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PKCα and PKCδ: Friends and Rivals

PKC comprises a large family of serine/threonine kinases that share a requirement for allosteric activation by lipids. While PKC isoforms have significant homology, functional divergence is evident among subfamilies and between individual PKC isoforms within a subfamily. Here, we highlight these dif...

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Autores principales: Black, Jennifer D., Affandi, Trisiani, Black, Adrian R., Reyland, Mary E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Biochemistry and Molecular Biology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9352922/
https://www.ncbi.nlm.nih.gov/pubmed/35760100
http://dx.doi.org/10.1016/j.jbc.2022.102194
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author Black, Jennifer D.
Affandi, Trisiani
Black, Adrian R.
Reyland, Mary E.
author_facet Black, Jennifer D.
Affandi, Trisiani
Black, Adrian R.
Reyland, Mary E.
author_sort Black, Jennifer D.
collection PubMed
description PKC comprises a large family of serine/threonine kinases that share a requirement for allosteric activation by lipids. While PKC isoforms have significant homology, functional divergence is evident among subfamilies and between individual PKC isoforms within a subfamily. Here, we highlight these differences by comparing the regulation and function of representative PKC isoforms from the conventional (PKCα) and novel (PKCδ) subfamilies. We discuss how unique structural features of PKCα and PKCδ underlie differences in activation and highlight the similar, divergent, and even opposing biological functions of these kinases. We also consider how PKCα and PKCδ can contribute to pathophysiological conditions and discuss challenges to targeting these kinases therapeutically.
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spelling pubmed-93529222022-08-09 PKCα and PKCδ: Friends and Rivals Black, Jennifer D. Affandi, Trisiani Black, Adrian R. Reyland, Mary E. J Biol Chem JBC Reviews PKC comprises a large family of serine/threonine kinases that share a requirement for allosteric activation by lipids. While PKC isoforms have significant homology, functional divergence is evident among subfamilies and between individual PKC isoforms within a subfamily. Here, we highlight these differences by comparing the regulation and function of representative PKC isoforms from the conventional (PKCα) and novel (PKCδ) subfamilies. We discuss how unique structural features of PKCα and PKCδ underlie differences in activation and highlight the similar, divergent, and even opposing biological functions of these kinases. We also consider how PKCα and PKCδ can contribute to pathophysiological conditions and discuss challenges to targeting these kinases therapeutically. American Society for Biochemistry and Molecular Biology 2022-06-24 /pmc/articles/PMC9352922/ /pubmed/35760100 http://dx.doi.org/10.1016/j.jbc.2022.102194 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle JBC Reviews
Black, Jennifer D.
Affandi, Trisiani
Black, Adrian R.
Reyland, Mary E.
PKCα and PKCδ: Friends and Rivals
title PKCα and PKCδ: Friends and Rivals
title_full PKCα and PKCδ: Friends and Rivals
title_fullStr PKCα and PKCδ: Friends and Rivals
title_full_unstemmed PKCα and PKCδ: Friends and Rivals
title_short PKCα and PKCδ: Friends and Rivals
title_sort pkcα and pkcδ: friends and rivals
topic JBC Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9352922/
https://www.ncbi.nlm.nih.gov/pubmed/35760100
http://dx.doi.org/10.1016/j.jbc.2022.102194
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