Mechanisms of wound reepithelialization: hints from a tissue-engineered reconstructed skin to long-standing questions

被引:155
作者
Laplante, AF [1 ]
Germain, L [1 ]
Auger, FA [1 ]
Moulin, V [1 ]
机构
[1] Univ Laval, Dept Surg, CHA Quebec, Hop St Sacrement,LOEX, Quebec City, PQ G1S 4L8, Canada
关键词
wound healing; keratinocyte; epithelia; drug screening;
D O I
10.1096/fj.01-0250com
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Wound closure of epithelial tissues must occur efficiently to restore rapidly their barrier function. We have developed a tissue-engineered wound-healing model composed of human skin keratinocytes and fibroblasts to better understand the mechanisms of reepithelialization. It allowed us to quantify the reepithelialization rate, which was significantly accelerated in the presence of fibrin or platelet-rich plasma. The reepithelialization of these 6 mm excisional wounds required the contribution of keratinocyte proliferation, migration, stratification, and differentiation. The epidermis regenerated progressively from the surrounding wound margins. After 3 days, the neoepidermis showed a complete spectrum of changes. Near the wound margin, the differentiation of the neoepidermis (keratins 1/10, filaggrin, and loricrin) and regeneration of the dermoepidermal junction (laminin 5 and collagen IV) were more advanced than toward the wound center, where the proliferative index was significantly increased. The spatial distribution of keratinocytes distinguished by particular features suggests two complementary mechanisms of reepithelialization: 1) the passive displacement of the superficial layers near the wound margin that would rapidly regenerate a barrier function and 2) the crawling of keratinocytes over each other at the tip of the progressing neoepidermis. Therefore, this study brings a new perspective to long-standing questions concerning wound reepithelialization.
引用
收藏
页码:2377 / 2389
页数:13
相关论文
共 64 条
[1]   ROLE AND INNOCUITY OF TISSEEL(R), A TISSUE GLUE, IN THE GRAFTING PROCESS AND INVIVO EVOLUTION OF HUMAN CULTURED EPIDERMIS [J].
AUGER, FA ;
GUIGNARD, R ;
VALLE, CAL ;
GERMAIN, L .
BRITISH JOURNAL OF PLASTIC SURGERY, 1993, 46 (02) :136-142
[2]   LIVING TISSUE FORMED INVITRO AND ACCEPTED AS SKIN-EQUIVALENT TISSUE OF FULL THICKNESS [J].
BELL, E ;
EHRLICH, HP ;
BUTTLE, DJ ;
NAKATSUJI, T .
SCIENCE, 1981, 211 (4486) :1052-1054
[3]   THE TIME-DEPENDENT LOCALIZATION OF KI67 ANTIGEN-POSITIVE CELLS IN HUMAN SKIN WOUNDS [J].
BETZ, P ;
NERLICH, A ;
WILSKE, J ;
TUBEL, J ;
PENNING, R ;
EISENMENGER, W .
INTERNATIONAL JOURNAL OF LEGAL MEDICINE, 1993, 106 (01) :35-40
[4]   In vitro reconstruction of a human capillary-like network in a tissue-engineered skin equivalent [J].
Black, AF ;
Berthod, F ;
L'Heureux, N ;
Germain, L ;
Auger, FA .
FASEB JOURNAL, 1998, 12 (13) :1331-1340
[5]  
BUCK RC, 1979, INVEST OPHTH VIS SCI, V18, P767
[6]   DISTINCTIVE INTEGRIN EXPRESSION IN THE NEWLY FORMING EPIDERMIS DURING WOUND-HEALING IN HUMANS [J].
CAVANI, A ;
ZAMBRUNO, G ;
MARCONI, A ;
MANCA, V ;
MARCHETTI, M ;
GIANNETTI, A .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1993, 101 (04) :600-604
[7]   FIBRONECTIN AND FIBRIN PROVIDE A PROVISIONAL MATRIX FOR EPIDERMAL-CELL MIGRATION DURING WOUND REEPITHELIALIZATION [J].
CLARK, RAF ;
LANIGAN, JM ;
DELLAPELLE, P ;
MANSEAU, E ;
DVORAK, HF ;
COLVIN, RB .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1982, 79 (05) :264-269
[8]  
COHEN IK, 1994, PRINCIPLES SURG, P279
[9]   The 'ins' and 'outs' of intermediate filament organization [J].
Coulombe, PA ;
Bousquet, O ;
Ma, LL ;
Yamada, S ;
Wirtz, D .
TRENDS IN CELL BIOLOGY, 2000, 10 (10) :420-428
[10]  
Dale B. A., 1994, KERATINOCYTE HDB, P323