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p66Shc in Cardiovascular Pathology

p66Shc is a widely expressed protein that governs a variety of cardiovascular pathologies by generating, and exacerbating, pro-apoptotic ROS signals. Here, we review p66Shc’s connections to reactive oxygen species, expression, localization, and discuss p66Shc signaling and mitochondrial functions. E...

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Detalles Bibliográficos
Autores principales: Haslem, Landon, Hays, Jennifer M., Hays, Franklin A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9180016/
https://www.ncbi.nlm.nih.gov/pubmed/35681549
http://dx.doi.org/10.3390/cells11111855
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author Haslem, Landon
Hays, Jennifer M.
Hays, Franklin A.
author_facet Haslem, Landon
Hays, Jennifer M.
Hays, Franklin A.
author_sort Haslem, Landon
collection PubMed
description p66Shc is a widely expressed protein that governs a variety of cardiovascular pathologies by generating, and exacerbating, pro-apoptotic ROS signals. Here, we review p66Shc’s connections to reactive oxygen species, expression, localization, and discuss p66Shc signaling and mitochondrial functions. Emphasis is placed on recent p66Shc mitochondrial function discoveries including structure/function relationships, ROS identity and regulation, mechanistic insights, and how p66Shc-cyt c interactions can influence p66Shc mitochondrial function. Based on recent findings, a new p66Shc mitochondrial function model is also put forth wherein p66Shc acts as a rheostat that can promote or antagonize apoptosis. A discussion of how the revised p66Shc model fits previous findings in p66Shc-mediated cardiovascular pathology follows.
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spelling pubmed-91800162022-06-10 p66Shc in Cardiovascular Pathology Haslem, Landon Hays, Jennifer M. Hays, Franklin A. Cells Review p66Shc is a widely expressed protein that governs a variety of cardiovascular pathologies by generating, and exacerbating, pro-apoptotic ROS signals. Here, we review p66Shc’s connections to reactive oxygen species, expression, localization, and discuss p66Shc signaling and mitochondrial functions. Emphasis is placed on recent p66Shc mitochondrial function discoveries including structure/function relationships, ROS identity and regulation, mechanistic insights, and how p66Shc-cyt c interactions can influence p66Shc mitochondrial function. Based on recent findings, a new p66Shc mitochondrial function model is also put forth wherein p66Shc acts as a rheostat that can promote or antagonize apoptosis. A discussion of how the revised p66Shc model fits previous findings in p66Shc-mediated cardiovascular pathology follows. MDPI 2022-06-06 /pmc/articles/PMC9180016/ /pubmed/35681549 http://dx.doi.org/10.3390/cells11111855 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Haslem, Landon
Hays, Jennifer M.
Hays, Franklin A.
p66Shc in Cardiovascular Pathology
title p66Shc in Cardiovascular Pathology
title_full p66Shc in Cardiovascular Pathology
title_fullStr p66Shc in Cardiovascular Pathology
title_full_unstemmed p66Shc in Cardiovascular Pathology
title_short p66Shc in Cardiovascular Pathology
title_sort p66shc in cardiovascular pathology
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9180016/
https://www.ncbi.nlm.nih.gov/pubmed/35681549
http://dx.doi.org/10.3390/cells11111855
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