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Controlling SIRT1 expression by microRNAs in health and metabolic disease
SIRT1 is a NAD(+-)dependent deacetylase implicated in longevity and diverse physiological processes. SIRT1, as a key mediator of beneficial effects of caloric restriction, regulates lipid and glucose metabolism by deacetylating metabolic regulators, as well as histones, in response to nutritional de...
Autores principales: | , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2954045/ https://www.ncbi.nlm.nih.gov/pubmed/20689156 |
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author | Lee, Jiyoung Kemper, Jongsook Kim |
author_facet | Lee, Jiyoung Kemper, Jongsook Kim |
author_sort | Lee, Jiyoung |
collection | PubMed |
description | SIRT1 is a NAD(+-)dependent deacetylase implicated in longevity and diverse physiological processes. SIRT1, as a key mediator of beneficial effects of caloric restriction, regulates lipid and glucose metabolism by deacetylating metabolic regulators, as well as histones, in response to nutritional deprivation. Here we discuss how SIRT1 levels are regulated by microRNAs (miRs) which are emerging as important metabolic regulators; the recently identified nuclear receptor FXR/SHP cascade pathway that controls the expression of miR-34a and its target SIRT1; and a FXR/SIRT1 positive feedback regulatory loop, which is deregulated in metabolic disease states. The FXR/miR-34a pathway and other miRs controlling SIRT1 may be useful therapeutic targets for age-related diseases, including metabolic disorders. |
format | Text |
id | pubmed-2954045 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-29540452010-10-14 Controlling SIRT1 expression by microRNAs in health and metabolic disease Lee, Jiyoung Kemper, Jongsook Kim Aging (Albany NY) Research Perspective SIRT1 is a NAD(+-)dependent deacetylase implicated in longevity and diverse physiological processes. SIRT1, as a key mediator of beneficial effects of caloric restriction, regulates lipid and glucose metabolism by deacetylating metabolic regulators, as well as histones, in response to nutritional deprivation. Here we discuss how SIRT1 levels are regulated by microRNAs (miRs) which are emerging as important metabolic regulators; the recently identified nuclear receptor FXR/SHP cascade pathway that controls the expression of miR-34a and its target SIRT1; and a FXR/SIRT1 positive feedback regulatory loop, which is deregulated in metabolic disease states. The FXR/miR-34a pathway and other miRs controlling SIRT1 may be useful therapeutic targets for age-related diseases, including metabolic disorders. Impact Journals LLC 2010-08-05 /pmc/articles/PMC2954045/ /pubmed/20689156 Text en Copyright: ©2010 Lee et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Perspective Lee, Jiyoung Kemper, Jongsook Kim Controlling SIRT1 expression by microRNAs in health and metabolic disease |
title | Controlling SIRT1 expression by microRNAs in health and metabolic disease |
title_full | Controlling SIRT1 expression by microRNAs in health and metabolic disease |
title_fullStr | Controlling SIRT1 expression by microRNAs in health and metabolic disease |
title_full_unstemmed | Controlling SIRT1 expression by microRNAs in health and metabolic disease |
title_short | Controlling SIRT1 expression by microRNAs in health and metabolic disease |
title_sort | controlling sirt1 expression by micrornas in health and metabolic disease |
topic | Research Perspective |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2954045/ https://www.ncbi.nlm.nih.gov/pubmed/20689156 |
work_keys_str_mv | AT leejiyoung controllingsirt1expressionbymicrornasinhealthandmetabolicdisease AT kemperjongsookkim controllingsirt1expressionbymicrornasinhealthandmetabolicdisease |