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FASN activity is important for the initial stages of the induction of senescence

Senescent cells accumulate in several tissues during ageing and contribute to several pathological processes such as ageing and cancer. Senescence induction is a complex process not well defined yet and is characterized by a series of molecular changes acquired after an initial growth arrest. We fou...

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Autores principales: Fafián-Labora, Juan, Carpintero-Fernández, Paula, Jordan, Samuel James Davison, Shikh-Bahaei, Tamanna, Abdullah, Sana Mohammad, Mahenthiran, Midusa, Rodríguez-Navarro, José Antonio, Niklison-Chirou, Maria Victoria, O’Loghlen, Ana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6453932/
https://www.ncbi.nlm.nih.gov/pubmed/30962418
http://dx.doi.org/10.1038/s41419-019-1550-0
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author Fafián-Labora, Juan
Carpintero-Fernández, Paula
Jordan, Samuel James Davison
Shikh-Bahaei, Tamanna
Abdullah, Sana Mohammad
Mahenthiran, Midusa
Rodríguez-Navarro, José Antonio
Niklison-Chirou, Maria Victoria
O’Loghlen, Ana
author_facet Fafián-Labora, Juan
Carpintero-Fernández, Paula
Jordan, Samuel James Davison
Shikh-Bahaei, Tamanna
Abdullah, Sana Mohammad
Mahenthiran, Midusa
Rodríguez-Navarro, José Antonio
Niklison-Chirou, Maria Victoria
O’Loghlen, Ana
author_sort Fafián-Labora, Juan
collection PubMed
description Senescent cells accumulate in several tissues during ageing and contribute to several pathological processes such as ageing and cancer. Senescence induction is a complex process not well defined yet and is characterized by a series of molecular changes acquired after an initial growth arrest. We found that fatty acid synthase (FASN) levels increase during the induction of senescence in mouse hepatic stellate cells and human primary fibroblasts. Importantly, we also observed a significant increase in FASN levels during ageing in mouse liver tissues. To probe the central role of FASN in senescence induction, we used a small-molecule inhibitor of FASN activity, C75. We found that C75 treatment prevented the induction of senescence in mouse and human senescent cells. Importantly, C75 also reduced the expression of the signature SASP factors interleukin 1α (IL-1α), IL-1β and IL-6, and suppressed the secretion of small extracellular vesicles. These findings were confirmed using a shRNA targeting FASN. In addition, we find that FASN inhibition induces metabolic changes in senescent cells. Our work underscores the importance of C75 as a pharmacological inhibitor for reducing the impact of senescent cell accumulation.
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spelling pubmed-64539322019-04-09 FASN activity is important for the initial stages of the induction of senescence Fafián-Labora, Juan Carpintero-Fernández, Paula Jordan, Samuel James Davison Shikh-Bahaei, Tamanna Abdullah, Sana Mohammad Mahenthiran, Midusa Rodríguez-Navarro, José Antonio Niklison-Chirou, Maria Victoria O’Loghlen, Ana Cell Death Dis Article Senescent cells accumulate in several tissues during ageing and contribute to several pathological processes such as ageing and cancer. Senescence induction is a complex process not well defined yet and is characterized by a series of molecular changes acquired after an initial growth arrest. We found that fatty acid synthase (FASN) levels increase during the induction of senescence in mouse hepatic stellate cells and human primary fibroblasts. Importantly, we also observed a significant increase in FASN levels during ageing in mouse liver tissues. To probe the central role of FASN in senescence induction, we used a small-molecule inhibitor of FASN activity, C75. We found that C75 treatment prevented the induction of senescence in mouse and human senescent cells. Importantly, C75 also reduced the expression of the signature SASP factors interleukin 1α (IL-1α), IL-1β and IL-6, and suppressed the secretion of small extracellular vesicles. These findings were confirmed using a shRNA targeting FASN. In addition, we find that FASN inhibition induces metabolic changes in senescent cells. Our work underscores the importance of C75 as a pharmacological inhibitor for reducing the impact of senescent cell accumulation. Nature Publishing Group UK 2019-04-08 /pmc/articles/PMC6453932/ /pubmed/30962418 http://dx.doi.org/10.1038/s41419-019-1550-0 Text en © The Author(s) 2019 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
Fafián-Labora, Juan
Carpintero-Fernández, Paula
Jordan, Samuel James Davison
Shikh-Bahaei, Tamanna
Abdullah, Sana Mohammad
Mahenthiran, Midusa
Rodríguez-Navarro, José Antonio
Niklison-Chirou, Maria Victoria
O’Loghlen, Ana
FASN activity is important for the initial stages of the induction of senescence
title FASN activity is important for the initial stages of the induction of senescence
title_full FASN activity is important for the initial stages of the induction of senescence
title_fullStr FASN activity is important for the initial stages of the induction of senescence
title_full_unstemmed FASN activity is important for the initial stages of the induction of senescence
title_short FASN activity is important for the initial stages of the induction of senescence
title_sort fasn activity is important for the initial stages of the induction of senescence
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6453932/
https://www.ncbi.nlm.nih.gov/pubmed/30962418
http://dx.doi.org/10.1038/s41419-019-1550-0
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