dom proliferate in situ or are they replenished by newly-infiltrated monocytes? Section Macrophageterm·dom Phenotypes; Figure 2 ; Table 2 Human vs. Murine Models • How translatable are results obtained from murine models to human chronic woundsterm·dom? Section Human vs. Murine Models Macrophagesterm·dom and Wound Healingterm·dom • Which macrophageterm·dom phenotypes/characteristics are required, and at what time, to result in effective wound healingterm·dom? Sections Macrophageterm·dom Phenotypes During Acute Wound Healingterm·dom and Macrophageterm·dom Dysregulation and Chronic Woundsterm·dom; Figure 2 Targeting Macrophagesterm·dom to Promote Wound Healingterm·dom • Are M2-like macrophagesterm·dom the answer to promoting wound healingterm·dom in all situations? If so, which specific phenotypes/characteristics? • What is the ideal treatment time for chronic woundsterm·dom in order to promote desired wound macrophagesterm·dom and wound healingterm·dom? Section Experimental Therapies and Wound Macrophagesterm·dom; Table 3 Origins of skin macrophagesterm·dom Skin macrophagesterm·dom are derived from two different sources: (1) a resident macrophageterm·dom population established before birth and (2) circulating monocytes that are recruited to areas of injury and differentiate into macrophagesterm·dom (Malissen et al., 2014 ; Vannella and Wynn, 2017 ). The first type consists of a self-renewing pool of cells derived from the embryonic yolk sack. These cells, called dermal macrophagesterm·dom, are permanent residents in healthy adult skin, often found in nearby skin appendages. In contrast, during injury, bone marrow-derived monocytes are recruited to the skin, locally differentiate into macrophagesterm·dom and play key roles in wound healingterm·dom, as discussed previously (Malissen et al., 2014 ; Vannella and Wynn, 2017 ). Dermal macrophagesterm·dom and skin appendages There are several types of well-studied tissue-resident macrophagesterm·dom throughout the body, which play important roles in their respective organs. A few examples are microglia in the brain, Kupffer cells in the liver, and alveolar macrophagesterm·dom in the lungs (Davies et al., 2013 ). Their general roles include debris clearance (e.g., surfactant in alveolar macrophagesterm·dom and red blood cells in Kupffer cells), initiation of the inflammatory response and the return to homeostasis. Due to these general functions of tissue-resident macrophagesterm·dom, it is not surprising that tissue-resident macrophagesterm·dom in skin (dermal macrophagesterm·dom) contribute to the maintenance and renewal of skin appendages during homeostasis, and wound healingterm·dom. Dermal macrophagesterm·dom are located in close proximity to hair follicles, in the surrounding connective tissue sheath and help regulate the hair growth cycle (Eichmuller et al., 1998 ; Christoph et al., 2000 ; Castellana et al., 2014 ). One of the activities of macrophagesterm·dom during hair growth is phagocytosis of collagen, to allow for matrix remodeling (Parakkal, 1969 ). In a murine model, Castellana et al. ( 2014 ) found that apoptosis of skin-resident macrophagesterm·dom activated epithelial hair follicle stem cells, which contribute to hair regeneration (Castellana et al., 2014 ). Macrophage-specific Wnt-signaling was shown to be central to this process; when it was inhibited, hair follicle growth was delayed. Apoptosis of macrophagesterm·dom occurred immediately prior to hair follicles' transition from telogen to anagen—the hair cycle's resting and growth phases, respectively. Although the study did not use a wound healingterm·dom model, the results have potential implications in regenerating hair in healing skin. In contrast, Osaka et al. 2007 used a wound model (full-thickness murine wounds) to study signaling pathways and macrophageterm·dom activation during subsequent hair growth (Osaka et al., 2007 ). They found that apoptosis signal-regulating kinase 1 (ASK1) is important for efficient hair regrowth; ASK1-deficient mice exhibited delayed hair regeneration following wounding. ASK1 has previously been shown to be increased in the epithelial layer of wound peripheries in rats (Funato et al., 1998 ). ASK1-deficient mice also had dysregulated macrophageterm·dom function; less macrophagesterm·dom were recruited to the wound site and several chemotactic and activating factors (IL-1β, TNF-α) were downregulated (Osaka et al., 2007 ). When bone-marrow derived, cytokine-stimulated macrophagesterm·dom were introduced to the wounds via intracutaneous injection in both ASK1+ and ASK1- mice, hair growth was stimulated. These studies highlight the importance of dermal macrophagesterm·dom in hair growth, which can have many implications in the development of future therapies that promote wound healingterm·dom along with hair regeneration. Although there is more research linking macrophagesterm·dom to hair follicles rather than sweat or sebaceous glands, there is still evidence that macrophagesterm·dom can also respond to cues in the microenvironment created by these appendages. For example, the type of lipids produced by sebocytes can impact whether local macrophagesterm·dom take on pro- or anti-inflammatory characteristics, which could potentially impede or promote healing in that area (Lovaszi et al., 2017 ). Overall, appendage regeneration remains one of the biggest challenges in wound repair (Takeo et al., 2015 ). Large wounds that are able to heal have a lack of hair and are unable to produce sweat and oil, which leads to cosmetic deficiencies and discomfort to patients. In general, the relationship between macrophagesterm·dom and skin appendages warrants attention, specifically in the context of wound healingterm·dom. Dermal macrophagesterm·dom and wound healingterm·dom A proposed role for tissue-resident macrophagesterm·dom during injury is that they serve as early indicators of injury or invading pathogens. Some of these macrophagesterm·dom express CD4 and are located near capillaries (Malissen et al., 2014 ). They are first-responders to injury by recognizing damage-associated molecular patterns (DAMPs; e.g., free heme, ATP) and releasing hydrogen peroxide, which initiates a powerful pro-inflammatory cascade (Minutti et al., 2017 ). In the case of infection, tissue-resident macrophagesterm·dom recognize pathogen-associated molecular patterns (PAMPs; e.g., lipopolysachharide, LPS). Responses to DAMPs and PAMPs result in the recruitment of neutrophils to help fight early infection (Malissen et al., 2014 ; Minutti et al., 2017 ). Monocyte-derived macrophagesterm·dom are also recruited to the wounded area to further amplify the inflammatory response (Davies et al., 2013 ). Although tissue-resident macrophagesterm·dom aid in the recruitment of immune cells, they are not the only cells in the wound (e.g., platelets) that produce chemokines and signals that have this effect. In general, dermal macrophagesterm·dom can be identified by several surface markers, such as CD64+, MERTK+, and CCR2-/low. They are also highly phagocytic and have a slow turnover (Malissen et al., 2014 ). Near the end of wound healingterm·dom, during resolution, dermal macrophagesterm·dom self-renew, and clear apoptotic cells as the tissue returns to homeostasis (Davies et al., 2013 ). In addition to macrophagesterm·dom, there are also dendritic cells in the skin that are derived from monocytes (e.g., Langerhans cells). These cells share many surface markers with macrophagesterm·dom, including MHCII, F4/80, CD14, and IL-10, which can make it difficult to distinguish them from each other (Malissen et al., 2014 ; Minutti et al., 2017 ). Some even consider Langerhans cells as a type of tissue-resident macrophageterm·dom, as they have a similar gene expression profile (Satpathy et al., 2012 ; Davies et al., 2013 ; Doebel et al., 2017 ; Minutti et al., 2017 ), and interestingly, a correlation between healing diabetic foot ulcers and increased numbers of Langerhans cells has been reported (Stojadinovic et al., 2013 ; Doebel et al., 2017 ). The specific role of Langerhans cells in wound healingterm·dom—particularly chronic—has yet to be defined, however, they do repopulate the epidermis during re-epithelialization in acute wound models (Stojadinovic et al., 2013 ). Monocyte recruitment and differentiation in wound healingterm·dom Whereas dermal macrophagesterm·dom initiate the local inflammatory response and have relatively short-term effects, monocyte-derived macrophagesterm·dom are systemically recruited ~24 h post-wounding (in mice) in order to heighten the inflammatory response and protect the tissue from further damage (Italiani and Boraschi, 2014 ; Minutti et al., 2017 ). Monocyte-derived macrophagesterm·dom are initially recruited to the wound by signals from damaged tissue via DAMPs or PAMPs (Sindrilaru and Scharffetter-Kochanek, 2013 ; Ogle et al., 2016 ; Vishwakarma et al., 2016 ). For example, lipopolysaccharide (LPS), a component of the outer membrane of Gram-negative bacteria, is a PAMP that macrophagesterm·dom recognize via binding with toll-like receptor 4 (Bianchi and Manfredi, 2009 ). This signaling pathway activates the transcription factor, NF-κB, which leads to expression of pro-inflammatory genes. Extracellular DNA, RNA, and ATP, released due to cell death, are examples of DAMPs that signal immune cells and attract them to injury sites (Gallucci, 2016 ). Monocytes can also be recruited to the wound by chemokines and cytokines downstream of DAMPs/PAMPs, such as IL-1, IL-6, TNF-α, and CCL2 (MCP-1), although in mice, CCL3(MIP-1α) and CCL4(MIP-1β) play this role (Evans et al., 2013 ). Multiple monocyte types, categorized as pro-inflammatory and anti-inflammatory, are attracted to the wound site (Ogle et al., 2016 ). The former, sometimes defined as “classical” monocytes, are derived from the bone marrow and spleen, increase in concentration in the bloodstream following injury, and are CD14 + CD16 − (human) or Ly6C +/high (mice) (Ogle et al., 2016 ; Boyette et al., 2017 ). Surface cell adhesion molecules, such as the α 4 β 1 integrin and CD62L, are responsible for recruiting these cells from the circulation to the blood vessel wall. When there is no injury, pro-inflammatory monocytes do not tightly adhere. However, in the vicinity of the wound, the local presence of inflammatory chemokines and cytokines, such as CCL2(MCP-1), TNF-α, and IFN-γ, promotes expression of cell adhesion molecules. This facilitates the firm adhesion of pro-inflammatory monocytes to the endothelium and subsequent translocation into the tissue space. In addition to extravasation, another mechanism of monocyte recruitment to wounds is by entering through micro-hemorrhages in damaged blood vessels (Rodero et al., 2014 ; Minutti et al., 2017 ). With a half-life of only 20 h (in mice), the numbers of pro-inflammatory monocytes fluctuate with the supply of new cells recruited from the bone marrow and circulation, but reach a peak ~48 h after injury (Yona et al., 2013 ; Ogle et al., 2016 ). The second type of recruited monocytes consists of anti-inflammatory monocytes, which have a longer half-life (>2 days, in mice). Human markers include CD14 low/− CD16 + and for mice, Ly6 −/low . These cells attach to the blood vessel wall via α L β 2 integrin (LFA-1) and L-selection (CD62L). The expression of CD62L enables anti-inflammatory monocytes to crawl on the endothelium even during homeostasis, so that they are nearby to aid in tissue and vascular repair when needed (Auffray et al., 2007 ; Ogle et al., 2016 ; Boyette et al., 2017 ). This suggests that, in addition to tissue-resident macrophagesterm·dom, “resident” monocytes may exist as well. Interestingly, pro- and anti-inflammatory monocytes in mice are attracted to areas of inflammationterm·dom via different signals: CCR2 vs. CX3CR1-dependent pathways, respectively (Italiani and Boraschi, 2014 ; Ogle et al., 2016 ). Others have used a different nomenclature to group human monocytes into classical (CD14 ++ CD16 − ), intermediate (CD14 dim CD16 ++ ) and non-classical (CD14 ++ , CD16 + ) phenotypes. The classical phenotype is analogous to the pro-inflammatory phenotype previously described, whereas the non-classical phenotype is analogous to anti-inflammatory monocytes (Boyette et al., 2017 ). Each subset exhibits a different morphology following tissue culture, with classical being the largest and roundest, and non-classical being the smallest and having poor attachment. They each have distinct secretomes and respond to different stimuli to varying degrees. For example, classical and intermediate monocytes readily respond to bacteria-associated signals, whereas non-classical monocytes are much less responsive (Cros et al., 2010 ). All monocyte subsets are capable of differentiating into M1 and M2 macrophagesterm·dom in vitro , however M1 macrophagesterm·dom derived from classical monocytes are the most phagocytic and hence, the “most M1-like” (Boyette et al., 2017 ). Interestingly, non-classical monocytes can differentiate into macrophagesterm·dom even in the absence of differentiation media. This may support one of the proposed models that monocytes themselves transition from classical to non-classical, before differentiating into macrophagesterm·dom (Ogle et al., 2016 ; Boyette et al., 2017 ). So, in addition to the existence of several monocyte phenotypes, each possesses varying potentials to differentiate into different macrophageterm·dom phenotypes as shown through these in vitro studies. This adds further complexity in understanding monocyte recruitment/macrophageterm·dom differentiation in in vivo wound healingterm·dom, where this process is also not entirely clear. In humans, at homeostasis, ~85% of blood monocytes are classical, 5% are intermediate and 10% are non-classical (Italiani and Boraschi, 2014 ). In inflammatory conditions, classical monocytes differentiate into M1-like macrophagesterm·dom whereas non-classical monocytes aid in tissue repair and differentiate into M2-like macrophagesterm·dom (Figure 1 , Process 1). Accordingly, classical monocytes are recruited to wounds to a higher extent following injury compared to non-classical monocytes. There is also evidence that classical monocytes are recruited to the skin for their pro-inflammatory effects, can become non-classical monocytes and eventually differentiate into M2-like macrophagesterm·dom (Crane et al., 2014 ; Ogle et al., 2016 ). With several different monocyte and macrophageterm·dom phenotypes, the recruitment and differentiation processes are complex, especially within dynamic wound microenvironments. It is not surprising that several models of monocyte recruitment and macrophageterm·dom differentiation during injury have arisen. Although not exhaustive, a few widely discussed models are depicted in Figure 1 . Figure 1 Monocyte-Macrophage Recruitment and Differentiation in Wounds. The mechanism of monocyte recruitment and macrophageterm·dom differentiation during dermal wound healingterm·dom can vary depending on spatiotemporal cues. A few models are presented: (1) Classical monocytes in the circulation are primed to differentiate into M1 macrophagesterm·dom following extravasation. In the wound microenvironment, they respond to spatiotemporal cues and can differentiate into any of the M2-like phenotypes, which can transdifferentiate into one another. For brevity, M2a, b, c and d phenotypes are also categorized as M2-like in the remaining processes. (2) Classical monocytes can differentiate into M1 macrophagesterm·dom in the wound. In contrast to the first model, in this panel, macrophagesterm·dom retain the M1 phenotype without further differentiating to M2-like macrophagesterm·dom. Similarly, non-classical monocytes are primed to differentiate into M2-like macrophagesterm·dom and can retain this phenotype. This panel suggests that the final macrophageterm·dom phenotype is predetermined by the starting monocyte phenotype, and an M1/M2 transition does not occur. (3) This model shows that classical monocytes, rather than macrophagesterm·dom, can also persist in the wound environment for several days, and at a later time, differentiate into non-classical monocytes and then M2-like macrophagesterm·dom. Dashes on the blood vessel indicate that monocytes can exit damaged vasculature via micro-hemorrhages. The yellow star-shape represents resident macrophagesterm·dom, which are established during embryonic development. The purple star-shape represents a possible Mhem phenotype in wounds (analogous to that found in atherosclerotic plaques) which breakdowns hemoglobin and releases anti-inflammatory factors. Macrophageterm·dom phenotypes General markers for wound macrophagesterm·dom include CD14 + , FXIIIA + , F4/80 (in mice), CD68 (macrosialin), and lysozyme M (LYZ2). Macrophagesterm·dom can also be identified by their relatively strong autofluorescence, which differentiates them from similar CD14 + monocyte-derived dendritic cells (Njoroge et al., 2001 ; Malissen et al., 2014 ). In general, primary macrophagesterm·dom have limited proliferative capabilities in vitro , although there is evidence that dermal macrophagesterm·dom can self-renew in vivo (Davies et al., 2013 ). In contrast, it is not clear whether monocyte-derived macrophagesterm·dom proliferate in vivo , or if they are simply recruited to the site of injury as needed, and apoptose following healing (Murray and Wynn, 2011 ; Italiani and Boraschi, 2014 ). Furthermore, their proliferative capability may depend on the particular microenvironment or stage of healing (Italiani and Boraschi, 2014 ; Murray, 2017 ). As described in section The General Role of Macrophagesterm·dom in Wound Healingterm·dom, two categories of macrophagesterm·dom have been traditionally defined—classically activated, M1 macrophagesterm·dom and alternatively activated, M2 macrophagesterm·dom . M1 macrophagesterm·dom are typically associated with pro-inflammatory events, whereas M2 macrophagesterm·dom are recognized as anti-inflammatory and pro-regenerative. However, accumulating data suggest that this bipolar M1/M2 definition is grossly oversimplified. It is important to note that M1 and M2 macrophagesterm·dom are not distinct categories, however they form a spectrum in which cells possess varying degrees of M1- or M2-like qualities (Martinez and Gordon, 2014 ). In support of this view, in vivo studies suggest that a heterogeneous population of macrophagesterm·dom exists, with each cell exhibiting a variety of M1 and M2 characteristics (Ogle et al., 2016 ). Some have even described macrophageterm·dom activation as a “color wheel,” with classically-activated, wound healingterm·dom and regulatory macrophagesterm·dom as the primary colors, and the secondary colors representing intermediate macrophageterm·dom phenotypes (Mosser and Edwards, 2008 ). As a result, many additional subpopulations of macrophageterm·dom phenotypes have been described and defined in the literature. Before discussing the specifics of M1- and M2-like macrophagesterm·dom, a different categorization will be presented in section Pro-inflammatory, pro-woundterm·dom Healing and pro-resolving Macrophagesterm·dom—one that separates macrophageterm·dom phenotype based on their role within the wound healingterm·dom process. In regards to this reviewterm·mth, this categorization is more relevant and intuitive, although it is not as widely accepted as the M1/M2 spectrum (section M1/M2 Macrophageterm·dom Spectrum). Discrete M1/M2 phenotypes are useful in vitro when the stimulating molecule is known and experimentally introduced to the system, however this nomenclature is less applicable when discussing in vivo macrophagesterm·dom in a wound healingterm·dom context (Novak and Koh, 2013 ). All of the macrophagesterm·dom associated with wound healingterm·dom across both in vitro and in vivo classification systems are presented in Figure 2 , along with their respective roles. Figure 2 The Role of Macrophageterm·dom Phenotypes in Wound Healingterm·dom. Acute wounds progress through the phases of inflammationterm·dom, proliferation and remodeling as they heal. In inflammationterm·dom , pro-inflammatory macrophagesterm·dom are present. Their role is to phagocytose dead cells and bacteria and prepare the wound for healing. In proliferation , pro-woundterm·dom healing macrophagesterm·dom are present. They secrete factors that aid in angiogenesis, formation of granulation tissue, collagen deposition, and reepithelialization. In remodeling , pro-resolving macrophagesterm·dom aid in breakdown of the provisional granulation tissue to allow for maturation of collagen and strengthening of the newly regenerated skin. Below the diagrams are the general roles and timing of different macrophageterm·dom phenotypes during the wound healingterm·dom process. Differences between in vivo and in vitro classifications are separated by the dashed line, however similar roles can be seen between many of the phenotypes. The timing is an estimate based on the role of each phenotype, and has not been experimentally confirmed. Pro-inflammatory, pro-woundterm·dom healing, and pro-resolving macrophagesterm·dom In agreement with the phases of wound healingterm·dom, pro-inflammatory macrophagesterm·dom are present shortly after a wound is formed, followed by pro-woundterm·dom healing macrophagesterm·dom that support cellular growth and proliferation, and finally pro-resolving macrophagesterm·dom that drastically down-regulate the immune response and aid in collagen reorganization and maturation (Murray and Wynn, 2011 ; Vannella and Wynn, 2017 ). Pro-inflammatory macrophagesterm·dom produce nitric oxide, ROS, IL-1, IL-6, and TNF-α. They also secrete MMP-2 and MMP-9 in order to break down the extracellular matrix and make room for infiltrating inflammatory cells (Murray and Wynn, 2011 ). Pro-woundterm·dom healing macrophagesterm·dom produce elevated levels of growth factors such as PDGF, insulin-like growth factor 1 (IGF-1), VEGF and TGF-β1 (Murray and Wynn, 2011 ; Vannella and Wynn, 2017 ), which aid in cellular proliferation, granulation tissue formation, and angiogenesis. They also produce tissue inhibitor of metalloproteinases 1 (TIMP1) in order to counteract MMPs and allow for ECM formation (Murray and Wynn, 2011 ). Pro-resolving macrophagesterm·dom (aka regulatory macrophagesterm·dom) suppress inflammationterm·dom via upregulation of IL-10. They also express arginase 1, resistin-like molecule-α (RELMα) programmed death ligand 2 (PDL2) and TGF-β1. MMPs (some evidence pointing toward MMP-12 and MMP-13 specifically) are produced to remodel and strengthen the ECM (Hesketh et al., 2017 ; Vannella and Wynn, 2017 ). The function of pro-resolving macrophagesterm·dom is to restore homeostasis while minimizing fibrosis via apoptosis of myofibroblasts, suppression of T cell proliferation and a return to balanced MMP/TIMP levels (Murray and Wynn, 2011 ). Just as wound healingterm·dom phases overlap, these different macrophagesterm·dom also share some characteristics with one another. This is especially true for pro-woundterm·dom healing macrophagesterm·dom which fall between the early and late phases of wound healingterm·dom, and therefore exhibit characteristics similar to both pro-inflammatory and pro-resolving macrophagesterm·dom. M1/M2 macrophageterm·dom spectrum Analogous to pro-inflammatory macrophagesterm·dom, M1 macrophagesterm·dom dominate during the pro-inflammatory phase of wound healingterm·dom, and through their highly phagocytic behavior, serve the role of sanitizing the wound and clearing it of dead tissue. M1 macrophagesterm·dom also activate other immune cells during the early phase of the wound healingterm·dom process. In vitro , M1 macrophagesterm·dom are stimulated by intracellular proteins and nucleic acids released from lysed cells (e.g., IFN- γ), and bacterial components, such as LPS and peptidoglycan (Ferrante and Leibovich, 2012 ). M1 macrophagesterm·dom express CD86, and produce high levels of (ROS) and pro-inflammatory cytokines, such as interleukins 1 and 6 (IL-1, IL-6), TNF- α, and IFN-γ. Traditionally defined M2 macrophagesterm·dom serve a regenerative role. M2 macrophagesterm·dom are stimulated by IL-4 and IL-13 and express high levels of the mannose receptor (CD206), dectin, interleukin 10 (IL-10), and transforming growth factor β (TGF-β). They produce low levels of pro-inflammatory cytokines such as TNF-α, IL-12, and CXCL8(IL-8) (Ferrante and Leibovich, 2012 ). It has also been found that interferon regulator factors (IRF4/IRF5) are transcriptional regulators that play a role in differential signaling seen between M2 and M1 macrophagesterm·dom, respectively. M2 macrophagesterm·dom have been divided into different subtypes according to differential expression of surface markers. These subtypes have been traditionally used and identified in vitro to study M2-like macrophagesterm·dom with different characteristics. In in vivo studies, this nomenclature is not as widely used to identify macrophagesterm·dom, potentially due to the heterogeneous populations present, which are generated from a variety of stimuli within wounds (Novak and Koh, 2013 ). Table 2 identifies the different names and markers for each macrophageterm·dom phenotype. The table is not comprehensive, and it is important to note that marker expression for each phenotype can vary from study to study, hence adding to the complexity and difficulty of defining macrophagesterm·dom. Table 2 Macrophageterm·dom phenotypes and characteristics. Phenotype Other nomenclature Nomenclature by activation molecule Markers Other notes M1 classically activated; pro-inflammatory – Surface: CD86, CD68, CD80, MHC-II Secreted: TNF-α, IL-6, IL-12, IL-1β abundant and persistent in chronic woundsterm·dom; activated in vitro by LPS, peptidoglycans and pro-inflammatory cytokines M2 all M2-phenotypes collectively: alternatively activated; anti-inflammatory – – – M2a alternatively activated; wound healingterm·dom M(IL-4) Surface: CD206, arginase (mice), Ym1 (mice) CD163, MHC-II, CD209 Secreted: TGF-β, IL-10, IL-1RA aid in ECM formation, angiogenesis M2b type 2; regulatory M(Ic) Surface: CD86, MHC-II Secreted: TNF-α, IL-1, IL-6, IL-10 similar to M1 macrophagesterm·dom, but dampen inflammationterm·dom M2c deactivated; pro-resolving? M(IL-10), M(GC), M(GC+TGF-β) Surface: CD86, CD163, CD206 Secreted: IL-10, CD206, TGF-β, MMP-9 involved in vascular and matrix remodeling; some shared characteristics with Mhem M2d – – Secreted: VEGF, IL-10, IL-12, TNF-α, TGF-β pro-angiogenic; activated in vitro by stimulating adenosine and toll-like receptors Mhem HA-Mac; Heme-directed macrophageterm·dom M(Hb) Surface: CD163, CD206 Secreted: IL-10 Internal: HMOX-1 gene, activating transcription factor (ATF) found near hemmorrhaged vessels in atherosclerotic plaques; anti-inflammatory effects M4 CXCL4 derived macrophageterm·dom – Surface: CD206, CD86, Lack CD163 Secreted: IL-6, TNF-α associated with atherosclerosis in human models; M1-like; low phagocytosis Mox Oxidized phospholipid derived macrophagesterm·dom – Surface: ↓arginase-1 Secreted: ↓MCP-1, ↓TNF-α Internal: HMOX-1 gene, HO-1, sulfiridoxin 1, theoredoxin reductase-1 associated with atherosclerosis in murine models; low phagocytosis; antioxidant properties TAMs tumor-associated macrophagesterm·dom – Surface: CD163, CD206, CD204 Secreted: IL-10, MIF, CXCL12, VEGF, IL-6, IL-23, TGF-β Internal: HIF-1α located nearby tumors; promote angiogenesis and cell proliferation; M2-like The previously described M2 macrophagesterm·dom, also known as wound healingterm·dom macrophagesterm·dom, align with what is now defined as the M2a subset (Ogle et al., 2016 ). M2a macrophagesterm·dom are stimulated by IL-4/IL-13 and exhibit IL-4 receptor α (IL-4Rα) signaling (Ferrante and Leibovich, 2012 ). CD206 is a distinguishing surface marker and they produce high levels of arginase-1 (in mice), PDGF-BB, IGF-1, and several chemokines (CCL17, CCL18, CCL22; Ogle et al., 2016 ). M2a macrophagesterm·dom produce collagen precursors and factors that stimulate fibroblasts. Thus, M2a macrophagesterm·dom play a key role in ECM formation, which is required during the proliferative phase of wound healingterm·dom. They also secrete high levels of PDGF, which is involved in angiogenesis (Spiller et al., 2014 ). M2b macrophagesterm·dom, which express CD86, CD68, and MHCII, are stimulated by immune complexes and TLF/Il-1 agonists (Ogle et al., 2016 ; Hesketh et al., 2017 ). They are also known as type 2 macrophagesterm·dom. M2b macrophagesterm·dom suppress inflammationterm·dom by increasing IL-10 production, although they also secrete IL-6, IL-β, and TNF, and express high levels of iNOS. M2b macrophagesterm·dom also produce several different MMPs. In vitro , macrophagesterm·dom take on an M2b phenotype following phagocytosis of apoptotic neutrophils (Filardy et al., 2010 ). M2c macrophagesterm·dom are stimulated by glucocorticoids, IL-10 and TGF-β (Roszer, 2015 ; Garash et al., 2016 ). They express CD206 and MERTK. M2c macrophagesterm·dom produce high levels of IL-10, MMP-9, IL-1β, and TGF-β, and low levels of IL-12. M2c macrophagesterm·dom also express CD163, which is the hemoglobin receptor. This is important to note, as there exists another macrophageterm·dom phenotype, called Mhem, that is similarly characterized by high CD163 expression and IL-10 production, albeit stimulated by hemoglobin and typically identified in atherosclerotic plaques (Boyle, 2012 ). These shared features may indicate that different stimuli can elicit the same, or very similar, macrophageterm·dom phenotypes that are nevertheless referred to by different names (M2c vs. Mhem). Furthermore, due to their production of ECM and MMPs and hence, their matrix remodeling capability, M2c macrophagesterm·dom may be analogous to the aforementioned pro-resolving macrophagesterm·dom. M2c macrophagesterm·dom are also sometimes referred to as deactivated macrophagesterm·dom as they can arise from M1 macrophagesterm·dom that have “deactivated” the M1 gene profile to become M2c macrophagesterm·dom. M2 macrophagesterm·dom can shift between a, b and c phenotypes (Ogle et al., 2016 ). In contrast to M2a macrophagesterm·dom, M2d macrophagesterm·dom do not have either elevated mannose receptor (CD206) or dectin-1 expression (Ferrante and Leibovich, 2012 ). M2d macrophagesterm·dom arise from stimulation by IL-6 and adenosine. They produce high levels of vascular endothelial growth factor (VEGF) as well as IL-10 and TGF-β. They also down-regulate pro-inflammatory TNF-α and IL-12. M2d macrophagesterm·dom are activated by concurrent stimulation of toll-like receptor (via IL-6) and adenosine A 2A receptors (Ferrante and Leibovich, 2012 ; Roszer, 2015 ). Several other macrophageterm·dom types have been defined, however, they tend to be associated with specific diseases, such as atherosclerosis or cancer (Colin et al., 2014 ; Medbury et al., 2014 ). For example, Mox, M4 and Mhem arise from macrophagesterm·dom stimulated by oxidated phospholipids, CXCL4 and hemoglobin-haptoglobin complexes, respectively. Although these phenotypes are not typically associated with chronic woundsterm·dom, it is possible that some wound macrophagesterm·dom have some shared characteristics, especially in regards to Mhem, as hemoglobin-haptoglobin receptor (CD163) expression and cellular regulation of iron are associated with wound healingterm·dom (Cairo et al., 2011 ; Sindrilaru et al., 2011 ; Evans et al., 2013 ). There also exist cancer-specific macrophagesterm·dom, called tumor-associated macrophagesterm·dom (TAMs), which support tumors by stimulating angiogenesis, aiding in metastasis and inhibiting T-cell anti-tumor responses (Yang and Zhang, 2017 ). They can differentiate from resident progenitor cells, but are more often derived from recruited monocytes from the blood stream. TAMs are more similar to M2 macrophagesterm·dom, as they produce anti-inflammatory cytokines and promote proliferation and growth to support the tumor microenvironment. These additional, disease-specific macrophagesterm·dom underline the unique plasticity and range of phenotypes and functions that macrophagesterm·dom possess and can exhibit in different microenvironments. Overall, macrophageterm·dom nomenclature within this vast spectrum is not yet agreed upon and it is unclear whether the phenotypes are distinct, or even applicable to in vivo wound healingterm·dom (Martinez and Gordon, 2014 ). It is important to remember that the macrophageterm·dom population during wound healingterm·dom is complex; wound macrophagesterm·dom can take on a different phenotype depending on several factors, such as the anatomical location of the wound (foot, lower back), the specific region within the wound (center/edge), the environment (moist, dry) and whether or not the wound is infected (Ferrante and Leibovich, 2012 ). Unsurprisingly, it is still unclear the exact signals and differentiation cascade required to produce a specific macrophageterm·dom phenotype (M2a vs. M2b vs. M2c, etc., see Figure 1 ). Adding further complexity to this question is the fact that these phenotypes exist on a spectrum, and macrophagesterm·dom can easily transition from M1-like to M2-like (and M2a-like, M2b-like etc.). Furthermore, wound macrophageterm·dom populations are heterogenous, as it is possible for pro- and anti-inflammatory cytokines to be present simultaneously (Novak and Koh, 2013 ; Martinez and Gordon, 2014 ). Interestingly, although differentiation of M2a macrophagesterm·dom is stimulated by IL-4 and IL-13 in vitro , these cytokines are not present in healing murine wounds that contain M2-like macrophagesterm·dom (Daley et al., 2010 ), further underlining the disconnect between in vitro and in vivo models. Although the defined macrophageterm·dom definitions are useful in vitro , they must be regarded with caution when considering macrophageterm·dom phenotypes in the in vivo wound healingterm·dom process. Macrophageterm·dom standardization efforts Murray et al. ( 2014 ) acknowledge the complexity of the current macrophageterm·dom nomenclature and provide suggestions for improvement moving forward (Murray et al., 2014 ). The authors met to attempt to set a foundation toward consolidating and standardizing the wealth of macrophageterm·dom activation terms and methods that have arisen throughout the years. Their recommendations include: differentiating murine or human bone marrow/peripheral blood monocytes with CSF-1 or GM-CSF to generate macrophagesterm·dom, and using post-differentiation stimuli IFN-γ and IL-4 to obtain M1 and M2 macrophagesterm·dom, respectively; reporting defined metrics such as tissue culture conditions, media, time, etc., to characterize in vitro macrophageterm·dom cultures; defining the activator for in vitro macrophagesterm·dom using the following notation: M(LPS), M(IFN-γ), M (IL-10), etc. and referencing a provided spectrum of M1/M2-like characteristics; the avoidance of the term “regulatory macrophagesterm·dom”, as well as the use of GM-CSF to create M1 macrophagesterm·dom and CSF for M2 macrophagesterm·dom; and use of a combination of markers (cytokines, chemokines, scavenger receptors and more) to describe macrophageterm·dom state. The authors not only discussed how to define in vitro macrophagesterm·dom, but also macrophagesterm·dom isolated from in vivo models. A main point includes encouraging scientists to detail the isolation process in publications. Researchers should also characterize ex vivo macrophagesterm·dom and attempt to fit them within the in vitro macrophageterm·dom spectrum defined in the article, in a manner similar to that depicted in Figure 2 in this reviewterm·mth. They also acknowledge the differences between interspecies macrophagesterm·dom, and suggest thorough side-by-side comparisons in order to glean information about human macrophageterm·dom behavior. With more characterization and understanding, scientists will begin to bridge the gap between macrophagesterm·dom from different sources and species. These guidelines were a vital starting point to tackling the complex challenge of streamlining macrophageterm·dom nomenclature and research/reporting practices. These standards should be broadly distributed, and scientists should regularly meet to update them. As a result, understanding of macrophageterm·dom function and behavior will improve across the entire field. This may prime faster advancement in the development of therapies that target macrophagesterm·dom, within chronic woundterm·dom healing applications and many others. Human vs. murine models Mice are commonly-used animal models for wound healingterm·dom studies due to their affordability and ease-of-use, however, it is important to acknowledge differences between human and murine skin anatomies, wound healingterm·dom processes, and immune systems (and hence, macrophageterm·dom behaviors) (Murray, 2017 ). In terms of anatomy, mice have more densely-packed hair follicles and thinner epidermal and dermal layers compared to human skin (Pasparakis et al., 2014 ). It is also generally believed that murine skin heals by contraction—that is, the edges of the wound pull in toward each other, like a drawstring bag, in order to quickly close. In contrast, human skin heals by re-epithelialization, during which keratinocytes crawl over the granulation tissue in order to close the wound. This assumption has recently been revisited, to argue that mice heal both by contraction and re-epithelialization, making them better models for wound healingterm·dom than previously assumed (Chen et al., 2015 ). Diabetic mice are used as in vivo chronic woundterm·dom models, as they exhibit delayed wound healingterm·dom. Mice are either bred to contain a genetic mutation which results in a diabetes-like phenotype, or it is induced via chemical means, for example, injection with streptozocin (Nunan et al., 2014 ). Diabetic mouse wounds share several key characteristics in common with chronic woundsterm·dom in diabetic patients (Blakytny and Jude, 2006 ). These include decreased nerve count, angiogenesis, granulation tissue formation, and collagen content compared to acute wounds. They both contain higher levels of MMPs and lower levels of TGF-β1, IGF-1, and PDGF. More is actually known about diabetic mouse wounds compared to human diabetic ulcers, due to an increased number of studies and an increased ability to probe and measure tissue characteristics (particularly ex vivo ). So, whereas there are several studies showing decreased VEGF, FGF, and KGF in diabetic mouse wounds, in human diabetic ulcers, there is both an incomplete panel of measured cytokines and growth factors, as well as less significant trends due to large biological variability. One discrepancy between murine and human macrophagesterm·dom is their expression of inducible nitric oxide synthase (iNOS) (Mestas and Hughes, 2004 ). Mouse macrophagesterm·dom readily express iNOS in response to LPS or IFN-γ, and for this reason, it is recognized as an M1 marker in mice. Human macrophagesterm·dom, however, do not over-express iNOS in response to these same stimuli. General markers to identify murine and human macrophagesterm·dom differ as well. In humans, they are CD14 and CD33, and in mice, they are F4/80 and CD11b. Other murine-specific M2 markers include Ym1, FIZZ1, and arginase-1 (Roszer, 2015 ). Human and mouse macrophagesterm·dom also express different FcR and IgG receptors, which play a bigger role in the immune system as a whole, by linking the adaptive and innate immune systems (Mestas and Hughes, 2004 ). The function of specific receptors can also differ between species (Mestas and Hughes, 2004 ). For example, CD163 is a common M2-like macrophageterm·dom marker that functions as the hemoglobin-haptoglobin receptor (Etzerodt et al., 2013 ). In humans, the binding of hemoglobin and haptoglobin significantly increases endocytosis of hemoglobin and activation of downstream signaling pathways. In mice however, haptoglobin does not promote binding of hemoglobin to CD163. Although this may seem insignificant, it is just one specific example of how human and murine macrophagesterm·dom have different mechanisms and behaviors. To overcome these discrepancies, there is a need to conduct thorough, side-by-side experiments (e.g., single-cell and bioinformatics approaches) using monocytes and macrophagesterm·dom from different species and sources (Murray, 2017 ). Through these efforts, well-informed comparisons can be made across models while taking advantage of their other benefits (affordability, ease-of-use, etc.). In addition to specific differences between human and murine skin and macrophagesterm·dom, on a whole, it is important to remember that, although diabetic mice are slower to heal than wild type mice, they do eventually heal. Diabetic mice are not an ideal model for non-healing, chronic woundterm·dom studies, but they do have many fundamental similarities on the tissue and cellular levels, making them a widely-accepted model in current wound healingterm·dom research (Nunan et al., 2014 ). Macrophageterm·dom phenotypes during acute wound healingterm·dom Except for fetal wounds, which have the capacity to regenerate in the absence of inflammatory response, macrophagesterm·dom are vital for successful adult wound healingterm·dom (Leibovich and Ross, 1975 ; Mackool et al., 1998 ). Studies have shown that the depletion of macrophagesterm·dom in wounded mice results in delayed re-epithelialization, reduced collagen formation and impaired angiogenesis (Goren et al., 2009 ; Mirza et al., 2009 ). These effects occurred along with increased levels of TNF-α and decreased VEGF and TGF-β1. Furthermore, in the absence of macrophagesterm·dom, there was a prolonged neutrophil presence and reduced wound contraction (Goren et al., 2009 ). Although the general importance of macrophagesterm·dom in wound healingterm·dom is known, there is still much to learn about the details regarding timing, relative proportion and specific role of each phenotype. Mirza and Koh ( 2011 ) isolated macrophagesterm·dom during the wound healingterm·dom process in mice at Days 5, 10, and 20 post-injury in order to study the temporal phenotype change (Mirza and Koh, 2011 ). In wild type mice, pro-inflammatory macrophagesterm·dom were detected on Day 5. These macrophagesterm·dom expressed high levels of IL-1β, MMP-9, and nitric oxide synthase (NOS). By Day 10, the expression of these pro-inflammatory factors decreased, concurrent with an increase in expression of anti-inflammatory markers CD206 and CD36 and growth factors IGF-1, TGF-β, and VEGF. Non-diabetic mice had efficient wound repair, achieving wound closure after 20 days, at which elevated expression remained for CD206, CD36, and TGF-β, but not for IGF-1 or VEGF. Evans et al. ( 2013 ) used an acute wound model in humans to better understand the pro- to anti- inflammatory macrophageterm·dom transition in blisters (Evans et al., 2013 ). Wounds were chemically induced by application of cantharidin, a topical treatment for warts. Blister fluid was collected 16 and 40 h after injury, to represent the inflammatory and resolving phases of wound healingterm·dom, respectively. Cell counts from the fluid yielded more monocytes/macrophagesterm·dom at the 40 h time point compared to 16 h. Furthermore, the proportion of CD163+ macrophagesterm·dom increased over 10 fold at the later time point (3.4 vs. 47.6%), indicating that CD163 is strongly associated with the resolution phase of healing. Amounts of inflammatory mediators were also measured in the wound fluid. At the 16 h “inflammatory” time point, there were significantly higher levels of CCL2(MCP-1), CXCL8(IL-8), TNF-α, CCL3(MIP-1α), CCL4(MIP-1β), and CCL11(eotaxin). At the 40 h “resolution” time point, there was significantly more macrophage-derived chemokine (MDC) and TGF-β in the wound fluid. Interestingly, this study reported undetectable levels of IL-10 at either time point, which is surprising, as it is recognized as a cytokine produced at high levels by anti-inflammatory macrophagesterm·dom. Macrophageterm·dom dysregulation and chronic woundsterm·dom When macrophagesterm·dom become dysregulated, several wound healingterm·dom complications can arise, such as the formation of chronic woundsterm·dom or excessive scarring (Vannella and Wynn, 2017 ). Macrophagesterm·dom in chronic woundsterm·dom have a reduced capability to phagocytose dead neutrophils, which, as a result, accumulate and promote a strong inflammatory environment. Diabetic patients have macrophagesterm·dom with reduced apoptotic clearance activity because of the effects of hyperglycemia and advanced glycation endproducts (Khanna et al., 2010 ; Hesketh et al., 2017 ). The act of neutrophil clearance by macrophagesterm·dom can induce the phenotypic switch of M1 macrophagesterm·dom to M2b, and lead to the resolution of inflammationterm·dom (Filardy et al., 2010 ; Hesketh et al., 2017 ). This is one of many reasons as to why chronic woundsterm·dom may have an abundance of M1 macrophagesterm·dom. Significantly higher numbers of macrophagesterm·dom are found in the peripheries of venous and diabetic ulcers compared to acute wounds (Loots et al., 1998 ). In this study, CD68 was used as a general marker to detect macrophagesterm·dom (although other studies define it as an M1 marker, this study did not make that clear). In acute wounds, the number of macrophagesterm·dom was highest at the first time point, and decreased as healing progressed. In contrast, venous and diabetic ulcers had the highest number of macrophagesterm·dom compared to acute wounds. The results of this study also suggested that macrophagesterm·dom are not the only immune cell that is dysregulated in chronic woundterm·dom healing, as lower numbers of T-cells and higher numbers of B-cells were also observed. Another study also detected high levels of CD68 macrophagesterm·dom in the dermis and wound edges in chronic leg ulcers (Moore et al., 1997 ). CD16 and CD35 were also measured and defined as “activation-associated markers,” with positive staining denoting the presence of mature macrophagesterm·dom (rather than monocytes) in inflammatory environments. Most of the wounds studied had low expression of these markers (<12%), and the few areas that were positive were near the vasculature, suggesting that other microenvironments in the wound suppress or prevent macrophageterm·dom activation. Although this study provided information about macrophageterm·dom presence and marker expression in chronic woundsterm·dom, particularly in different locations of a single wound, a low patient number (12 patients) was evaluated and results were not compared relative to patients with acute wounds. These early studies provided important histological data on macrophagesterm·dom in human wounds, but did not explicitly discriminate between pro- or anti-inflammatory phenotypes, nor did they measure cytokines or growth factors in the wound environment. Most in vivo studies, especially in humans, do not tend to study macrophagesterm·dom directly via detection of cell markers, but rather indirectly through the cytokines and proteins present in the wound tissue or fluid. Macrophagesterm·dom are major producers of cytokines and growth factors during wound healingterm·dom, so, based on the identities and amounts measured, a determination can be made on whether the local macrophageterm·dom population is more pro- or anti-inflammatory (M1/M2-like). Accordingly, studies show that chronic woundterm·dom fluid contains high levels of pro-inflammatory cytokines, particularly TNF-α and IL-1β, which were measured to be 100-fold higher compared to acute wounds fluids (mastectomy drain fluids; Tarnuzzer and Schultz, 1996 ). IL-6 was also elevated, but only 2–4 fold. In contrast, mastectomy fluid had the highest levels IL-1β and IL-6 on Day 1 post-surgery and thereby steadily decreased to Day 7. Interestingly, TNF-α levels remained constant during this time period. This is in agreement with observations by Wallace and Stacey, who also observed higher levels of total TNF-α in chronic woundsterm·dom (Wallace and Stacey, 1998 ). Interestingly, the amount of bioactive TNF-α in both healing and non-healing wounds was not significantly different. The amount of bioactive TNF-α did not change as acute wounds closed, suggesting that the regulation of other cytokines may be more important in progressing wound healingterm·dom. Chronic woundterm·dom fluid also contains high levels of MMPs, specifically MMP-2 and MMP-9 (Wysocki et al., 1993 ). MMPs degrade proteins and extracellular matrix and are not favorable for extended periods, as they do not support tissue regrowth in the proliferative phase of wound healingterm·dom. Macrophagesterm·dom produce MMPs, so they may be responsible for maintaining elevated levels in chronic woundsterm·dom (Newby, 2008 ). Specifically, human blood monocytes are stimulated to produce MMP-2 and MMP-9 in the presence of pro-inflammatory signals, such as LPS, IFN-γ, IL-1β, and TNF-α (Zhou et al., 2003 ; Newby, 2008 ). Furthermore, the proteases degrade and decrease the bioactivity of growth factors that may be present, hence canceling out their pro-healing benefits as inflammationterm·dom prevails (Tarnuzzer and Schultz, 1996 ). Since there are no non-healing animal models of chronic woundsterm·dom, diabetic mice are often used as they exhibit delayed wound healingterm·dom and share several characteristics with human chronic woundsterm·dom (Blakytny and Jude, 2006 ; Nunan et al., 2014 ). Studies investigating wound macrophagesterm·dom show that their function is not properly regulated in diabetic vs. wild type mice, with a prolonged M1 macrophageterm·dom presence and hence, inefficient transition to the M2 phenotype (Mirza and Koh, 2011 ). Mirza and Koh found that, although macrophagesterm·dom from non-diabetic mouse wounds had transitioned from a pro- to anti-inflammatory phenotype by Day 10, macrophagesterm·dom from diabetic mice retained pro-inflammatory characteristics. This included two-fold higher levels of pro-inflammatory factors IL-1β and IFN-γ, and ~two-fold lower anti-inflammatory IL-10 in the general wound environment. More specifically, isolated macrophagesterm·dom from Day 10 wounds in diabetic vs. non-diabetic mice had significantly higher mRNA expression of IL-1β and MMP-9 and significantly lower expression of CD206 and CD36. At the same time, they have reduced growth factor production (IGF-1, TGF-β1, VEGF, and IL-10). In non-diabetic wounds, these factors are already present and contributing to key events in wound healingterm·dom such as cell proliferation and migration, ECM formation, and angiogenesis. Most of the aforementioned cytokine and growth factor trends were retained until Day 20, which is in stark contrast to non-diabetic wounds, which had already healed by this point and long-completed the M1-to-M2 transition. Also interesting to note, is the fact that diabetic wounds contained fewer mature macrophagesterm·dom (more Ly6C expression v. F4/80) even at Day 10, suggesting that the monocyte-to-macrophage transition is impaired and may contribute to delayed wound healingterm·dom. Overall, diabetic and non-diabetic wound macrophagesterm·dom only started to exhibit significantly different cytokine/growth factor differences by Day 10; at Day 5, they had similar levels. This suggests that between Day 5 and Day 10, non-diabetic mouse wounds are transitioning to the proliferative phase, in accordance with the M1 to M2-like macrophageterm·dom phenotype change. Diabetic mouse wounds remain highly inflammatory, guided by persistent pro-inflammatory macrophagesterm·dom. Overall, this study provided key evidence of delayed macrophageterm·dom phenotype transition concurrent with delayed wound healingterm·dom in diabetic mice. Other studies have shown prolonged presence of other pro-inflammatory cytokines in diabetic mouse wounds, much longer than seen in wild type mice. One study compared the expression of IL-1β and TNF-α in three different mouse strains: Balb/c, C57BLKS, and db/db (Wetzler et al., 2000 ). No IL-1β was detected after Day 7 in the first two strains, whereas high levels persisted into Day 13 in diabetic mouse wounds. Similarly, TNF-α was detected at the highest levels in db/db mouse wounds at Day 13, and was completely absent or present at very low levels in the wild type groups at the same time. The diabetic group also retained elevated levels of MIP-2 and CCL2(MCP-1) mRNA and protein into Day 13, whereas both strains of wild type mice had stopped producing those factors by Day 13 or even earlier. MIP-2 and CCL2(MCP-1) are chemoattractants, so their presence continually attracted more macrophagesterm·dom, which was detrimental to healing, as the macrophagesterm·dom that were recruited maintained an M1 phenotype. Again, the prolonged presence of pro-inflammatory/M1 macrophagesterm·dom is a hallmark of delayed wound healingterm·dom in diabetic mice. Differential iron regulation by macrophagesterm·dom is another factor that can promote M1/M2 phenotypes (Cairo et al., 2011 ). M1-like cells store the majority of the iron intracellularly as ferritin, whereas, M2-like macrophagesterm·dom release it to the extracellular environment via the transmembrane channel, ferroportin. Sindrilaru et al. ( 2011 ) identified the role of high intracellular iron stores in maintaining M1 macrophagesterm·dom in chronic woundsterm·dom, particularly chronic venous ulcers (Sindrilaru et al., 2011 ). The source of iron was hemoglobin from erythrocytes that escape from damaged blood vessels and enter the wound environment. In a corresponding wounded murine model with iron delivered intravenously, wound macrophagesterm·dom produced high levels of TNF and hydroxyl radical, and a senescence program was induced in nearby fibroblasts. As a result, wound closure was delayed. The prolonged presence of the M1 phenotype is not the only macrophage-related problem that can contribute to wound healingterm·dom disruption. In fact, if M2-like macrophagesterm·dom remain for too long, there may be excessive collagen formation, resulting in scarring (Sindrilaru and Scharffetter-Kochanek, 2013 ; Vannella and Wynn, 2017 ). It is interesting to note that fetal wound healingterm·dom is scarless, with virtually no infiltrating macrophagesterm·dom, and many have attempted to mimic this model to improve wound healingterm·dom outcomes in adults (Mackool et al., 1998 ). These examples suggest that an overabundance or prolonged presence of macrophagesterm·dom, regardless of the phenotype, can lead to wound healingterm·dom complications. Experimental therapies and wound macrophagesterm·dom Based on the role played by the different types of macrophagesterm·dom in the wound healingterm·dom response, it has been hypothesized that interventions that dampen the M1 macrophageterm·dom phenotype and promote M2-like characteristics may help the healing of chronic woundsterm·dom. Some have even delivered exogenous macrophagesterm·dom as cell therapies for chronic woundsterm·dom. A few of these approaches are highlighted below and summarized in Table 3 . Note that the table focuses on key in vivo studies, whereas the text in the following subsections includes both in vivo and in vitro results. Table 3 Experimental approaches to modulate macrophagesterm·dom in wound healingterm·dom. Method Wound model Treatment details Conclusion