Open AccessA synapsin Ⅰ cleavage fragment contributes to synaptic dysfunction in Alzheimer's disease
Author(s) -
Meng Lanxia,
Zou Li,
Xiong Min,
Chen Jiehui,
Zhang Xingyu,
Yu Ting,
Li Yiming,
Liu Congcong,
Chen Guiqin,
Wang Zhihao,
Ye Keqiang,
Zhang Zhentao
Publication year - 2022
Publication title -
aging cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.103
H-Index - 140
eISSN - 1474-9726
pISSN - 1474-9718
DOI - 10.1111/acel.13619
Subject(s) - synapsin , synapsin i , biology , neuroscience , hippocampus , synaptic plasticity , synaptophysin , calpain , synaptic fatigue , excitatory postsynaptic potential , biochemistry , immunology , synaptic vesicle , receptor , inhibitory postsynaptic potential , enzyme , immunohistochemistry , vesicle , membrane
Synaptic dysfunction is a key feature of Alzheimer's disease (AD). However, the molecular mechanisms underlying synaptic dysfunction remain unclear. Here, we show that synapsin Ⅰ, one of the most important synaptic proteins, is fragmented by the cysteine proteinase asparagine endopeptidase (AEP). AEP cleaves synapsin at N82 in the brains of AD patients and generates the C‐terminal synapsin Ⅰ (83–705) fragment. This fragment is abnormally distributed in neurons and induces synaptic dysfunction. Overexpression of AEP in the hippocampus of wild‐type mice results in the production of the synapsin Ⅰ (83–705) fragment and induces synaptic dysfunction and cognitive deficits. Moreover, overexpression of the AEP‐generated synapsin Ⅰ (83–705) fragment in the hippocampus of tau P301S transgenic mice and wild‐type mice promotes synaptic dysfunction and cognitive deficits. These findings suggest a novel mechanism of synaptic dysfunction in AD.