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

Authors
Cho, Chang-HoonLee, SangjoonKim, AjungYarishkin, OlegRyoo, KanghyunLee, Young-SunJung, Hyun-GugYang, EstherLee, Da YongLee, ByeongjunKim, HyunOh, UhtaekIm, Heh-InHwang, Eun MiPark, Jae-Yong
Issue Date
2020-02
Publisher
Nature Publishing Group
Citation
EMBO Reports, v.21, no.2
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.
Keywords
ACTIVATED CHLORIDE CHANNELS; ANOCTAMIN 1; NICOTINE WITHDRAWAL; SYNAPTIC RESPONSE; RECEPTORS; NUCLEUS; SEROTONIN; PATHWAY; MICE; TRANSMISSION; anxiety; cholinergic neurons; medial habenula; social interaction; TMEM16A
ISSN
1469-221X
URI
https://pubs.kist.re.kr/handle/201004/119039
DOI
10.15252/embr.201948097
Appears in Collections:
KIST Article > 2020
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