Protein Translation and Signaling in Human Eosinophils

We have recently reported that, unlike IL-5 and GM-CSF, IL-3 induces increased translation of a subset of mRNAs. In addition, we have demonstrated that Pin1 controls the activity of mRNA binding proteins, leading to enhanced mRNA stability, GM-CSF protein production and prolonged eosinophil (EOS) su...

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Main Authors: Stephane Esnault, Zhong-Jian Shen, James S. Malter
Format: Article
Language:English
Published: Frontiers Media S.A. 2017-09-01
Series:Frontiers in Medicine
Subjects:
Online Access:http://journal.frontiersin.org/article/10.3389/fmed.2017.00150/full
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spelling doaj-7bd618711b9e44558ea83645e81441e22020-11-24T22:17:44ZengFrontiers Media S.A.Frontiers in Medicine2296-858X2017-09-01410.3389/fmed.2017.00150273865Protein Translation and Signaling in Human EosinophilsStephane Esnault0Zhong-Jian Shen1James S. Malter2Department of Medicine, Allergy, Pulmonary, and Critical Care Medicine Division, University of Wisconsin-Madison School of Medicine and Public Health, Madison, WI, United StatesDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, United StatesDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, United StatesWe have recently reported that, unlike IL-5 and GM-CSF, IL-3 induces increased translation of a subset of mRNAs. In addition, we have demonstrated that Pin1 controls the activity of mRNA binding proteins, leading to enhanced mRNA stability, GM-CSF protein production and prolonged eosinophil (EOS) survival. In this review, discussion will include an overview of cap-dependent protein translation and its regulation by intracellular signaling pathways. We will address the more general process of mRNA post-transcriptional regulation, especially regarding mRNA binding proteins, which are critical effectors of protein translation. Furthermore, we will focus on (1) the roles of IL-3-driven sustained signaling on enhanced protein translation in EOS, (2) the mechanisms regulating mRNA binding proteins activity in EOS, and (3) the potential targeting of IL-3 signaling and the signaling leading to mRNA binding activity changes to identify therapeutic targets to treat EOS-associated diseases.http://journal.frontiersin.org/article/10.3389/fmed.2017.00150/fulleosinophilsprotein translationribosomal S6 proteinPin-1IL-3intracellular signaling
collection DOAJ
language English
format Article
sources DOAJ
author Stephane Esnault
Zhong-Jian Shen
James S. Malter
spellingShingle Stephane Esnault
Zhong-Jian Shen
James S. Malter
Protein Translation and Signaling in Human Eosinophils
Frontiers in Medicine
eosinophils
protein translation
ribosomal S6 protein
Pin-1
IL-3
intracellular signaling
author_facet Stephane Esnault
Zhong-Jian Shen
James S. Malter
author_sort Stephane Esnault
title Protein Translation and Signaling in Human Eosinophils
title_short Protein Translation and Signaling in Human Eosinophils
title_full Protein Translation and Signaling in Human Eosinophils
title_fullStr Protein Translation and Signaling in Human Eosinophils
title_full_unstemmed Protein Translation and Signaling in Human Eosinophils
title_sort protein translation and signaling in human eosinophils
publisher Frontiers Media S.A.
series Frontiers in Medicine
issn 2296-858X
publishDate 2017-09-01
description We have recently reported that, unlike IL-5 and GM-CSF, IL-3 induces increased translation of a subset of mRNAs. In addition, we have demonstrated that Pin1 controls the activity of mRNA binding proteins, leading to enhanced mRNA stability, GM-CSF protein production and prolonged eosinophil (EOS) survival. In this review, discussion will include an overview of cap-dependent protein translation and its regulation by intracellular signaling pathways. We will address the more general process of mRNA post-transcriptional regulation, especially regarding mRNA binding proteins, which are critical effectors of protein translation. Furthermore, we will focus on (1) the roles of IL-3-driven sustained signaling on enhanced protein translation in EOS, (2) the mechanisms regulating mRNA binding proteins activity in EOS, and (3) the potential targeting of IL-3 signaling and the signaling leading to mRNA binding activity changes to identify therapeutic targets to treat EOS-associated diseases.
topic eosinophils
protein translation
ribosomal S6 protein
Pin-1
IL-3
intracellular signaling
url http://journal.frontiersin.org/article/10.3389/fmed.2017.00150/full
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AT zhongjianshen proteintranslationandsignalinginhumaneosinophils
AT jamessmalter proteintranslationandsignalinginhumaneosinophils
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