高尔基体
神经退行性变
细胞生物学
甾醇调节元件结合蛋白
胶质增生
神经突
基因剔除小鼠
生物
调节器
生物化学
化学
胆固醇
甾醇
内质网
内科学
神经科学
体外
基因
医学
疾病
作者
Yu‐shin Sou,Junji Yamaguchi,Hiroshi Kameda,Keisuke Masuda,Yusuke Maeda,Yasuo Uchiyama,Masato Koike
出处
期刊:FEBS Letters
[Wiley]
日期:2022-09-03
卷期号:596 (22): 2873-2888
标识
DOI:10.1002/1873-3468.14491
摘要
The Golgi pH regulator (GPHR) is essential for maintaining the function and morphology of the Golgi apparatus through the regulation of luminal acidic pH. Abnormal morphology of the Golgi apparatus is associated with neurodegenerative diseases. Here, we found that knockout of GPHR in the mouse brain led to morphological changes in the Golgi apparatus and neurodegeneration, which included brain atrophy, neuronal cell death, and gliosis. Furthermore, in the GPHR knockout mouse brain, transcriptional activity of sterol regulatory element-binding protein 2 (SREBP2) decreased, resulting in a reduction in cholesterol levels. GPHR-deficient cells exhibited suppressed neurite outgrowth, which was recovered by exogenous expression of the active form of SREBP2. Our results show that GPHR-mediated luminal acidification of the Golgi apparatus maintains proper cholesterol levels and, thereby, neuronal morphology.
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