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Gut-specific telomerase expression counteracts systemic aging in telomerase-deficient zebrafish
Telomere shortening is a hallmark of aging and is counteracted by telomerase. As in humans, the zebrafish gut is one of the organs with the fastest rate of telomere decline, triggering early tissue dysfunction during normal zebrafish aging and in prematurely aged telomerase mutants. However, whether...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group US
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10191862/ https://www.ncbi.nlm.nih.gov/pubmed/37142828 http://dx.doi.org/10.1038/s43587-023-00401-5 |
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author | El Maï, Mounir Bird, Malia Allouche, Asma Targen, Seniye Şerifoğlu, Naz Lopes-Bastos, Bruno Guigonis, Jean-Marie Kang, Da Pourcher, Thierry Yue, Jia-Xing Ferreira, Miguel Godinho |
author_facet | El Maï, Mounir Bird, Malia Allouche, Asma Targen, Seniye Şerifoğlu, Naz Lopes-Bastos, Bruno Guigonis, Jean-Marie Kang, Da Pourcher, Thierry Yue, Jia-Xing Ferreira, Miguel Godinho |
author_sort | El Maï, Mounir |
collection | PubMed |
description | Telomere shortening is a hallmark of aging and is counteracted by telomerase. As in humans, the zebrafish gut is one of the organs with the fastest rate of telomere decline, triggering early tissue dysfunction during normal zebrafish aging and in prematurely aged telomerase mutants. However, whether telomere-dependent aging of an individual organ, the gut, causes systemic aging is unknown. Here we show that tissue-specific telomerase expression in the gut can prevent telomere shortening and rescues premature aging of tert(−/−). Induction of telomerase rescues gut senescence and low cell proliferation, while restoring tissue integrity, inflammation and age-dependent microbiota dysbiosis. Averting gut aging causes systemic beneficial impacts, rescuing aging of distant organs such as reproductive and hematopoietic systems. Conclusively, we show that gut-specific telomerase expression extends the lifespan of tert(−/−) by 40%, while ameliorating natural aging. Our work demonstrates that gut-specific rescue of telomerase expression leading to telomere elongation is sufficient to systemically counteract aging in zebrafish. |
format | Online Article Text |
id | pubmed-10191862 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group US |
record_format | MEDLINE/PubMed |
spelling | pubmed-101918622023-05-19 Gut-specific telomerase expression counteracts systemic aging in telomerase-deficient zebrafish El Maï, Mounir Bird, Malia Allouche, Asma Targen, Seniye Şerifoğlu, Naz Lopes-Bastos, Bruno Guigonis, Jean-Marie Kang, Da Pourcher, Thierry Yue, Jia-Xing Ferreira, Miguel Godinho Nat Aging Article Telomere shortening is a hallmark of aging and is counteracted by telomerase. As in humans, the zebrafish gut is one of the organs with the fastest rate of telomere decline, triggering early tissue dysfunction during normal zebrafish aging and in prematurely aged telomerase mutants. However, whether telomere-dependent aging of an individual organ, the gut, causes systemic aging is unknown. Here we show that tissue-specific telomerase expression in the gut can prevent telomere shortening and rescues premature aging of tert(−/−). Induction of telomerase rescues gut senescence and low cell proliferation, while restoring tissue integrity, inflammation and age-dependent microbiota dysbiosis. Averting gut aging causes systemic beneficial impacts, rescuing aging of distant organs such as reproductive and hematopoietic systems. Conclusively, we show that gut-specific telomerase expression extends the lifespan of tert(−/−) by 40%, while ameliorating natural aging. Our work demonstrates that gut-specific rescue of telomerase expression leading to telomere elongation is sufficient to systemically counteract aging in zebrafish. Nature Publishing Group US 2023-05-04 2023 /pmc/articles/PMC10191862/ /pubmed/37142828 http://dx.doi.org/10.1038/s43587-023-00401-5 Text en © The Author(s) 2023 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 El Maï, Mounir Bird, Malia Allouche, Asma Targen, Seniye Şerifoğlu, Naz Lopes-Bastos, Bruno Guigonis, Jean-Marie Kang, Da Pourcher, Thierry Yue, Jia-Xing Ferreira, Miguel Godinho Gut-specific telomerase expression counteracts systemic aging in telomerase-deficient zebrafish |
title | Gut-specific telomerase expression counteracts systemic aging in telomerase-deficient zebrafish |
title_full | Gut-specific telomerase expression counteracts systemic aging in telomerase-deficient zebrafish |
title_fullStr | Gut-specific telomerase expression counteracts systemic aging in telomerase-deficient zebrafish |
title_full_unstemmed | Gut-specific telomerase expression counteracts systemic aging in telomerase-deficient zebrafish |
title_short | Gut-specific telomerase expression counteracts systemic aging in telomerase-deficient zebrafish |
title_sort | gut-specific telomerase expression counteracts systemic aging in telomerase-deficient zebrafish |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10191862/ https://www.ncbi.nlm.nih.gov/pubmed/37142828 http://dx.doi.org/10.1038/s43587-023-00401-5 |
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