Loss of ephrin-A5 function disrupts lens fiber cell packing and leads to cataract

被引:98
作者
Cooper, Margaret A. [1 ]
Son, Alexander I. [1 ]
Komlos, Daniel [2 ]
Suna, Yuhai [1 ]
Kleiman, Norman J. [3 ]
Zhou, Renping [1 ]
机构
[1] Rutgers State Univ, Ernest Mario Sch Pharm, Susan Lehman Cullman Lab Canc Res, Dept Biol Chem, Piscataway, NJ 08854 USA
[2] Robert Wood Johnson Med Sch, Dept Neurosci & Cell Biol, Piscataway, NJ 08854 USA
[3] Columbia Univ, Mailman Sch Publ Hlth, Dept Environm Hlth Sci, New York, NY 10032 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
beta-catenin; Eph receptor; N-cadherin;
D O I
10.1073/pnas.0808987105
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cell-cell interactions organize lens fiber cells into highly ordered structures to maintain transparency. However, signals regulating such interactions have not been well characterized. We report here that ephrin-A5, a ligand of the Eph receptor tyrosine kinases, plays a key role in lens fiber cell shape and cell-cell interactions. Lens fiber cells in mice lacking ephrin-A5 function appear rounded and irregular in cross-section, in contrast to their normal hexagonal appearance in WT lenses. Cataracts eventually develop in 87% of ephrin-A5 KO mice. We further demonstrate that ephrin-A5 interacts with the EphA2 receptor to regulate the adherens junction complex by enhancing recruitment of beta-catenin to N-cadherin. These results indicate that the Eph receptors and their ligands are critical regulators of lens development and maintenance.
引用
收藏
页码:16620 / 16625
页数:6
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