Regeneration of corneal epithelium utilizing a collagen vitrigel membrane in rabbit models for corneal stromal wound and limbal stem cell deficiency

被引:41
|
作者
Chae, J. Jeremy [1 ,2 ]
Ambrose, Winnette McIntosh [1 ,2 ]
Espinoza, Freddy A. [1 ,2 ]
Mulreany, Daniel G. [1 ,2 ]
Ng, Shengyong [1 ,2 ]
Takezawa, Toshiaki [3 ]
Trexler, Morgana M. [4 ]
Schein, Oliver D. [5 ]
Chuck, Roy S. [6 ]
Elisseeff, Jennifer H. [1 ,2 ,5 ]
机构
[1] Johns Hopkins Univ, Wilmer Eye Inst, Translat Tissue Engn Ctr, Baltimore, MD 21231 USA
[2] Johns Hopkins Univ, Dept Biomed Engn, Baltimore, MD 21231 USA
[3] Natl Inst Agrobiol Sci, Div Anim Sci, Tsukuba, Ibaraki, Japan
[4] Johns Hopkins Univ, Appl Phys Lab, Res & Exploratory Dev Dept, Laurel, MD USA
[5] Johns Hopkins Univ, Dept Ophthalmol, Baltimore, MD 21231 USA
[6] Montefiore Med Ctr, Albert Einstein Coll Med, Dept Ophthalmol, Bronx, NY 10467 USA
基金
美国国家科学基金会;
关键词
cell transplantation; collagen vitrigel; corneal epithelium; corneal wound; fibrin glue; limbal stem cell deficiency; OCULAR SURFACE RECONSTRUCTION; IN-SITU KERATOMILEUSIS; AMNIOTIC MEMBRANE; FIBRIN GLUE; BIOLOGICAL RESPONSE; GENE-EXPRESSION; TRANSPLANTATION; INGROWTH; TISSUE; VITRO;
D O I
10.1111/aos.12503
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: This study was performed to evaluate the potential of a collagen-based membrane, collagen vitrigel (CV), for reconstructing corneal epithelium in the stromal wound and limbal stem cell deficiency (LSCD) models. Methods: Three groups of rabbits were used in the stromal wound model: CV affixed using fibrin glue (CV + FG group, n = 9), fibrin glue only (FG group, n = 3) and an untreated control group (n = 3). In the LSCD model, one group received CV containing human limbal epithelial cells (CV + hLEC group, n = 2) and the other was an untreated control (n = 1). Gross observation, including fluorescent staining, pathological examination, immunohistochemistry and electron microscopy, was used to evaluate the effect of CV on the corneal epithelium. Results: In the stromal wound model, fluorescent staining showed that epithelial reconstruction occurred as rapidly in the CV + FG group as it did in the control group. The pathological examination proved that the CV supported a healthy corneal epithelium in the CV + FG group, whereas FG led to hypertrophy and inappropriate differentiation of corneal epithelium in the FG group. In the LSCD model, the corneas in the CV + hLEC group showed sustained tissue transparency with good epithelialization, low inflammatory response and reduced neovascularization. However, the control cornea was translucent and showed high amounts of inflammation and neovascularization. Conclusion: We have demonstrated that CV supports corneal epithelial differentiation and prevents epithelial hypertrophy, in addition to serving as a scaffold for hLEC transplantation, without complications.
引用
收藏
页码:E57 / E66
页数:10
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