乙酰胆碱
胆碱能的
迷走神经
迷走神经电刺激
烟碱乙酰胆碱受体
神经科学
乙酰胆碱受体
生物
内科学
刺激
内分泌学
医学
受体
作者
Mauricio Rosas‐Ballina,Peder S. Olofsson,Mahendar Ochani,Sergio Iván Valdés‐Ferrer,Yaakov A. Levine,Colin Reardon,Michael W. Tusche,Valentin A. Pavlov,Jan Andersson,Sangeeta S. Chavan,Tak W. Mak,Kevin J. Tracey
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2011-09-16
卷期号:334 (6052): 98-101
被引量:1333
标识
DOI:10.1126/science.1209985
摘要
Neural circuits regulate cytokine production to prevent potentially damaging inflammation. A prototypical vagus nerve circuit, the inflammatory reflex, inhibits tumor necrosis factor-α production in spleen by a mechanism requiring acetylcholine signaling through the α7 nicotinic acetylcholine receptor expressed on cytokine-producing macrophages. Nerve fibers in spleen lack the enzymatic machinery necessary for acetylcholine production; therefore, how does this neural circuit terminate in cholinergic signaling? We identified an acetylcholine-producing, memory phenotype T cell population in mice that is integral to the inflammatory reflex. These acetylcholine-producing T cells are required for inhibition of cytokine production by vagus nerve stimulation. Thus, action potentials originating in the vagus nerve regulate T cells, which in turn produce the neurotransmitter, acetylcholine, required to control innate immune responses.
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