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Title: Involvement of TRPV3 and TRPM8 ion channel proteins in induction of mammalian cold-inducible proteins
Authors: Fujita, Takanori
Liu, Yu
Higashitsuji, Hiroaki
Itoh, Katsuhiko  kyouindb  KAKEN_id
Shibasaki, Koji
Fujita, Jun
Nishiyama, Hiroyuki
Author's alias: 伊藤, 克彦
藤田, 潤
Keywords: TRP channel
Cold-inducible
RNA-binding protein
RBM3
SRSF5
Hypothermia
Issue Date: 1-Jan-2018
Publisher: Elsevier BV
Journal title: Biochemical and Biophysical Research Communications
Volume: 495
Issue: 1
Start page: 935
End page: 940
Abstract: Cold-inducible RNA-binding protein (CIRP), RNA-binding motif protein 3 (RBM3) and serine and arginine rich splicing factor 5 (SRSF5) are RNA-binding proteins that are transcriptionally upregulated in response to moderately low temperatures and a variety of cellular stresses in mammalian cells. Induction of these cold-inducible proteins (CIPs) is dependent on transient receptor potential (TRP) V4 channel protein, but seems independent of its ion channel activity. We herein report that in addition to TRPV4, TRPV3 and TRPM8 are necessary for the induction of CIPs. We established cell lines from the lung of TRPV4-knockout (KO) mouse, and observed induction of CIPs in them by western blot analysis. A TRPV4 antagonist RN1734 suppressed the induction in wild-type mouse cells, but not in TRPV4-KO cells. A TRPV3 channel blocker S408271 and a TRPM8 channel blocker AMTB as well as siRNAs against TRPV3 and TRPM8 suppressed the CIP induction in mouse TRPV4-KO cells and human U-2 OS cells. A TRPV3 channel agonist 2-APB induced CIP expression, but camphor did not. Neither did a TRPM8 channel agonist WS-12. These results suggest that TRPV4, TRPV3 and TRPM8 proteins, but not their ion channel activities are necessary for the induction of CIPs at 32 °C. Identification of proteins that differentially interact with these TRP channels at 37 °C and 32 °C would help elucidate the underlying mechanisms of CIP induction by hypothermia.
Rights: © 2017 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
URI: http://hdl.handle.net/2433/230795
DOI(Published Version): 10.1016/j.bbrc.2017.11.136
PubMed ID: 29175331
Appears in Collections:Journal Articles

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