The use of PEGT/PBT as a dermal scaffold for skin tissue engineering

被引:64
作者
El Ghalbzouri, A
Lamme, EN
van Blitterswijk, C
Koopman, J
Ponec, M
机构
[1] Leiden Univ, Med Ctr, Dept Dermatol, Sylvius Lab, NL-2300 RA Leiden, Netherlands
[2] Isotis NV, Bilthoven, Netherlands
[3] Profibrix, Leiderdorp, Netherlands
关键词
skin tissue engineering; fibrin; fibroblast; keratinocyte; dermal substitute; keratin; basement membrane;
D O I
10.1016/j.biomaterials.2003.09.098
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Human skin equivalents (HSEs) were engineered using biodegradable-segmented copolymer PEGT/PBT as a dermal scaffold. As control groups, fibroblast-populated de-epidermized dermis, collagen, fibrin and hybrid PEGT/PBT-collagen matrices were used. Two different approaches were used to generate full-thickness HSE. In the 1-step approach, keratinocytes were seeded onto the fibroblast-populated scaffolds and cultured at the air-liquid (A/L) interface. In the 2-step approach, fully differentiated epidermal sheets were transferred onto fibroblast-populated scaffolds and cultured at the A/L. In a 1-step procedure, keratinocytes migrated into the porous PEGT/PBT scaffold. This was prevented by incorporating fibroblast-populated collagen into the pores of the PEGT/PBT matrix or using the 2-step procedure. Under all experimental conditions, fully differentiated stratified epidermis and basement membrane was formed. Differences in K6, K16, K17, collagen type VII, laminin 5 and nidogen staining were observed. In HSE generated with PEGT/PBT, the expression of these keratins was higher, and the deposition of collagen type VII, laminin 5 and nidogen at the epidermal/matrix junction was retarded compared to control HSEs. Our results illustrate that the copolymer PEGT/ PBT is a suitable scaffold for the 2-step procedure, whereas the incorporation of fibroblast-populated collagen or fibrin into the pores of the scaffold is required for the 1-step procedure. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2987 / 2996
页数:10
相关论文
共 44 条
[31]  
PONEC M, 1988, J LIPID RES, V29, P949
[32]   Keratinocytes contract human dermal extracellular matrix and reduce soluble fibronectin production by fibroblasts in a skin composite model [J].
Ralston, DR ;
Layton, C ;
Dalley, AJ ;
Boyce, SG ;
Freedlander, E ;
MacNeil, S .
BRITISH JOURNAL OF PLASTIC SURGERY, 1997, 50 (06) :408-415
[33]   Correlation between hyperproliferation and suprabasal integrin expression in human epidermis reconstituted in culture [J].
Rikimaru, K ;
Moles, JP ;
Watt, FM .
EXPERIMENTAL DERMATOLOGY, 1997, 6 (05) :214-221
[34]   The acidic milieu of the horny layer: New findings on the physiology and pathophysiology of skin pH [J].
Rippke F. ;
Schreiner V. ;
Schwanitz H.-J. .
American Journal of Clinical Dermatology, 2002, 3 (4) :261-272
[35]   Burn wound healing and skin substitutes [J].
Shakespeare, P .
BURNS, 2001, 27 (05) :517-522
[36]   Recent clinical experience with cultured autologous epithelium [J].
Sheridan, RL ;
Tompkins, RG .
BRITISH JOURNAL OF PLASTIC SURGERY, 1996, 49 (01) :72-74
[37]   CULTURED AUTOLOGOUS EPITHELIUM IN PATIENTS WITH BURNS OF 90-PERCENT OR MORE OF THE BODY-SURFACE [J].
SHERIDAN, RL ;
TOMPKINS, RG .
JOURNAL OF TRAUMA-INJURY INFECTION AND CRITICAL CARE, 1995, 38 (01) :48-50
[38]   MUTUAL INDUCTION OF GROWTH-FACTOR GENE-EXPRESSION BY EPIDERMAL-DERMAL CELL-INTERACTION [J].
SMOLA, H ;
THIEKOTTER, G ;
FUSENIG, NE .
JOURNAL OF CELL BIOLOGY, 1993, 122 (02) :417-429
[39]   Organotypic keratinocyte cocultures in defined medium with regular epidermal morphogenesis and differentiation [J].
Stark, HJ ;
Baur, M ;
Breitkreutz, D ;
Mirancea, N ;
Fusenig, NE .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1999, 112 (05) :681-691
[40]  
Van Dorp AGM, 1999, WOUND REPAIR REGEN, V7, P214