Acetylcholine-Synthesizing T Cells Relay Neural Signals in a Vagus Nerve Circuit

Mauricio Rosas‐Ballina(Feinstein Institute for Medical Research), Peder S. Olofsson(Feinstein Institute for Medical Research), Mahendar Ochani(Feinstein Institute for Medical Research), Sergio Iván Valdés‐Ferrer(Feinstein Institute for Medical Research), Yaakov A. Levine(Feinstein Institute for Medical Research), Colin Reardon(Ontario Institute for Cancer Research), Michael W. Tusche(Ontario Institute for Cancer Research), Valentin A. Pavlov(Feinstein Institute for Medical Research), Ulf Andersson(Karolinska Institutet), Sangeeta S. Chavan(Feinstein Institute for Medical Research), Tak W. Mak(Ontario Institute for Cancer Research), Kevin J. Tracey(Feinstein Institute for Medical Research)
Science
September 16, 2011
Cited by 1,526Open Access
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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.


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