Macrophages in skin injury and repair

被引:590
作者
Delavary, Babak Mahdavian [1 ,2 ]
van der Veer, Willem M. [1 ,2 ]
van Egmond, Marjolein [1 ,3 ]
Niessen, Frank B. [2 ]
Beelen, Robert H. J. [1 ]
机构
[1] Vrije Univ Amsterdam Med Ctr, Dept Mol Cell Biol & Immunol, Amsterdam, Netherlands
[2] Vrije Univ Amsterdam Med Ctr, Dept Plast & Reconstruct Surg, Amsterdam, Netherlands
[3] Vrije Univ Amsterdam Med Ctr, Dept Surg, Amsterdam, Netherlands
关键词
Inflammation; Macrophages; Phenotype; Remodelling; Skin; Wound healing; ENDOTHELIAL GROWTH-FACTOR; BLOOD-VESSEL GROWTH; WOUND REPAIR; EXTRACELLULAR-MATRIX; ALTERNATIVE ACTIVATION; HYPERTROPHIC SCARS; TGF-BETA; IN-VITRO; CELLS; ANGIOGENESIS;
D O I
10.1016/j.imbio.2011.01.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
After recruitment to the wound bed, monocytes differentiate into macrophages. Macrophages play a central role in all stages of wound healing and orchestrate the wound healing process. Their functional phenotype is dependent on the wound microenvironment, which changes during healing, hereby altering macrophage phenotype. During the early and short inflammatory phase macrophages exert pro-inflammatory functions like antigen-presenting, phagocytosis and the production of inflammatory cytokines and growth factors that facilitate the wound healing process. As such, the phenotype of wound macrophages in this phase is probably the classically activated or the so-called M1 phenotype. During the proliferative phase, macrophages stimulate proliferation of connective, endothelial and epithelial tissue directly and indirectly. Especially fibroblasts, keratinocytes and endothelial cells are stimulated by macrophages during this phase to induce and complete ECM formation, reepithelialization and neovascularization. Subsequently, macrophages can change the composition of the ECM both during angiogenesis and in the remodelling phase by release of degrading enzymes and by synthesizing ECM molecules. This suggests an important role for alternatively activated macrophages in this phase of wound healing. Pathological functioning of macrophages in the wound healing process can result in derailed wound healing, like the formation of ulcers, chronic wounds, hypertrophic scars and keloids. However, the exact role of macrophages in these processes is still incompletely understood. For treating wound repair disorders more should be elucidated on the role of macrophages in these conditions, especially their functional phenotype, to find more therapeutic opportunities. This review summarizes macrophage function in skin injury repair, thereby providing more insight in macrophage function in wound healing and possible interventions in this process. (C) 2011 Elsevier GmbH. All rights reserved.
引用
收藏
页码:753 / 762
页数:10
相关论文
共 83 条
[21]   REGULATION OF VASCULAR ENDOTHELIAL GROWTH-FACTOR EXPRESSION IN CULTURED KERATINOCYTES - IMPLICATIONS FOR NORMAL AND IMPAIRED WOUND-HEALING [J].
FRANK, S ;
HUBNER, G ;
BREIER, G ;
LONGAKER, MT ;
GREENHALGH, DG ;
WERNER, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (21) :12607-12613
[22]   Other functions, other genes: Alternative activation of antigen-presenting cells [J].
Goerdt, S ;
Orfanos, CE .
IMMUNITY, 1999, 10 (02) :137-142
[23]   INDUCTION OF MACROPHAGE PLASMINOGEN ACTIVATOR BY ENDOTOXIN STIMULATION AND PHAGOCYTOSIS - EVIDENCE FOR A 2-STAGE PROCESS [J].
GORDON, S ;
UNKELESS, JC ;
COHN, ZA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1974, 140 (04) :995-1010
[24]   Alternative activation of macrophages [J].
Gordon, S .
NATURE REVIEWS IMMUNOLOGY, 2003, 3 (01) :23-35
[25]   Alternatively activated macrophages differentially express fibronectin and its splice variants and the extracellular matrix protein βIG-H3 [J].
Gratchev, A ;
Guillot, P ;
Hakiy, N ;
Politz, O ;
Orfanos, CE ;
Schledzewski, K ;
Goerdt, S .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 2001, 53 (04) :386-392
[26]   PROLIFERATIVE RESPONSE INVITRO OF VASCULAR ENDOTHELIAL AND SMOOTH-MUSCLE CELLS EXPOSED TO WOUND FLUIDS AND MACROPHAGES [J].
GREENBURG, GB ;
HUNT, TK .
JOURNAL OF CELLULAR PHYSIOLOGY, 1978, 97 (03) :353-360
[27]   Wound repair and regeneration [J].
Gurtner, Geoffrey C. ;
Werner, Sabine ;
Barrandon, Yann ;
Longaker, Michael T. .
NATURE, 2008, 453 (7193) :314-321
[28]   The direct thrombin inhibitors (argatroban, bivalirudin and lepirudin) and the indirect Xa-inhibitor (danaparoid) increase fibrin network porosity and thus facilitate fibrinolysis [J].
He, Shu ;
Blomback, Margareta ;
Bark, Niklas ;
Johnsson, Hans ;
Wallen, N. Hakan .
THROMBOSIS AND HAEMOSTASIS, 2010, 103 (05) :1076-1084
[29]   Normoxic wound fluid contains high levels of vascular endothelial growth factor [J].
Howdieshell, TR ;
Riegner, C ;
Gupta, V ;
Callaway, D ;
Grembowicz, K ;
Sathyanarayana ;
McNeil, PL .
ANNALS OF SURGERY, 1998, 228 (05) :707-715
[30]   Synthetic TGF-β antagonist accelerates wound healing and reduces scarring [J].
Huang, JS ;
Wang, YH ;
Ling, TY ;
Chuang, SS ;
Johnson, FE ;
Huang, SS .
FASEB JOURNAL, 2002, 16 (08) :1269-+