| Literature DB >> 31782602 |
Chang-Hoon Cho1, Sangjoon Lee2,3,4, Ajung Kim5,6, Oleg Yarishkin5, Kanghyun Ryoo1, Young-Sun Lee1, Hyun-Gug Jung1,5, Esther Yang7, Da Yong Lee5, Byeongjun Lee8, Hyun Kim7, Uhtaek Oh8, Heh-In Im2,4,9, Eun Mi Hwang5,6,9, Jae-Yong Park1.
Abstract
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.Entities:
Keywords: TMEM16A; anxiety; cholinergic neurons; medial habenula; social interaction
Mesh:
Year: 2019 PMID: 31782602 PMCID: PMC7001509 DOI: 10.15252/embr.201948097
Source DB: PubMed Journal: EMBO Rep ISSN: 1469-221X Impact factor: 8.807