Development of an in vitro burn wound model

被引:58
作者
Coolen, Neeltje A. [1 ,2 ]
Vlig, Marcel [1 ]
van den Bogaerdt, Antoon J. [1 ]
Middelkoop, Esther [1 ,2 ]
Ulrich, Magda M. W. [1 ,2 ]
机构
[1] Assoc Dutch Burn Ctr, NL-1940 EA Beverwijk, Netherlands
[2] Vrije Univ Amsterdam Med Ctr, Dept Plast Reconstruct & Hand Surg, Amsterdam, Netherlands
关键词
D O I
10.1111/j.1524-475X.2008.00403.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
Healing of a deeper burn wound is a complex process that often leads to scar formation. Skin wound model systems are important for the development of treatments preventing scarring. The aim of this study is to develop a standardized in vitro burn wound model that resembles the in vivo situation. A burn wound (10 x 2 mm) was made in ex vivo skin and the skin samples were cultured at the air-liquid interface for 7, 14, and 21 days. Cells in the skin biopsies maintained their viability during the 21-day culture period. During culture, reepithelialization of the wound took place from the surrounding tissue and fibroblasts migrated into the wound area. Cells of the epithelial tongue and fibroblasts near the wound margin were proliferating. During culture, skin-derived antileukoproteinase and keratin 17 were expressed only in the epithelial tongue. Both collagen type IV and laminin were present underneath the newly formed epidermis, indicating that the basement membrane was restored. These results show that the burn wound model has many similarities to in vivo wound healing. This burn wound model may be useful to study different aspects of wound healing and testing pharmaceuticals and cosmetics on, e.g., migration and reepithelialization.
引用
收藏
页码:559 / 567
页数:9
相关论文
共 32 条
[1]
Comparison of wound closure after burn and cold injury in human skin equivalents [J].
Breetveld, Melanie ;
Richters, Cornelia D. ;
Rustemeyer, Thomas ;
Scheper, Rik J. ;
Gibbs, Susan .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2006, 126 (08) :1918-1921
[2]
Increased proliferation in keloid fibroblasts wounded in vitro [J].
Calderon, M ;
Lawrence, WT ;
Banes, AJ .
JOURNAL OF SURGICAL RESEARCH, 1996, 61 (02) :343-347
[3]
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
[4]
Enhanced modulation of keratinocyte motility by transforming growth factor-alpha (TGF-alpha) relative to epidermal growth factor (EGF) [J].
Cha, D ;
OBrien, P ;
OToole, EA ;
Woodley, DT ;
Hudson, LG .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1996, 106 (04) :590-597
[5]
A standardized model of partial thickness scald burns in mice [J].
Cribbs, RK ;
Luquette, MH ;
Besner, GE .
JOURNAL OF SURGICAL RESEARCH, 1998, 80 (01) :69-74
[6]
Differential cutaneous wound healing in thermally injured MRL/MPJ mice [J].
Davis, Thomas A. ;
Amare, Mihret ;
Naik, Shruti ;
Kovalchuk, Alexander L. ;
Tadaki, Douglas .
WOUND REPAIR AND REGENERATION, 2007, 15 (04) :577-588
[7]
DEVRIES HJC, 1995, BRIT J DERMATOL, V132, P690
[8]
Accelerated wound closure in neutrophil-depleted mice [J].
Dovi, JV ;
He, LK ;
DiPietro, LA .
JOURNAL OF LEUKOCYTE BIOLOGY, 2003, 73 (04) :448-455
[9]
ORGAN-CULTURE OF HUMAN SKIN IN CHEMICALLY DEFINED MEDIUM [J].
FLAXMAN, BA ;
HARPER, RA .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1975, 64 (02) :96-99
[10]
Keratins and the keratinocyte activation cycle [J].
Freedberg, IM ;
Tomic-Canic, M ;
Komine, M ;
Blumenberg, M .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2001, 116 (05) :633-640