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透射电子显微镜分析兔角膜混浊时上皮基底膜的修复。

Transmission electron microscopy analysis of epithelial basement membrane repair in rabbit corneas with haze.

机构信息

Cole Eye Institute, Cleveland Clinic, Cleveland, OH 44195, USA.

出版信息

Invest Ophthalmol Vis Sci. 2013 Jun 10;54(6):4026-33. doi: 10.1167/iovs.13-12106.

Abstract

PURPOSE

To assess the ultrastructure of the epithelial basement membrane using transmission electron microscopy (TEM) in rabbit corneas with and without subepithelial stroma opacity (haze).

METHODS

Two groups of eight rabbits each were included in this study. Photorefractive keratectomy (PRK) was performed using an excimer laser. The first group had -4.5-diopter (-4.5D) PRK and the second group had -9.0D PRK. Contralateral eyes were unwounded controls. Rabbits were sacrificed at 4 weeks after surgery. Immunohistochemical analysis was performed to detect the myofibroblast marker α-smooth muscle actin (SMA). TEM was performed to analyze the ultrastructure of the epithelial basement membrane and stroma.

RESULTS

At 4 weeks after PRK, α-SMA+ myofibroblasts were present at high density in the subepithelial stroma of rabbit eyes that had -9.0D PRK, along with prominent disorganized extracellular matrix, whereas few myofibroblasts and little disorganized extracellular matrix were noted in eyes that had -4.5D PRK. The epithelial basement membrane was irregular and discontinuous and lacking typical morphology in all corneas at 1 month after -9D PRK compared to corneas at 1 month in the -4.5D PRK group.

CONCLUSIONS

The epithelial basement membrane acts as a critical modulator of corneal wound healing. Structural and functional defects in the epithelial basement membrane correlate to both stromal myofibroblast development from precursor cells and continued myofibroblast viability, likely through the modulation of epithelial-stromal interactions mediated by cytokines. Prolonged stromal haze in the cornea is associated with abnormal regeneration of the epithelial basement membrane.

摘要

目的

使用透射电子显微镜(TEM)评估兔角膜上皮基底膜的超微结构,这些角膜有或无上皮下基质混浊(混浊)。

方法

本研究纳入两组各 8 只兔子。使用准分子激光行光折射性角膜切削术(PRK)。第一组行-4.5 屈光度(-4.5D)PRK,第二组行-9.0D PRK。对侧眼为未受伤对照眼。术后 4 周处死兔子。行免疫组织化学分析以检测肌成纤维细胞标志物α-平滑肌肌动蛋白(SMA)。行 TEM 分析以分析上皮基底膜和基质的超微结构。

结果

PRK 术后 4 周,行-9.0D PRK 的兔眼上皮下基质中可见高密度的α-SMA+肌成纤维细胞,伴有明显的细胞外基质紊乱,而行-4.5D PRK 的兔眼则仅可见少量肌成纤维细胞和少量紊乱的细胞外基质。与 -4.5D PRK 组 1 个月时的角膜相比,行-9D PRK 后 1 个月所有角膜的上皮基底膜均不规则、不连续且缺乏典型形态。

结论

上皮基底膜是角膜伤口愈合的关键调节因子。上皮基底膜的结构和功能缺陷与前体细胞来源的基质肌成纤维细胞的发育以及肌成纤维细胞的持续存活相关,这可能是通过细胞因子介导的上皮-基质相互作用的调节所致。角膜基质混浊持续存在与上皮基底膜的异常再生相关。

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