4.4 Article

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

期刊

ACTA OPHTHALMOLOGICA
卷 93, 期 1, 页码 E57-E66

出版社

WILEY-BLACKWELL
DOI: 10.1111/aos.12503

关键词

cell transplantation; collagen vitrigel; corneal epithelium; corneal wound; fibrin glue; limbal stem cell deficiency

资金

  1. Congressionally Directed Medical Research Program under U.S. Army Medical Research and Materiel Command [W81XWH-09-2-0173]
  2. Research to Prevent Blindness (RPB) Foundation
  3. RPB
  4. National Science Foundation Graduate Research Fellowship
  5. UNCF-Merck Graduate Dissertation fellowship
  6. Mokam Scientific Foundation

向作者/读者索取更多资源

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.

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