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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...

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Autores principales: Ciciliot, Stefano, Fadini, Gian Paolo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
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.
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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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