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Modulation of Obesity and Insulin Resistance by the Redox Enzyme and Adaptor Protein p66(Shc)
Initially reported as a longevity-related protein, the 66 kDa isoform of the mammalian Shc1 locus has been implicated in several metabolic pathways, being able to act both as an adaptor protein and as a redox enzyme capable of generating reactive oxygen species (ROS) when it localizes to the mitocho...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6412263/ https://www.ncbi.nlm.nih.gov/pubmed/30813483 http://dx.doi.org/10.3390/ijms20040985 |
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author | Ciciliot, Stefano Fadini, Gian Paolo |
author_facet | Ciciliot, Stefano Fadini, Gian Paolo |
author_sort | Ciciliot, Stefano |
collection | PubMed |
description | Initially reported as a longevity-related protein, the 66 kDa isoform of the mammalian Shc1 locus has been implicated in several metabolic pathways, being able to act both as an adaptor protein and as a redox enzyme capable of generating reactive oxygen species (ROS) when it localizes to the mitochondrion. Ablation of p66(Shc) has been shown to be protective against obesity and the insurgence of insulin resistance, but not all the studies available in the literature agree on these points. This review will focus in particular on the role of p66(Shc) in the modulation of glucose homeostasis, obesity, body temperature, and respiration/energy expenditure. In view of the obesity and diabetes epidemic, p66(Shc) may represent a promising therapeutic target with enormous implications for human health. |
format | Online Article Text |
id | pubmed-6412263 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64122632019-04-05 Modulation of Obesity and Insulin Resistance by the Redox Enzyme and Adaptor Protein p66(Shc) Ciciliot, Stefano Fadini, Gian Paolo Int J Mol Sci Review Initially reported as a longevity-related protein, the 66 kDa isoform of the mammalian Shc1 locus has been implicated in several metabolic pathways, being able to act both as an adaptor protein and as a redox enzyme capable of generating reactive oxygen species (ROS) when it localizes to the mitochondrion. Ablation of p66(Shc) has been shown to be protective against obesity and the insurgence of insulin resistance, but not all the studies available in the literature agree on these points. This review will focus in particular on the role of p66(Shc) in the modulation of glucose homeostasis, obesity, body temperature, and respiration/energy expenditure. In view of the obesity and diabetes epidemic, p66(Shc) may represent a promising therapeutic target with enormous implications for human health. MDPI 2019-02-24 /pmc/articles/PMC6412263/ /pubmed/30813483 http://dx.doi.org/10.3390/ijms20040985 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Ciciliot, Stefano Fadini, Gian Paolo Modulation of Obesity and Insulin Resistance by the Redox Enzyme and Adaptor Protein p66(Shc) |
title | Modulation of Obesity and Insulin Resistance by the Redox Enzyme and Adaptor Protein p66(Shc) |
title_full | Modulation of Obesity and Insulin Resistance by the Redox Enzyme and Adaptor Protein p66(Shc) |
title_fullStr | Modulation of Obesity and Insulin Resistance by the Redox Enzyme and Adaptor Protein p66(Shc) |
title_full_unstemmed | Modulation of Obesity and Insulin Resistance by the Redox Enzyme and Adaptor Protein p66(Shc) |
title_short | Modulation of Obesity and Insulin Resistance by the Redox Enzyme and Adaptor Protein p66(Shc) |
title_sort | modulation of obesity and insulin resistance by the redox enzyme and adaptor protein p66(shc) |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6412263/ https://www.ncbi.nlm.nih.gov/pubmed/30813483 http://dx.doi.org/10.3390/ijms20040985 |
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