Tissue engineering of cultured skin substitutes

被引:195
作者
Horch, RE [1 ]
Kopp, J [1 ]
Kneser, U [1 ]
Beier, J [1 ]
Bach, AD [1 ]
机构
[1] Univ Erlangen Nurnberg, Dept Plast & Hand Surg, D-91054 Erlangen, Germany
关键词
skin substitutes; keratinocyte culture; massive burns; tissue engineering; fibrin sealant; biological matrices; monolayers; collagen; hyaluronic acid; allografts;
D O I
10.1111/j.1582-4934.2005.tb00491.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Skin replacement has been a challenging task for surgeons ever since the introduction of skin grafts by Reverdin in 1871. Recently, skin grafting has evolved from the initial autograft and allograft preparations to biosynthetic and tissue-engineered living skin replacements. This has been fostered by the dramatically improved survival rates of major burns where the availability of autologous normal skin for grafting has become one of the limiting factors. The ideal properties of a temporary and a permanent skin substitute have been well defined. Tissue-engineered skin replacements: cultured autologous keratinocyte grafts, cultured allogeneic keratinocyte grafts, autologous/allogeneic composites, acellular biological matrices, and cellular matrices including such biological substances as fibrin sealant and various types of collagen, hyaluronic acid etc. have opened new horizons to deal with such massive skin loss. In extensive burns it has been shown that skin substitution with cultured grafts can be a life-saving measure where few alternatives exist. Future research will aim to create skin substitutes with cultured epidermis that under appropriate circumstances may provide a wound cover that could be just as durable and esthetically acceptable as conventional split-thickness skin grafts. Genetic manipulation may in addition enhance the performance of such cultured skin substitutes. If cell science, molecular biology, genetic engineering, material science and clinical expertise join their efforts to develop optimized cell culture techniques and synthetic or biological matrices then further technical advances might well lead to the production of almost skin like new tissue-engineered human skin products resembling natural human skin.
引用
收藏
页码:592 / 608
页数:17
相关论文
共 150 条
[1]  
Achauer B M, 1985, Crit Care Clin, V1, P47
[2]   Etoposide differentially affects bone marrow and dermal derived endothelial cells [J].
Adams, SW ;
Wang, L ;
Fortney, J ;
Gibson, LF .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2004, 8 (03) :338-348
[3]   Generation of recombinant skin in vitro by adeno-associated virus type 2 vector transduction [J].
Agrawal, N ;
You, H ;
Liu, Y ;
Chiriva-Internati, M ;
Bremner, J ;
Garg, T ;
Grizzi, F ;
Prasad, CK ;
Mehta, JL ;
Hermonat, PL .
TISSUE ENGINEERING, 2004, 10 (11-12) :1707-1715
[4]  
ALEXANDER JW, 1981, J TRAUMA, V21, P433
[5]   IN SEARCH OF AN IDEAL SKIN SUBSTITUTE [J].
ALSBJORN, B .
SCANDINAVIAN JOURNAL OF PLASTIC AND RECONSTRUCTIVE SURGERY AND HAND SURGERY, 1984, 18 (01) :127-133
[6]   Composition and characteristics of an autologous thrombocyte gel [J].
Altmeppen, J ;
Hansen, E ;
Bonnländer, GL ;
Horch, RE ;
Jeschke, MG .
JOURNAL OF SURGICAL RESEARCH, 2004, 117 (02) :202-207
[7]   Gene transfer to epidermal stem cells: implications for tissue engineering [J].
Andreadis, ST .
EXPERT OPINION ON BIOLOGICAL THERAPY, 2004, 4 (06) :783-800
[8]   Plasmid gene delivery to human keratinocytes through a fibrin-mediated transfection system [J].
Andree, C ;
Voigt, M ;
Wenger, A ;
Erichsen, T ;
Bittner, K ;
Schaefer, D ;
Walgenbach, KJ ;
Borges, J ;
Horch, RE ;
Eriksson, E ;
Stark, B .
TISSUE ENGINEERING, 2001, 7 (06) :757-766
[9]   In search of adult renal stem cells [J].
Anglani, F ;
Forino, M ;
Del Prete, D ;
Tosetto, E ;
Torregrossa, R ;
D'Angelo, A .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2004, 8 (04) :474-487
[10]   KERATINOCYTES AND FIBROBLASTS IN A HUMAN SKIN EQUIVALENT MODEL ENHANCE MELANOCYTE SURVIVAL AND MELANIN SYNTHESIS AFTER ULTRAVIOLET-IRRADIATION [J].
ARCHAMBAULT, M ;
YAAR, M ;
GILCHREST, BA .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1995, 104 (05) :859-867