Deletion of prominin-1 in mice results in disrupted photoreceptor outer segment protein homeostasis

小鼠中 prominin-1 的缺失导致感光外节蛋白质稳态紊乱

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作者:Yu-Shu Xiao, Jian Liang, Min Gao, Jun-Ran Sun, Yang Liu, Jie-Qiong Chen, Xiao-Huan Zhao, Yi-Min Wang, Yu-Hong Chen, Yu-Wei Wang, Xiao-Ling Wan, Xue-Ting Luo, Xiao-Dong Sun

Aim

To illustrate the underlying mechanism how prominin-1 (also known as Prom1) mutation contribute to progressive photoreceptor degeneration.

Conclusion

Prom1 deprivation causes progressive photoreceptor degeneration. Prom1 is essential for maintaining normal trafficking and normal quantity of photoreceptor OS proteins. The new light is shed on the pathogenic mechanism underlying photoreceptor degeneration caused by Prom1 mutation.

Methods

A CRISPR-mediated Prom1 knockout (Prom1-KO) mice model in the C57BL/6 was generated and the photoreceptor degeneration phenotypes by means of structural and functional tests were demonstrated. Immunohistochemistry and immunoblot analysis were performed to reveal the localization and quantity of related outer segment (OS) proteins.

Results

The Prom1-KO mice developed the photoreceptor degeneration phenotype including the decreased outer nuclear layer (ONL) thickness and compromised electroretinogram amplitude. Immunohistochemistry analysis revealed impaired trafficking of photoreceptor OS proteins. Immunoblot data demonstrated decreased photoreceptor OS proteins.

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