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Epha2 在细胞迁移和眼球晶状体屈光组织中的作用。

A role for epha2 in cell migration and refractive organization of the ocular lens.

机构信息

Department of Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, Missouri 63110, USA.

出版信息

Invest Ophthalmol Vis Sci. 2012 Feb 1;53(2):551-9. doi: 10.1167/iovs.11-8568.

Abstract

PURPOSE

The Epha2 receptor is a surprisingly abundant component of the membrane proteome of vertebrate lenses. In humans, genetic studies have linked mutations in EPHA2 to inherited and age-related forms of cataract, but the function of Epha2 in the lens is obscure. To gain insights into the role of Epha2, a comparative analysis of lenses from wild-type and Epha2(-/-) mice was performed.

METHODS

Epha2 distribution was examined using immunocytochemistry and Western blot analysis. Lens optical quality was assessed by laser refractometry. Confocal microscopy was used to analyze cellular phenotypes.

RESULTS

In wild-type lenses, Epha2 was expressed by lens epithelial cells and elongating fibers but was degraded during the later stages of fiber differentiation. Epha2-null lenses retained their transparency, but two key optical parameters, lens shape and internal composition, were compromised in Epha2(-/-) animals. Epha2-null lenses were smaller and more spherical than age-matched wild-type lenses, and laser refractometry revealed a significant decrease in refractive power of the outer cell layers of mutant lenses. In the absence of Epha2, fiber cells deviated from their normal course and terminated at sutures that were no longer centered on the optical axis. Patterning defects were also noted at the level of individual cells. Wild-type fiber cells had hexagonal cross-sectional profiles with membrane protrusions extending from the cell vertices. In contrast, Epha2(-/-) cells had irregular profiles, and protrusions extended from all membrane surfaces.

CONCLUSIONS

These studies indicate that Epha2 is not required for transparency but does play an indispensable role in the cytoarchitecture and refractive quality of the lens.

摘要

目的

Epha2 受体是脊椎动物晶状体膜蛋白组中出乎意料的丰富成分。在人类中,遗传研究将 EPHA2 中的突变与遗传性和年龄相关性白内障联系起来,但 Epha2 在晶状体中的功能尚不清楚。为了深入了解 Epha2 的作用,对野生型和 Epha2(-/-) 小鼠的晶状体进行了比较分析。

方法

使用免疫细胞化学和 Western blot 分析检查 Epha2 的分布。通过激光折射仪评估晶状体光学质量。共聚焦显微镜用于分析细胞表型。

结果

在野生型晶状体中,Epha2 由晶状体上皮细胞和伸长纤维表达,但在纤维分化的后期阶段被降解。Epha2 缺失的晶状体保持透明,但两个关键的光学参数,晶状体形状和内部组成,在 Epha2(-/-) 动物中受到损害。Epha2 缺失的晶状体比同龄野生型晶状体小且更球形,激光折射仪显示突变体晶状体外层细胞的折射力显著降低。在没有 Epha2 的情况下,纤维细胞偏离了它们的正常轨迹,并在不再位于光轴中心的缝合处终止。在单个细胞的水平上也注意到了图案缺陷。野生型纤维细胞具有从细胞顶点延伸的膜突起的六边形横截面轮廓。相比之下,Epha2(-/-)细胞具有不规则的轮廓,并且突起从所有膜表面延伸。

结论

这些研究表明,Epha2 不是透明所必需的,但在晶状体的细胞结构和折射质量中发挥不可或缺的作用。

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