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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2020
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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. |
format | Online Article Text |
id | pubmed-7703602 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
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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