Ultrasonic Neuromodulation via Astrocytic TRPA1

Authors
Oh, Soo-JinLee, Jung MooKim, Hyun-BumLee, JungpyoHan, SungminBae, Jin YoungHong, Gyu-SangKoh, WuhyunKwon, JeaHwang, Eun-SangWoo, Dong HoYoun, InchanCho, Il-JooBae, Yong ChulLee, SungonShim, Jae WanPark, Ji-HoLee, C. Justin
Issue Date
2019-10-21
Publisher
CELL PRESS
Citation
CURRENT BIOLOGY, v.29, no.20, pp.3386 - +
Abstract
Low-intensity, low-frequency ultrasound (LILFU) is the next-generation, non-invasive brain stimulation technology for treating various neurological and psychiatric disorders. However, the underlying cellular and molecular mechanism of LILFU-induced neuromodulation has remained unknown. Here, we report that LILFU-induced neuromodulation is initiated by opening of TRPA1 channels in astrocytes. The Ca2+ entry through TRPA1 causes a release of gliotransmitters including glutamate through Best1 channels in astrocytes. The released glutamate activates NMDA receptors in neighboring neurons to elicit action potential firing. Our results reveal an unprecedented mechanism of LILFU-induced neuromodulation, involving TRPA1 as a unique sensor for LILFU and glutamate-releasing Best1 as a mediator of glia-neuron interaction. These discoveries should prove to be useful for optimization of human brain stimulation and ultrasonogenetic manipulations of TRPA1.
Keywords
BRAIN-STIMULATION; CHANNEL; CONTRIBUTES; ANKYRIN; IDENTIFICATION; EXPRESSION; RESPONSES; CURRENTS; DYNAMICS; CAVEOLAE; BRAIN-STIMULATION; CHANNEL; CONTRIBUTES; ANKYRIN; IDENTIFICATION; EXPRESSION; RESPONSES; CURRENTS; DYNAMICS; CAVEOLAE; astrocyte; Best1; glutamate; neuromodulation; NMDAR; TRPA1; ultrasound
ISSN
0960-9822
URI
https://pubs.kist.re.kr/handle/201004/119434
DOI
10.1016/j.cub.2019.08.021
Appears in Collections:
KIST Article > 2019
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