Tissue-engineered human skin substitutes developed from collagen-populated hydrated gels: clinical and fundamental applications

被引:88
作者
Auger, FA [1 ]
Rouabhia, M [1 ]
Goulet, F [1 ]
Berthod, F [1 ]
Moulin, V [1 ]
Germain, L [1 ]
机构
[1] Univ Laval, Dept Chirurg, CHA, Lab Organogenese Expt, Quebec City, PQ G1K 7P4, Canada
关键词
tissue engineering; skin; skin equivalent; collagen; collagen gels;
D O I
10.1007/BF02518887
中图分类号
TP39 [计算机的应用];
学科分类号
081203 ; 0835 ;
摘要
The field of tissue engineering has opened several avenues in biomedical sciences, through ongoing progress. Skin substitutes are currently optimised for clinical as well as fundamental applications. The paper reviews the development of collagen-populated hydrated gels for their eventual use as a therapeutic option for the treatment of burn patients or chronic wounds: tools for pharmacological and toxicological studies, and cutaneous models for in vitro studies. These skin substitutes are produced by culturing keratinocytes on a matured dermal equivalent composed of fibroblasts included in a collagen gel. New biotechnological approaches have been developed to prevent contraction (anchoring devices) and promote epithelial cell differentiation. The impact of dermo-epidermal interactions on the differentiation and organisation of bio-engineered skin tissues has been demonstrated with human skin cells. Human skin substitutes have been adapted for percutaneous absorption studies and toxicity assessment. The evolution of these human skin substitutes has been monitored in vivo in preclinical studies showing promising results. These substitutes could also serve as in vitro models for better understanding of the immunological response and healing mechanism in human skin. Thus, such human skin substitutes present various advantages and are leading to the development of other bio-engineered tissues, such as blood vessels, ligaments and bronchi.
引用
收藏
页码:801 / 812
页数:12
相关论文
共 178 条
  • [111] Paquet I, 1996, J CELL PHYSIOL, V166, P296, DOI 10.1002/(SICI)1097-4652(199602)166:2<296::AID-JCP7>3.0.CO
  • [112] 2-K
  • [113] PAQUETTE JS, 1998, CAN RESP, V5, P1
  • [114] THE ORGANOTYPIC CULTURE OF HUMAN SKIN KERATINOCYTES AND FIBROBLASTS TO ACHIEVE FORM AND FUNCTION
    PARENTEAU, NL
    BILBO, P
    NOLTE, CJM
    MASON, VS
    ROSENBERG, M
    [J]. CYTOTECHNOLOGY, 1992, 9 (1-3) : 163 - 171
  • [115] EPIDERMIS GENERATED INVITRO - PRACTICAL CONSIDERATIONS AND APPLICATIONS
    PARENTEAU, NL
    NOLTE, CM
    BILBO, P
    ROSENBERG, M
    WILKINS, LM
    JOHNSON, EW
    WATSON, S
    MASON, VS
    BELL, E
    [J]. JOURNAL OF CELLULAR BIOCHEMISTRY, 1991, 45 (03) : 245 - 251
  • [116] FIRST-ORDER TOXICITY ASSAYS FOR EYE IRRITATION USING CELL-LINES - PARAMETERS THAT AFFECT IN-VITRO EVALUATION
    PASTERNAK, AS
    MILLER, WM
    [J]. FUNDAMENTAL AND APPLIED TOXICOLOGY, 1995, 25 (02): : 253 - 263
  • [117] PETERSEN MJ, 1987, J BIOL CHEM, V262, P835
  • [118] ASCORBIC-ACID AND TRANSFORMING GROWTH FACTOR-BETA-1 INCREASE COLLAGEN BIOSYNTHESIS VIA DIFFERENT MECHANISMS - COORDINATE REGULATION OF PRO-ALPHA-1(I) AND PRO-ALPHA-1(III) COLLAGENS
    PHILLIPS, CL
    TAJIMA, S
    PINNELL, SR
    [J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1992, 295 (02) : 397 - 403
  • [119] Phillips T J, 1990, Adv Dermatol, V5, P33
  • [120] CULTURED EPIDERMAL AUTOGRAFTS AND ALLOGRAFTS - A STUDY OF DIFFERENTIATION AND ALLOGRAFT SURVIVAL
    PHILLIPS, TJ
    BHAWAN, J
    LEIGH, IM
    BAUM, HJ
    GILCHREST, BA
    [J]. JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1990, 23 (02) : 189 - 198