Can we produce a human corneal equivalent by tissue engineering?

被引:102
作者
Germain, L
Carrier, P
Auger, FA
Salesse, C
Guérin, SL
机构
[1] Lab Organogenese Expt, Quebec City, PQ G1S 4L8, Canada
[2] Univ Laval, Dept Chirurg, Ste Foy, PQ G1K 7P4, Canada
[3] CHU Laval, Ctr Rech, Unite Rech Ophtalmol, Quebec City, PQ G1V 4G2, Canada
[4] CHU Laval, Ctr Rech, Mol Endocrinol Lab, Quebec City, PQ G1V 4G2, Canada
基金
英国医学研究理事会;
关键词
D O I
10.1016/S1350-9462(00)00005-7
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Tissue engineering is progressing rapidly. Bioengineered substitutes are already available for experimental applications and some clinical purposes such as skin replacement. This review focuses on the development of reconstructed human cornea in vitro by tissue engineering. Key elements to consider in the corneal reconstruction, such as the source for epithelial cells and keratocytes. are discussed and the various steps of production are presented. Since one application of this human model is ro obtain a better understanding of corneal wound healing, the mechanisms of this phenomenon as well as the function played both by membrane-bound integrins and components from the extracellular matrix have also been addressed. The analysis of integrins by immunohistofluorescence labelling of our reconstructed human cornea revealed that beta(1), alpha(3), alpha(5), and alpha(6) integrin subunits were expressed but alpha(4) was not. Laminin. type VII collagen and fibronectin were also detected. Finally, the future challenges of corneal reconstruction by tissue engineering are discussed and the tremendous applications of such tissue produced in vitro for experimental as well as clinical purposes are considered, (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:497 / 527
页数:31
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