The inflammation-fibrosis link? A Jekyll and Hyde role for blood cells during wound repair

被引:185
作者
Stramer, Brian M.
Mori, Ryoichi
Martin, Paul
机构
[1] Univ Bristol, Sch Med Sci, Dept Physiol, Bristol BS8 1TD, Avon, England
[2] Univ Bristol, Sch Med Sci, Dept Biochem, Bristol BS8 1TD, Avon, England
基金
英国医学研究理事会;
关键词
D O I
10.1038/sj.jid.5700811
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
The healing of a skin wound is a complex process involving many cell lineages. In adult tissues, repair is always accompanied by a robust inflammatory response, which is necessary to counter the potential for infection at any site where the skin barrier is breached. Unlike embryonic tissues that can repair perfectly without a remnant scar at the wound site, adult tissue repair always leads to formation of a fibrotic scar where the wound has healed. In recent years, it has become clear that the wound inflammatory response may be, at least in part, responsible for fibrosis at sites of tissue repair. In this review, we consider the beneficial vs the detrimental functions of inflammatory cells during the repair response and compare data from other tissues, the lung, and liver, where fibrosis and its resolution may be related to a damage-triggered inflammatory response. We also consider how it may be possible to molecularly disentangle the potentially good from the bad influences of inflammatory cells during tissue repair and how fundamental studies in inflammatory cell biology may prove the way forward for development of drug targets in this respect.
引用
收藏
页码:1009 / 1017
页数:9
相关论文
共 82 条
[1]   Peripheral blood fibrocytes: Differentiation pathway and migration to wound sites [J].
Abe, R ;
Donnelly, SC ;
Peng, T ;
Bucala, R ;
Metz, CN .
JOURNAL OF IMMUNOLOGY, 2001, 166 (12) :7556-7562
[2]  
ADAMSON IYR, 1988, AM J PATHOL, V130, P377
[3]  
ADZICK NS, 1985, J PEDIATR SURG, V20, P315
[4]   SCARLESS FETAL HEALING - THERAPEUTIC IMPLICATIONS [J].
ADZICK, NS ;
LONGAKER, MT .
ANNALS OF SURGERY, 1992, 215 (01) :3-7
[5]  
Aiba S, 1997, J CUTAN PATHOL, V24, P65
[6]   CD34+ SPINDLE-SHAPED CELLS SELECTIVELY DISAPPEAR FROM THE SKIN LESION OF SCLERODERMA [J].
AIBA, S ;
TABATA, N ;
OHTANI, H ;
TAGAMI, H .
ARCHIVES OF DERMATOLOGY, 1994, 130 (05) :593-597
[7]   THE SEVERE AND MODERATE PHENOTYPES OF HERITABLE MAC-1, LFA-1 DEFICIENCY - THEIR QUANTITATIVE DEFINITION AND RELATION TO LEUKOCYTE DYSFUNCTION AND CLINICAL-FEATURES [J].
ANDERSON, DC ;
SCHMALSTEIG, FC ;
FINEGOLD, MJ ;
HUGHES, BJ ;
ROTHLEIN, R ;
MILLER, LJ ;
KOHL, S ;
TOSI, MF ;
JACOBS, RL ;
WALDROP, TC ;
GOLDMAN, AS ;
SHEARER, WT ;
SPRINGER, TA .
JOURNAL OF INFECTIOUS DISEASES, 1985, 152 (04) :668-689
[8]   PLATELET-DERIVED GROWTH-FACTOR IN IDIOPATHIC PULMONARY FIBROSIS [J].
ANTONIADES, HN ;
BRAVO, MA ;
AVILA, RE ;
GALANOPOULOS, T ;
NEVILLEGOLDEN, J ;
MAXWELL, M ;
SELMAN, M .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (04) :1055-1064
[9]   INJURY INDUCES INVIVO EXPRESSION OF PLATELET-DERIVED GROWTH-FACTOR (PDGF) AND PDGF RECEPTOR MESSENGER-RNAS IN SKIN EPITHELIAL-CELLS AND PDGF MESSENGER-RNA IN CONNECTIVE-TISSUE FIBROBLASTS [J].
ANTONIADES, HN ;
GALANOPOULOS, T ;
NEVILLEGOLDEN, J ;
KIRITSY, CP ;
LYNCH, SE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (02) :565-569
[10]   ONTOGENY OF THE SKIN AND THE TRANSITION FROM SCAR-FREE TO SCARRING PHENOTYPE DURING WOUND-HEALING IN THE POUCH YOUNG OF A MARSUPIAL, MONODELPHIS-DOMESTICA [J].
ARMSTRONG, JR ;
FERGUSON, MWJ .
DEVELOPMENTAL BIOLOGY, 1995, 169 (01) :242-260