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Lipid Droplet Signaling in Metabolic Health and Aging

Lipid droplets (LDs) are neutral lipid rich organelles involved in lipid storage, fatty acid trafficking, and signaling. Emerging evidence from our laboratory and others suggests that the specific LD resident proteins couple/uncouple cells and tissues from inflammation and metabolic dysfunction. How...

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Autores principales: Najt, Charles, Mashek, Douglas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8679792/
http://dx.doi.org/10.1093/geroni/igab046.1761
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author Najt, Charles
Mashek, Douglas
author_facet Najt, Charles
Mashek, Douglas
author_sort Najt, Charles
collection PubMed
description Lipid droplets (LDs) are neutral lipid rich organelles involved in lipid storage, fatty acid trafficking, and signaling. Emerging evidence from our laboratory and others suggests that the specific LD resident proteins couple/uncouple cells and tissues from inflammation and metabolic dysfunction. However, the mechanism by which LD proteins influences these critical pathways remains unknown. We will present data delving into the role of LD proteins Perilipin (PLIN) 2 and 5 in balancing cellular energy metabolism, mitochondrial function, and inflammation. Data will be presented defining novel mechanisms through which PLIN2 orchestrates eicosanoid production as a means to promote inflammation. We will contrast these findings to PLIN5, which uncouples LD accumulation from metabolic dysfunction and inflammation, in part due to its promotion of SIRT1 signaling. Overall, these studies will highlight a crucial role of LD metabolism and signaling in regulating cellular energy homeostatic processes known to be key players in governing healthspan.
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spelling pubmed-86797922021-12-17 Lipid Droplet Signaling in Metabolic Health and Aging Najt, Charles Mashek, Douglas Innov Aging Abstracts Lipid droplets (LDs) are neutral lipid rich organelles involved in lipid storage, fatty acid trafficking, and signaling. Emerging evidence from our laboratory and others suggests that the specific LD resident proteins couple/uncouple cells and tissues from inflammation and metabolic dysfunction. However, the mechanism by which LD proteins influences these critical pathways remains unknown. We will present data delving into the role of LD proteins Perilipin (PLIN) 2 and 5 in balancing cellular energy metabolism, mitochondrial function, and inflammation. Data will be presented defining novel mechanisms through which PLIN2 orchestrates eicosanoid production as a means to promote inflammation. We will contrast these findings to PLIN5, which uncouples LD accumulation from metabolic dysfunction and inflammation, in part due to its promotion of SIRT1 signaling. Overall, these studies will highlight a crucial role of LD metabolism and signaling in regulating cellular energy homeostatic processes known to be key players in governing healthspan. Oxford University Press 2021-12-17 /pmc/articles/PMC8679792/ http://dx.doi.org/10.1093/geroni/igab046.1761 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of The Gerontological Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstracts
Najt, Charles
Mashek, Douglas
Lipid Droplet Signaling in Metabolic Health and Aging
title Lipid Droplet Signaling in Metabolic Health and Aging
title_full Lipid Droplet Signaling in Metabolic Health and Aging
title_fullStr Lipid Droplet Signaling in Metabolic Health and Aging
title_full_unstemmed Lipid Droplet Signaling in Metabolic Health and Aging
title_short Lipid Droplet Signaling in Metabolic Health and Aging
title_sort lipid droplet signaling in metabolic health and aging
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8679792/
http://dx.doi.org/10.1093/geroni/igab046.1761
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