Published January 2018 | Version v1
Journal article

Involvement of TRPV3 and TRPM8 ion channel proteins in induction of mammalian cold-inducible proteins

  • 1. Department of Clinical Molecular Biology, Graduate School of Medicine, Kyoto University, 54 Shogoin Kawahara-cho, Sakyo-ku, Kyoto 606-8507 (Japan)
  • 2. Department of Urology, Faculty of Medicine, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki 305-8575 (Japan)
  • 3. Department of Molecular and Cellular Neurobiology, Gunma University Graduate School of Medicine, Maebashi 371-8511 (Japan)
  • 4. Department of Radiation Genetics, Graduate School of Medicine, Kyoto University, Yoshida Konoe, Sakyo-ku, Kyoto 606-8501 (Japan)

Description

Highlights: • CIRP, RBM3 and SRSF5 could be induced by mild hypothermia in the absence of TRPV4. • TRPV3 and TRPM8 as well as TRPV4 are involved in induction of CIRP, RBM3 and SRSF5. • Activity to induce CIRP, RBM3 and SRSF5 seems independent of TRP ion channel activity. 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.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.bbrc.2017.11.136

Additional details

Identifiers

DOI
10.1016/j.bbrc.2017.11.136;
PII
S0006291X1732315X;

Publishing Information

Journal Title
Biochemical and Biophysical Research Communications
Journal Volume
495
Journal Issue
1
Journal Page Range
p. 935-940
ISSN
0006-291X
CODEN
BBRCA9

INIS

Country of Publication
United States
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
53051699
Subject category
S60: APPLIED LIFE SCIENCES;
Descriptors DEI
ARGININE; HYPOTHERMIA; LUNGS; MICE; RECEPTORS; RNA; SERINE
Descriptors DEC
AMINO ACIDS; ANIMALS; BODY; BODY TEMPERATURE; CARBOXYLIC ACIDS; HYDROXY ACIDS; MAMMALS; MEMBRANE PROTEINS; NUCLEIC ACIDS; ORGANIC ACIDS; ORGANIC COMPOUNDS; ORGANS; PROTEINS; RESPIRATORY SYSTEM; RODENTS; VERTEBRATES

Optional Information

Copyright
Copyright (c) 2017 The Authors. Published by Elsevier Inc.