TMEM16A expression in cholinergic neurons of the medial habenula mediates anxiety-related behaviors

被引:24
作者
Cho, Chang-Hoon [1 ]
Lee, Sangjoon [2 ,3 ,4 ]
Kim, Ajung [5 ,6 ]
Yarishkin, Oleg [5 ]
Ryoo, Kanghyun [1 ]
Lee, Young-Sun [1 ]
Jung, Hyun-Gug [1 ,5 ]
Yang, Esther [7 ]
Lee, Da Yong [5 ]
Lee, Byeongjun [8 ]
Kim, Hyun [7 ]
Oh, Uhtaek [8 ]
Im, Heh-In [2 ,4 ,9 ]
Hwang, Eun Mi [5 ,6 ,9 ]
Park, Jae-Yong [1 ]
机构
[1] Korea Univ, Sch Biosyst & Biomed Sci, Coll Hlth Sci, Seoul, South Korea
[2] KIST, Convergence Res Ctr Diag Treatment & Care Syst De, Seoul, South Korea
[3] Seoul Natl Univ, Dept Pharmacol & Biomed Sci, Coll Med, Seoul, South Korea
[4] Korea Inst Sci & Technol, Brain Sci Inst, Ctr Neurosci, Seoul, South Korea
[5] KIST, Ctr Funct Connect, Seoul, South Korea
[6] Kyung Hee Univ, Grad Sch, KHU KIST Dept Converging Sci & Technol, Seoul, South Korea
[7] Korea Univ, Dept Anat, Coll Med, Seoul, South Korea
[8] Korea Inst Sci & Technol, Brain Sci Inst, Sensory Res Ctr, CRI, Seoul, South Korea
[9] Korea Univ Sci & Technol, KIST Sch, Div Biomed Sci & Technol, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
anxiety; cholinergic neurons; medial habenula; social interaction; TMEM16A; ACTIVATED CHLORIDE CHANNELS; ANOCTAMIN; NICOTINE WITHDRAWAL; SYNAPTIC RESPONSE; RECEPTORS; NUCLEUS; SEROTONIN; PATHWAY; MICE; TRANSMISSION;
D O I
10.15252/embr.201948097
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
TMEM16A, a Ca2+-activated Cl- channel, is known to modulate the excitability of various types of cells; however, its function in central neurons is largely unknown. Here, we show the specific expression of TMEM16A in the medial habenula (mHb) via RNAscope in situ hybridization, immunohistochemistry, and electrophysiology. When TMEM16A is ablated in the mHb cholinergic neurons (TMEM16A cKO mice), the slope of after-hyperpolarization of spontaneous action potentials decreases and the firing frequency is reduced. Reduced mHb activity also decreases the activity of the interpeduncular nucleus (IPN). Moreover, TMEM16A cKO mice display anxiogenic behaviors and deficits in social interaction without despair-like phenotypes or cognitive dysfunctions. Finally, chemogenetic inhibition of mHb cholinergic neurons using the DREADD (Designer Receptors Exclusively Activated by Designer Drugs) approach reveals similar behavioral phenotypes to those of TMEM16A cKO mice. We conclude that TMEM16A plays a key role in anxiety-related behaviors regulated by mHb cholinergic neurons and could be a potential therapeutic target against anxiety-related disorders.
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页数:15
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