慢性不可预测压力诱导成体海马神经干细胞自噬死亡

IF 3.3 3区 医学 Q2 NEUROSCIENCES Molecular Brain Pub Date : 2024-06-03 DOI:10.1186/s13041-024-01105-6
Seongwon Choe, Hyeonjeong Jeong, Jieun Choi, Seong-Woon Yu
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引用次数: 0

摘要

慢性心理压力是焦虑症、痴呆症和抑郁症等神经系统并发症的关键因素。我们之前的研究结果表明,慢性束缚应激通过诱导成体海马神经干细胞(NSCs)的自噬死亡,导致认知障碍和情绪失调。然而,其他心理应激模型是否也会诱导成年海马神经干细胞自噬性死亡尚不清楚。在这里,我们发现持续10天的慢性不可预知应激(CUS)会损害小鼠的记忆功能并增加焦虑。SOX2和KI67的免疫组化染色显示,暴露于CUS后海马中的NSCs数量显著减少。然而,NSC特异性诱导性条件性缺失Atg7可以防止这些缺陷。这些研究结果表明,成年海马NSCs的自噬死亡是应激诱导的脑部疾病的一个关键致病机制。
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Chronic unpredictable stress induces autophagic death of adult hippocampal neural stem cells.

Chronic psychological stress is a critical factor for neurological complications like anxiety disorders, dementia, and depression. Our previous results show that chronic restraint stress causes cognitive deficits and mood dysregulation by inducing autophagic death of adult hippocampal neural stem cells (NSCs). However, it is unknown whether other models of psychological stress also induce autophagic death of adult hippocampal NSCs. Here, we show that chronic unpredictable stress (CUS) for 10 days impaired memory function and increased anxiety in mice. Immunohistochemical staining with SOX2 and KI67 revealed a significant reduction in the number of NSCs in the hippocampus following exposure to CUS. However, these deficits were prevented by NSC-specific, inducible conditional deletion of Atg7. These findings suggest that autophagic death of adult hippocampal NSCs is a critical pathogenic mechanism underlying stress-induced brain disorders.

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来源期刊
Molecular Brain
Molecular Brain NEUROSCIENCES-
CiteScore
7.30
自引率
0.00%
发文量
97
审稿时长
>12 weeks
期刊介绍: Molecular Brain is an open access, peer-reviewed journal that considers manuscripts on all aspects of studies on the nervous system at the molecular, cellular, and systems level providing a forum for scientists to communicate their findings. Molecular brain research is a rapidly expanding research field in which integrative approaches at the genetic, molecular, cellular and synaptic levels yield key information about the physiological and pathological brain. These studies involve the use of a wide range of modern techniques in molecular biology, genomics, proteomics, imaging and electrophysiology.
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