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Role of Wdr45b in maintaining neural autophagy and cognitive function,Autophagy, 25 Jun 2019
2019-06-25 | 【     】【打印】【关闭

Autophagy25 June, 2019,DOI:https://doi.org/10.1080/15548627.2019.1632621

Role of Wdr45b in maintaining neural autophagy and cognitive function

Cuicui Ji, Hongyu Zhao, Dongfang Li, Huayu Sun, Junfeng Hao, Ruiguo Chen, Xiaoqun Wang, Hong Zhang & Yan G Zhao

Abstract

Macroautophagy/autophagy functions as a quality control mechanism by degrading misfolded proteins and damaged organelles and plays an essential role in maintaining neural homeostasis. The phosphoinositide phosphatidylinositol-3-phosphate (PtdIns3P) effector Atg18 is essential for autophagosome formation in yeast. Mammalian cells contain four Atg18 homologs, belonging to two subclasses, WIPI1 (WD repeat domain, phosphoinositide interacting 1), WIPI2 and WDR45B/WIPI3 (WD repeat domain 45B), WDR45/WIPI4. The role of Wdr45b in autophagy and in neural homeostasis, however, remains unknown. Recent human genetic studies have revealed a potential causative role of WDR45B in intellectual disability. Here we demonstrated that mice deficient in Wdr45b exhibit motor deficits and learning and memory defects. Histological analysis reveals that wdr45b knockout (KO) mice exhibit a large number of swollen axons and show cerebellar atrophy. SQSTM1- and ubiquitin-positive aggregates, which are autophagy substrates, accumulate in various brain regions in wdr45b KO mice. Double KO mice, wdr45b and wdr45, die within one day after birth and exhibit more severe autophagy defects than either of the single KO mice, suggesting that these two genes act cooperatively in autophagy. Our studies demonstrated that WDR45B is critical for neural homeostasis in mice. The wdr45b KO mice provide a model to study the pathogenesis of intellectual disability.

文章链接:https://www.tandfonline.com/doi/full/10.1080/15548627.2019.1632621

 

 

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