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SOCS3: An essential physiological inhibitor of signaling by interleukin-6 and G-CSF family cytokines

SOCS3 is an inducible negative feedback inhibitor of cytokine signaling. Conditional deletion of SOCS3 in mice using the Cre-lox system has now been applied to a range of cell types in the steady-state and under inflammatory, pathogenic, or tumorigenic stress, with the resulting phenotypes demonstra...

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Detalles Bibliográficos
Autores principales: White, Christine A, Nicola, Nicos A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3876435/
https://www.ncbi.nlm.nih.gov/pubmed/24416642
http://dx.doi.org/10.4161/jkst.25045
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author White, Christine A
Nicola, Nicos A
author_facet White, Christine A
Nicola, Nicos A
author_sort White, Christine A
collection PubMed
description SOCS3 is an inducible negative feedback inhibitor of cytokine signaling. Conditional deletion of SOCS3 in mice using the Cre-lox system has now been applied to a range of cell types in the steady-state and under inflammatory, pathogenic, or tumorigenic stress, with the resulting phenotypes demonstrating the effects of SOCS3 in physiological and disease contexts. Together with recent structural and biochemical studies on the mechanisms of SOCS3 binding to cytokine receptors and associated kinases, we now have a better understanding of the non-redundant roles of SOCS3 in the inhibition of cytokine signaling via the receptors gp130, G-CSFR, leptinR, and IL-12Rβ. This review discusses the known functional activities of SOCS3 in fertility and development, inflammation, innate and adaptive immunity, and malignancy as determined by genetic studies in mice.
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spelling pubmed-38764352014-01-10 SOCS3: An essential physiological inhibitor of signaling by interleukin-6 and G-CSF family cytokines White, Christine A Nicola, Nicos A JAKSTAT Review SOCS3 is an inducible negative feedback inhibitor of cytokine signaling. Conditional deletion of SOCS3 in mice using the Cre-lox system has now been applied to a range of cell types in the steady-state and under inflammatory, pathogenic, or tumorigenic stress, with the resulting phenotypes demonstrating the effects of SOCS3 in physiological and disease contexts. Together with recent structural and biochemical studies on the mechanisms of SOCS3 binding to cytokine receptors and associated kinases, we now have a better understanding of the non-redundant roles of SOCS3 in the inhibition of cytokine signaling via the receptors gp130, G-CSFR, leptinR, and IL-12Rβ. This review discusses the known functional activities of SOCS3 in fertility and development, inflammation, innate and adaptive immunity, and malignancy as determined by genetic studies in mice. Landes Bioscience 2013-10-01 2013-06-11 /pmc/articles/PMC3876435/ /pubmed/24416642 http://dx.doi.org/10.4161/jkst.25045 Text en Copyright © 2013 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Review
White, Christine A
Nicola, Nicos A
SOCS3: An essential physiological inhibitor of signaling by interleukin-6 and G-CSF family cytokines
title SOCS3: An essential physiological inhibitor of signaling by interleukin-6 and G-CSF family cytokines
title_full SOCS3: An essential physiological inhibitor of signaling by interleukin-6 and G-CSF family cytokines
title_fullStr SOCS3: An essential physiological inhibitor of signaling by interleukin-6 and G-CSF family cytokines
title_full_unstemmed SOCS3: An essential physiological inhibitor of signaling by interleukin-6 and G-CSF family cytokines
title_short SOCS3: An essential physiological inhibitor of signaling by interleukin-6 and G-CSF family cytokines
title_sort socs3: an essential physiological inhibitor of signaling by interleukin-6 and g-csf family cytokines
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3876435/
https://www.ncbi.nlm.nih.gov/pubmed/24416642
http://dx.doi.org/10.4161/jkst.25045
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