TY - JOUR
T1 - Protein translation and signaling in human eosinophils
AU - Esnault, Stephane
AU - Shen, Zhong Jian
AU - Malter, James S.
N1 - Funding Information:
This work was supported by P01 HL088594 and Clinical and Translational Research Center grant UL1 RR025011 from the National Institutes of Health.
Publisher Copyright:
© 2017 Esnault, Shen and Malter.
PY - 2017
Y1 - 2017
N2 - 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.
AB - 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.
KW - Eosinophils
KW - IL-3
KW - Intracellular signaling
KW - Pin-1
KW - Protein translation
KW - Ribosomal S6 protein
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U2 - 10.3389/fmed.2017.00150
DO - 10.3389/fmed.2017.00150
M3 - Review article
C2 - 28971096
AN - SCOPUS:85048015777
SN - 2296-858X
VL - 4
JO - Frontiers in Medicine
JF - Frontiers in Medicine
IS - SEP
M1 - 150
ER -