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Identification of a brainstem locus that inhibits tumor necrosis factor

In the brain, compact clusters of neuron cell bodies, termed nuclei, are essential for maintaining parameters of host physiology within a narrow range optimal for health. Neurons residing in the brainstem dorsal motor nucleus (DMN) project in the vagus nerve to communicate with the lungs, liver, gas...

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Autores principales: Kressel, Adam M., Tsaava, Tea, Levine, Yaakov A., Chang, Eric H., Addorisio, Meghan E., Chang, Qing, Burbach, Barry J., Carnevale, Daniela, Lembo, Giuseppe, Zador, Anthony M., Andersson, Ulf, Pavlov, Valentin A., Chavan, Sangeeta S., Tracey, Kevin J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7703602/
https://www.ncbi.nlm.nih.gov/pubmed/33168718
http://dx.doi.org/10.1073/pnas.2008213117
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author Kressel, Adam M.
Tsaava, Tea
Levine, Yaakov A.
Chang, Eric H.
Addorisio, Meghan E.
Chang, Qing
Burbach, Barry J.
Carnevale, Daniela
Lembo, Giuseppe
Zador, Anthony M.
Andersson, Ulf
Pavlov, Valentin A.
Chavan, Sangeeta S.
Tracey, Kevin J.
author_facet Kressel, Adam M.
Tsaava, Tea
Levine, Yaakov A.
Chang, Eric H.
Addorisio, Meghan E.
Chang, Qing
Burbach, Barry J.
Carnevale, Daniela
Lembo, Giuseppe
Zador, Anthony M.
Andersson, Ulf
Pavlov, Valentin A.
Chavan, Sangeeta S.
Tracey, Kevin J.
author_sort Kressel, Adam M.
collection PubMed
description In the brain, compact clusters of neuron cell bodies, termed nuclei, are essential for maintaining parameters of host physiology within a narrow range optimal for health. Neurons residing in the brainstem dorsal motor nucleus (DMN) project in the vagus nerve to communicate with the lungs, liver, gastrointestinal tract, and other organs. Vagus nerve-mediated reflexes also control immune system responses to infection and injury by inhibiting the production of tumor necrosis factor (TNF) and other cytokines in the spleen, although the function of DMN neurons in regulating TNF release is not known. Here, optogenetics and functional mapping reveal cholinergic neurons in the DMN, which project to the celiac-superior mesenteric ganglia, significantly increase splenic nerve activity and inhibit TNF production. Efferent vagus nerve fibers terminating in the celiac-superior mesenteric ganglia form varicose-like structures surrounding individual nerve cell bodies innervating the spleen. Selective optogenetic activation of DMN cholinergic neurons or electrical activation of the cervical vagus nerve evokes action potentials in the splenic nerve. Pharmacological blockade and surgical transection of the vagus nerve inhibit vagus nerve-evoked splenic nerve responses. These results indicate that cholinergic neurons residing in the brainstem DMN control TNF production, revealing a role for brainstem coordination of immunity.
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spelling pubmed-77036022020-12-10 Identification of a brainstem locus that inhibits tumor necrosis factor Kressel, Adam M. Tsaava, Tea Levine, Yaakov A. Chang, Eric H. Addorisio, Meghan E. Chang, Qing Burbach, Barry J. Carnevale, Daniela Lembo, Giuseppe Zador, Anthony M. Andersson, Ulf Pavlov, Valentin A. Chavan, Sangeeta S. Tracey, Kevin J. Proc Natl Acad Sci U S A Biological Sciences In the brain, compact clusters of neuron cell bodies, termed nuclei, are essential for maintaining parameters of host physiology within a narrow range optimal for health. Neurons residing in the brainstem dorsal motor nucleus (DMN) project in the vagus nerve to communicate with the lungs, liver, gastrointestinal tract, and other organs. Vagus nerve-mediated reflexes also control immune system responses to infection and injury by inhibiting the production of tumor necrosis factor (TNF) and other cytokines in the spleen, although the function of DMN neurons in regulating TNF release is not known. Here, optogenetics and functional mapping reveal cholinergic neurons in the DMN, which project to the celiac-superior mesenteric ganglia, significantly increase splenic nerve activity and inhibit TNF production. Efferent vagus nerve fibers terminating in the celiac-superior mesenteric ganglia form varicose-like structures surrounding individual nerve cell bodies innervating the spleen. Selective optogenetic activation of DMN cholinergic neurons or electrical activation of the cervical vagus nerve evokes action potentials in the splenic nerve. Pharmacological blockade and surgical transection of the vagus nerve inhibit vagus nerve-evoked splenic nerve responses. These results indicate that cholinergic neurons residing in the brainstem DMN control TNF production, revealing a role for brainstem coordination of immunity. National Academy of Sciences 2020-11-24 2020-11-09 /pmc/articles/PMC7703602/ /pubmed/33168718 http://dx.doi.org/10.1073/pnas.2008213117 Text en Copyright © 2020 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Kressel, Adam M.
Tsaava, Tea
Levine, Yaakov A.
Chang, Eric H.
Addorisio, Meghan E.
Chang, Qing
Burbach, Barry J.
Carnevale, Daniela
Lembo, Giuseppe
Zador, Anthony M.
Andersson, Ulf
Pavlov, Valentin A.
Chavan, Sangeeta S.
Tracey, Kevin J.
Identification of a brainstem locus that inhibits tumor necrosis factor
title Identification of a brainstem locus that inhibits tumor necrosis factor
title_full Identification of a brainstem locus that inhibits tumor necrosis factor
title_fullStr Identification of a brainstem locus that inhibits tumor necrosis factor
title_full_unstemmed Identification of a brainstem locus that inhibits tumor necrosis factor
title_short Identification of a brainstem locus that inhibits tumor necrosis factor
title_sort identification of a brainstem locus that inhibits tumor necrosis factor
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7703602/
https://www.ncbi.nlm.nih.gov/pubmed/33168718
http://dx.doi.org/10.1073/pnas.2008213117
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