| Literature DB >> 21921156 |
Mauricio Rosas-Ballina1, Peder S Olofsson, Mahendar Ochani, Sergio I Valdés-Ferrer, Yaakov A Levine, Colin Reardon, Michael W Tusche, Valentin A Pavlov, Ulf Andersson, Sangeeta Chavan, Tak W Mak, Kevin J Tracey.
Abstract
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.Entities:
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Year: 2011 PMID: 21921156 PMCID: PMC4548937 DOI: 10.1126/science.1209985
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728