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MAVS is energized by Mff which senses mitochondrial metabolism via AMPK for acute antiviral immunity

Mitochondria are multifunctional organelles that produce energy and are critical for various signaling pathways. Mitochondrial antiviral signaling (MAVS) is a mitochondrial outer membrane protein essential for the anti-RNA viral immune response, which is regulated by mitochondrial dynamics and energ...

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Autores principales: Hanada, Yuki, Ishihara, Naotada, Wang, Lixiang, Otera, Hidenori, Ishihara, Takaya, Koshiba, Takumi, Mihara, Katsuyoshi, Ogawa, Yoshihiro, Nomura, Masatoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7658986/
https://www.ncbi.nlm.nih.gov/pubmed/33177519
http://dx.doi.org/10.1038/s41467-020-19287-7
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author Hanada, Yuki
Ishihara, Naotada
Wang, Lixiang
Otera, Hidenori
Ishihara, Takaya
Koshiba, Takumi
Mihara, Katsuyoshi
Ogawa, Yoshihiro
Nomura, Masatoshi
author_facet Hanada, Yuki
Ishihara, Naotada
Wang, Lixiang
Otera, Hidenori
Ishihara, Takaya
Koshiba, Takumi
Mihara, Katsuyoshi
Ogawa, Yoshihiro
Nomura, Masatoshi
author_sort Hanada, Yuki
collection PubMed
description Mitochondria are multifunctional organelles that produce energy and are critical for various signaling pathways. Mitochondrial antiviral signaling (MAVS) is a mitochondrial outer membrane protein essential for the anti-RNA viral immune response, which is regulated by mitochondrial dynamics and energetics; however, the molecular link between mitochondrial metabolism and immunity is unclear. Here we show in cultured mammalian cells that MAVS is activated by mitochondrial fission factor (Mff), which senses mitochondrial energy status. Mff mediates the formation of active MAVS clusters on mitochondria, independent of mitochondrial fission and dynamin-related protein 1. Under mitochondrial dysfunction, Mff is phosphorylated by the cellular energy sensor AMP-activated protein kinase (AMPK), leading to the disorganization of MAVS clusters and repression of the acute antiviral response. Mff also contributes to immune tolerance during chronic infection by disrupting the mitochondrial MAVS clusters. Taken together, Mff has a critical function in MAVS-mediated innate immunity, by sensing mitochondrial energy metabolism via AMPK signaling.
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spelling pubmed-76589862020-11-17 MAVS is energized by Mff which senses mitochondrial metabolism via AMPK for acute antiviral immunity Hanada, Yuki Ishihara, Naotada Wang, Lixiang Otera, Hidenori Ishihara, Takaya Koshiba, Takumi Mihara, Katsuyoshi Ogawa, Yoshihiro Nomura, Masatoshi Nat Commun Article Mitochondria are multifunctional organelles that produce energy and are critical for various signaling pathways. Mitochondrial antiviral signaling (MAVS) is a mitochondrial outer membrane protein essential for the anti-RNA viral immune response, which is regulated by mitochondrial dynamics and energetics; however, the molecular link between mitochondrial metabolism and immunity is unclear. Here we show in cultured mammalian cells that MAVS is activated by mitochondrial fission factor (Mff), which senses mitochondrial energy status. Mff mediates the formation of active MAVS clusters on mitochondria, independent of mitochondrial fission and dynamin-related protein 1. Under mitochondrial dysfunction, Mff is phosphorylated by the cellular energy sensor AMP-activated protein kinase (AMPK), leading to the disorganization of MAVS clusters and repression of the acute antiviral response. Mff also contributes to immune tolerance during chronic infection by disrupting the mitochondrial MAVS clusters. Taken together, Mff has a critical function in MAVS-mediated innate immunity, by sensing mitochondrial energy metabolism via AMPK signaling. Nature Publishing Group UK 2020-11-11 /pmc/articles/PMC7658986/ /pubmed/33177519 http://dx.doi.org/10.1038/s41467-020-19287-7 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Hanada, Yuki
Ishihara, Naotada
Wang, Lixiang
Otera, Hidenori
Ishihara, Takaya
Koshiba, Takumi
Mihara, Katsuyoshi
Ogawa, Yoshihiro
Nomura, Masatoshi
MAVS is energized by Mff which senses mitochondrial metabolism via AMPK for acute antiviral immunity
title MAVS is energized by Mff which senses mitochondrial metabolism via AMPK for acute antiviral immunity
title_full MAVS is energized by Mff which senses mitochondrial metabolism via AMPK for acute antiviral immunity
title_fullStr MAVS is energized by Mff which senses mitochondrial metabolism via AMPK for acute antiviral immunity
title_full_unstemmed MAVS is energized by Mff which senses mitochondrial metabolism via AMPK for acute antiviral immunity
title_short MAVS is energized by Mff which senses mitochondrial metabolism via AMPK for acute antiviral immunity
title_sort mavs is energized by mff which senses mitochondrial metabolism via ampk for acute antiviral immunity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7658986/
https://www.ncbi.nlm.nih.gov/pubmed/33177519
http://dx.doi.org/10.1038/s41467-020-19287-7
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