Cargando…
Mitochondrial RNA stimulates beige adipocyte development in young mice
Childhood obesity is a serious public health crisis and a critical factor that determines future obesity prevalence. Signals affecting adipocyte development in early postnatal life have a strong potential to trigger childhood obesity; however, these signals are still poorly understood. We show here...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9771821/ https://www.ncbi.nlm.nih.gov/pubmed/36443525 http://dx.doi.org/10.1038/s42255-022-00683-w |
_version_ | 1784854898889719808 |
---|---|
author | Hoang, Anh Cuong Sasi-Szabó, László Pál, Tibor Szabó, Tamás Diedrich, Victoria Herwig, Annika Landgraf, Kathrin Körner, Antje Röszer, Tamás |
author_facet | Hoang, Anh Cuong Sasi-Szabó, László Pál, Tibor Szabó, Tamás Diedrich, Victoria Herwig, Annika Landgraf, Kathrin Körner, Antje Röszer, Tamás |
author_sort | Hoang, Anh Cuong |
collection | PubMed |
description | Childhood obesity is a serious public health crisis and a critical factor that determines future obesity prevalence. Signals affecting adipocyte development in early postnatal life have a strong potential to trigger childhood obesity; however, these signals are still poorly understood. We show here that mitochondrial (mt)RNA efflux stimulates transcription of nuclear-encoded genes for mitobiogenesis and thermogenesis in adipocytes of young mice and human infants. While cytosolic mtRNA is a potential trigger of the interferon (IFN) response, young adipocytes lack such a response to cytosolic mtRNA due to the suppression of IFN regulatory factor (IRF)7 expression by vitamin D receptor signalling. Adult and obese adipocytes, however, strongly express IRF7 and mount an IFN response to cytosolic mtRNA. In turn, suppressing IRF7 expression in adult adipocytes restores mtRNA-induced mitobiogenesis and thermogenesis and eventually mitigates obesity. Retrograde mitochondrion-to-nucleus signalling by mtRNA is thus a mechanism to evoke thermogenic potential during early adipocyte development and to protect against obesity. |
format | Online Article Text |
id | pubmed-9771821 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-97718212022-12-23 Mitochondrial RNA stimulates beige adipocyte development in young mice Hoang, Anh Cuong Sasi-Szabó, László Pál, Tibor Szabó, Tamás Diedrich, Victoria Herwig, Annika Landgraf, Kathrin Körner, Antje Röszer, Tamás Nat Metab Article Childhood obesity is a serious public health crisis and a critical factor that determines future obesity prevalence. Signals affecting adipocyte development in early postnatal life have a strong potential to trigger childhood obesity; however, these signals are still poorly understood. We show here that mitochondrial (mt)RNA efflux stimulates transcription of nuclear-encoded genes for mitobiogenesis and thermogenesis in adipocytes of young mice and human infants. While cytosolic mtRNA is a potential trigger of the interferon (IFN) response, young adipocytes lack such a response to cytosolic mtRNA due to the suppression of IFN regulatory factor (IRF)7 expression by vitamin D receptor signalling. Adult and obese adipocytes, however, strongly express IRF7 and mount an IFN response to cytosolic mtRNA. In turn, suppressing IRF7 expression in adult adipocytes restores mtRNA-induced mitobiogenesis and thermogenesis and eventually mitigates obesity. Retrograde mitochondrion-to-nucleus signalling by mtRNA is thus a mechanism to evoke thermogenic potential during early adipocyte development and to protect against obesity. Nature Publishing Group UK 2022-11-28 2022 /pmc/articles/PMC9771821/ /pubmed/36443525 http://dx.doi.org/10.1038/s42255-022-00683-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Hoang, Anh Cuong Sasi-Szabó, László Pál, Tibor Szabó, Tamás Diedrich, Victoria Herwig, Annika Landgraf, Kathrin Körner, Antje Röszer, Tamás Mitochondrial RNA stimulates beige adipocyte development in young mice |
title | Mitochondrial RNA stimulates beige adipocyte development in young mice |
title_full | Mitochondrial RNA stimulates beige adipocyte development in young mice |
title_fullStr | Mitochondrial RNA stimulates beige adipocyte development in young mice |
title_full_unstemmed | Mitochondrial RNA stimulates beige adipocyte development in young mice |
title_short | Mitochondrial RNA stimulates beige adipocyte development in young mice |
title_sort | mitochondrial rna stimulates beige adipocyte development in young mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9771821/ https://www.ncbi.nlm.nih.gov/pubmed/36443525 http://dx.doi.org/10.1038/s42255-022-00683-w |
work_keys_str_mv | AT hoanganhcuong mitochondrialrnastimulatesbeigeadipocytedevelopmentinyoungmice AT sasiszabolaszlo mitochondrialrnastimulatesbeigeadipocytedevelopmentinyoungmice AT paltibor mitochondrialrnastimulatesbeigeadipocytedevelopmentinyoungmice AT szabotamas mitochondrialrnastimulatesbeigeadipocytedevelopmentinyoungmice AT diedrichvictoria mitochondrialrnastimulatesbeigeadipocytedevelopmentinyoungmice AT herwigannika mitochondrialrnastimulatesbeigeadipocytedevelopmentinyoungmice AT landgrafkathrin mitochondrialrnastimulatesbeigeadipocytedevelopmentinyoungmice AT kornerantje mitochondrialrnastimulatesbeigeadipocytedevelopmentinyoungmice AT roszertamas mitochondrialrnastimulatesbeigeadipocytedevelopmentinyoungmice |