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Mitochondrial Ca(2+) and membrane potential, an alternative pathway for Interleukin 6 to regulate CD4 cell effector function

IL-6 plays an important role in determining the fate of effector CD4 cells and the cytokines that these cells produce. Here we identify a novel molecular mechanism by which IL-6 regulates CD4 cell effector function. We show that IL-6-dependent signal facilitates the formation of mitochondrial respir...

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Autores principales: Yang, Rui, Lirussi, Dario, Thornton, Tina M, Jelley-Gibbs, Dawn M, Diehl, Sean A, Case, Laure K, Madesh, Muniswamy, Taatjes, Douglas J, Teuscher, Cory, Haynes, Laura, Rincón, Mercedes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4447996/
https://www.ncbi.nlm.nih.gov/pubmed/25974216
http://dx.doi.org/10.7554/eLife.06376
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author Yang, Rui
Lirussi, Dario
Thornton, Tina M
Jelley-Gibbs, Dawn M
Diehl, Sean A
Case, Laure K
Madesh, Muniswamy
Taatjes, Douglas J
Teuscher, Cory
Haynes, Laura
Rincón, Mercedes
author_facet Yang, Rui
Lirussi, Dario
Thornton, Tina M
Jelley-Gibbs, Dawn M
Diehl, Sean A
Case, Laure K
Madesh, Muniswamy
Taatjes, Douglas J
Teuscher, Cory
Haynes, Laura
Rincón, Mercedes
author_sort Yang, Rui
collection PubMed
description IL-6 plays an important role in determining the fate of effector CD4 cells and the cytokines that these cells produce. Here we identify a novel molecular mechanism by which IL-6 regulates CD4 cell effector function. We show that IL-6-dependent signal facilitates the formation of mitochondrial respiratory chain supercomplexes to sustain high mitochondrial membrane potential late during activation of CD4 cells. Mitochondrial hyperpolarization caused by IL-6 is uncoupled from the production of ATP by oxidative phosphorylation. However, it is a mechanism to raise the levels of mitochondrial Ca(2+) late during activation of CD4 cells. Increased levels of mitochondrial Ca(2+) in the presence of IL-6 are used to prolong Il4 and Il21 expression in effector CD4 cells. Thus, the effect of IL-6 on mitochondrial membrane potential and mitochondrial Ca(2+) is an alternative pathway by which IL-6 regulates effector function of CD4 cells and it could contribute to the pathogenesis of inflammatory diseases. DOI: http://dx.doi.org/10.7554/eLife.06376.001
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spelling pubmed-44479962015-05-29 Mitochondrial Ca(2+) and membrane potential, an alternative pathway for Interleukin 6 to regulate CD4 cell effector function Yang, Rui Lirussi, Dario Thornton, Tina M Jelley-Gibbs, Dawn M Diehl, Sean A Case, Laure K Madesh, Muniswamy Taatjes, Douglas J Teuscher, Cory Haynes, Laura Rincón, Mercedes eLife Immunology IL-6 plays an important role in determining the fate of effector CD4 cells and the cytokines that these cells produce. Here we identify a novel molecular mechanism by which IL-6 regulates CD4 cell effector function. We show that IL-6-dependent signal facilitates the formation of mitochondrial respiratory chain supercomplexes to sustain high mitochondrial membrane potential late during activation of CD4 cells. Mitochondrial hyperpolarization caused by IL-6 is uncoupled from the production of ATP by oxidative phosphorylation. However, it is a mechanism to raise the levels of mitochondrial Ca(2+) late during activation of CD4 cells. Increased levels of mitochondrial Ca(2+) in the presence of IL-6 are used to prolong Il4 and Il21 expression in effector CD4 cells. Thus, the effect of IL-6 on mitochondrial membrane potential and mitochondrial Ca(2+) is an alternative pathway by which IL-6 regulates effector function of CD4 cells and it could contribute to the pathogenesis of inflammatory diseases. DOI: http://dx.doi.org/10.7554/eLife.06376.001 eLife Sciences Publications, Ltd 2015-05-14 /pmc/articles/PMC4447996/ /pubmed/25974216 http://dx.doi.org/10.7554/eLife.06376 Text en http://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication (http://creativecommons.org/publicdomain/zero/1.0/) .
spellingShingle Immunology
Yang, Rui
Lirussi, Dario
Thornton, Tina M
Jelley-Gibbs, Dawn M
Diehl, Sean A
Case, Laure K
Madesh, Muniswamy
Taatjes, Douglas J
Teuscher, Cory
Haynes, Laura
Rincón, Mercedes
Mitochondrial Ca(2+) and membrane potential, an alternative pathway for Interleukin 6 to regulate CD4 cell effector function
title Mitochondrial Ca(2+) and membrane potential, an alternative pathway for Interleukin 6 to regulate CD4 cell effector function
title_full Mitochondrial Ca(2+) and membrane potential, an alternative pathway for Interleukin 6 to regulate CD4 cell effector function
title_fullStr Mitochondrial Ca(2+) and membrane potential, an alternative pathway for Interleukin 6 to regulate CD4 cell effector function
title_full_unstemmed Mitochondrial Ca(2+) and membrane potential, an alternative pathway for Interleukin 6 to regulate CD4 cell effector function
title_short Mitochondrial Ca(2+) and membrane potential, an alternative pathway for Interleukin 6 to regulate CD4 cell effector function
title_sort mitochondrial ca(2+) and membrane potential, an alternative pathway for interleukin 6 to regulate cd4 cell effector function
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4447996/
https://www.ncbi.nlm.nih.gov/pubmed/25974216
http://dx.doi.org/10.7554/eLife.06376
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