内体
谷氨酸的
加巴能
内吞循环
突触小泡
生物发生
生物
神经科学
细胞生物学
神经传递
突触囊泡循环
谷氨酸受体
小泡
生物化学
内吞作用
抑制性突触后电位
细胞
受体
基因
细胞内
膜
作者
Xia Li,Liming Qin,Yefei Li,Hao Yu,Zhi‐Jun Zhang,Chang-Lu Tao,Yijun Liu,Yanhong Xue,Xiaoxing Zhang,Zhenghao Xu,Yi Wang,Huifang Lou,Zhibin Tan,Paul Säftig,Zhong Chen,Tao Xu,Guo‐Qiang Bi,Shumin Duan,Zhihua Gao
出处
期刊:Cell Reports
[Elsevier]
日期:2019-07-01
卷期号:28 (4): 1015-1028.e5
被引量:22
标识
DOI:10.1016/j.celrep.2019.06.006
摘要
Presynaptic endosomes reportedly participate in synaptic vesicle (SV) recycling. However, it remains unclear whether they differentially regulate SV biogenesis and synaptic transmission in different types of synapses and how they are implicated in diseases. Using cryo-electron tomography and endocytic tracing, we uncover different endocytic modes and dynamics associated with distinct SV morphology between glutamatergic and GABAergic synapses. We further find that cathepsin D (CatD), a lysosomal storage disease (LSD) protein, is selectively located in GABAergic presynaptic endosomes. Inactivation of CatD results in enlarged presynaptic endosomes, reduces the readily releasable pool, and impairs synaptic transmission in GABAergic, but not glutamatergic, synapses. Moreover, CatD-deficient mice exhibit hyperactivity and increased sensitivity to seizure, mimicking epileptic behavior in CatD-related LSD patients. These data reveal an important role for presynaptic endosomal CatD in regulating GABAergic SV biogenesis and provide mechanistic insights for understanding the synaptic pathology and behavioral defects in CatD-associated LSD.
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