海马体
海马结构
加巴能
抑制性突触后电位
颞叶
神经元
神经科学
生物
癫痫
作者
Wei Jing,Tongmei Zhang,Jiaying Liu,Xian Huang,Quntao Yu,Hongyan Yu,Qingping Zhang,Hao Li,Man‐Fei Deng,Ling‐Qiang Zhu,Huiyun Du,Youming Lu
出处
期刊:Cell Reports
[Cell Press]
日期:2021-12-01
卷期号:37 (13): 110177-110177
被引量:18
标识
DOI:10.1016/j.celrep.2021.110177
摘要
The hippocampus is a temporal lobe structure critical for cognition, such as learning, memory, and attention, as well as emotional responses. Hippocampal dysfunction can lead to persistent anxiety and/or depression. However, how millions of neurons in the hippocampus are molecularly and structurally organized to engage their divergent functions remains unknown. Here, we genetically target a subset of neurons expressing the coagulation factor c homolog (COCH) gene. COCH-expressing neurons or COCH neurons are topographically segregated in the distal region of the ventral CA3 hippocampus and express Mtf1 and Cacna1h. MTF1 activation of Cacna1h transcription in COCH neurons encodes the ability of COCH neurons to burst action potentials and cause social-stress-induced anxiety-like behaviors by synapsing directly with a subset of GABAergic inhibitory neurons in the lateral septum. Together, this study provides a molecular and circuitry-based framework for understanding how COCH neurons in the hippocampus are assembled to engage social behavior.
科研通智能强力驱动
Strongly Powered by AbleSci AI