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Mitochondrial function provides instructive signals for activation-induced B-cell fates
During immune reactions, functionally distinct B-cell subsets are generated by stochastic processes, including class-switch recombination (CSR) and plasma cell differentiation (PCD). In this study, we show a strong association between individual B-cell fates and mitochondrial functions. CSR occurs s...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Pub. Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4403446/ https://www.ncbi.nlm.nih.gov/pubmed/25857523 http://dx.doi.org/10.1038/ncomms7750 |
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author | Jang, Kyoung-Jin Mano, Hiroto Aoki, Koji Hayashi, Tatsunari Muto, Akihiko Nambu, Yukiko Takahashi, Katsu Itoh, Katsuhiko Taketani, Shigeru Nutt, Stephen L. Igarashi, Kazuhiko Shimizu, Akira Sugai, Manabu |
author_facet | Jang, Kyoung-Jin Mano, Hiroto Aoki, Koji Hayashi, Tatsunari Muto, Akihiko Nambu, Yukiko Takahashi, Katsu Itoh, Katsuhiko Taketani, Shigeru Nutt, Stephen L. Igarashi, Kazuhiko Shimizu, Akira Sugai, Manabu |
author_sort | Jang, Kyoung-Jin |
collection | PubMed |
description | During immune reactions, functionally distinct B-cell subsets are generated by stochastic processes, including class-switch recombination (CSR) and plasma cell differentiation (PCD). In this study, we show a strong association between individual B-cell fates and mitochondrial functions. CSR occurs specifically in activated B cells with increased mitochondrial mass and membrane potential, which augment mitochondrial reactive oxygen species (mROS), whereas PCD occurs in cells with decreased mitochondrial mass and potential. These events are consequences of initial slight changes in mROS in mitochondria(high) B-cell populations. In CSR-committed cells, mROS attenuates haeme synthesis by inhibiting ferrous ion addition to protoporphyrin IX, thereby maintaining Bach2 function. Reduced mROS then promotes PCD by increasing haeme synthesis. In PCD-committed cells, Blimp1 reduces mitochondrial mass, thereby reducing mROS levels. Identifying mROS as a haeme synthesis regulator increases the understanding of mechanisms regulating haeme homeostasis and cell fate determination after B-cell activation. |
format | Online Article Text |
id | pubmed-4403446 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Pub. Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-44034462015-04-29 Mitochondrial function provides instructive signals for activation-induced B-cell fates Jang, Kyoung-Jin Mano, Hiroto Aoki, Koji Hayashi, Tatsunari Muto, Akihiko Nambu, Yukiko Takahashi, Katsu Itoh, Katsuhiko Taketani, Shigeru Nutt, Stephen L. Igarashi, Kazuhiko Shimizu, Akira Sugai, Manabu Nat Commun Article During immune reactions, functionally distinct B-cell subsets are generated by stochastic processes, including class-switch recombination (CSR) and plasma cell differentiation (PCD). In this study, we show a strong association between individual B-cell fates and mitochondrial functions. CSR occurs specifically in activated B cells with increased mitochondrial mass and membrane potential, which augment mitochondrial reactive oxygen species (mROS), whereas PCD occurs in cells with decreased mitochondrial mass and potential. These events are consequences of initial slight changes in mROS in mitochondria(high) B-cell populations. In CSR-committed cells, mROS attenuates haeme synthesis by inhibiting ferrous ion addition to protoporphyrin IX, thereby maintaining Bach2 function. Reduced mROS then promotes PCD by increasing haeme synthesis. In PCD-committed cells, Blimp1 reduces mitochondrial mass, thereby reducing mROS levels. Identifying mROS as a haeme synthesis regulator increases the understanding of mechanisms regulating haeme homeostasis and cell fate determination after B-cell activation. Nature Pub. Group 2015-04-10 /pmc/articles/PMC4403446/ /pubmed/25857523 http://dx.doi.org/10.1038/ncomms7750 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Jang, Kyoung-Jin Mano, Hiroto Aoki, Koji Hayashi, Tatsunari Muto, Akihiko Nambu, Yukiko Takahashi, Katsu Itoh, Katsuhiko Taketani, Shigeru Nutt, Stephen L. Igarashi, Kazuhiko Shimizu, Akira Sugai, Manabu Mitochondrial function provides instructive signals for activation-induced B-cell fates |
title | Mitochondrial function provides instructive signals for activation-induced B-cell fates |
title_full | Mitochondrial function provides instructive signals for activation-induced B-cell fates |
title_fullStr | Mitochondrial function provides instructive signals for activation-induced B-cell fates |
title_full_unstemmed | Mitochondrial function provides instructive signals for activation-induced B-cell fates |
title_short | Mitochondrial function provides instructive signals for activation-induced B-cell fates |
title_sort | mitochondrial function provides instructive signals for activation-induced b-cell fates |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4403446/ https://www.ncbi.nlm.nih.gov/pubmed/25857523 http://dx.doi.org/10.1038/ncomms7750 |
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