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The Jak/Stat Signaling Pathway Is Downregulated at Febrile Temperatures

BACKGROUND: The Janus family of kinases (JAKs), Jak1, Jak2, Jak3, and Tyk2, constitute a subgroup of non-receptor protein tyrosine kinases. Upon cytokine binding, the receptor-associated kinases are activated and phosphorylate tyrosine residues in their cognate cytokine receptors. Their activities a...

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Autores principales: Nespital, Tobias, Strous, Ger J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3498154/
https://www.ncbi.nlm.nih.gov/pubmed/23166650
http://dx.doi.org/10.1371/journal.pone.0049374
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author Nespital, Tobias
Strous, Ger J.
author_facet Nespital, Tobias
Strous, Ger J.
author_sort Nespital, Tobias
collection PubMed
description BACKGROUND: The Janus family of kinases (JAKs), Jak1, Jak2, Jak3, and Tyk2, constitute a subgroup of non-receptor protein tyrosine kinases. Upon cytokine binding, the receptor-associated kinases are activated and phosphorylate tyrosine residues in their cognate cytokine receptors. Their activities are controlled at several levels and include cellular concentration, auto-activation, and degradation. PRINCIPAL FINDINGS: Our findings show that elevated temperatures in the fever range irreversibly aggregate Jak2 and considerably reduce functional Jak2 protein levels. Jak2 synthesis remains unaltered. We observed that also the protein level of the signal transducer and activator of transcription, STAT5b, is transiently decreased at temperatures above 37°C. Consequently, the signaling response, e.g. via the growth hormone receptor, is reduced. CONCLUSIONS/SIGNIFICANCE: These findings predict that elevated body temperatures lower the responsiveness of cytokine receptors.
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spelling pubmed-34981542012-11-19 The Jak/Stat Signaling Pathway Is Downregulated at Febrile Temperatures Nespital, Tobias Strous, Ger J. PLoS One Research Article BACKGROUND: The Janus family of kinases (JAKs), Jak1, Jak2, Jak3, and Tyk2, constitute a subgroup of non-receptor protein tyrosine kinases. Upon cytokine binding, the receptor-associated kinases are activated and phosphorylate tyrosine residues in their cognate cytokine receptors. Their activities are controlled at several levels and include cellular concentration, auto-activation, and degradation. PRINCIPAL FINDINGS: Our findings show that elevated temperatures in the fever range irreversibly aggregate Jak2 and considerably reduce functional Jak2 protein levels. Jak2 synthesis remains unaltered. We observed that also the protein level of the signal transducer and activator of transcription, STAT5b, is transiently decreased at temperatures above 37°C. Consequently, the signaling response, e.g. via the growth hormone receptor, is reduced. CONCLUSIONS/SIGNIFICANCE: These findings predict that elevated body temperatures lower the responsiveness of cytokine receptors. Public Library of Science 2012-11-14 /pmc/articles/PMC3498154/ /pubmed/23166650 http://dx.doi.org/10.1371/journal.pone.0049374 Text en © 2012 Nespital, Strous http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Nespital, Tobias
Strous, Ger J.
The Jak/Stat Signaling Pathway Is Downregulated at Febrile Temperatures
title The Jak/Stat Signaling Pathway Is Downregulated at Febrile Temperatures
title_full The Jak/Stat Signaling Pathway Is Downregulated at Febrile Temperatures
title_fullStr The Jak/Stat Signaling Pathway Is Downregulated at Febrile Temperatures
title_full_unstemmed The Jak/Stat Signaling Pathway Is Downregulated at Febrile Temperatures
title_short The Jak/Stat Signaling Pathway Is Downregulated at Febrile Temperatures
title_sort jak/stat signaling pathway is downregulated at febrile temperatures
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3498154/
https://www.ncbi.nlm.nih.gov/pubmed/23166650
http://dx.doi.org/10.1371/journal.pone.0049374
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