@article{91913018459642e1bfcf752128719c6c,
title = "Thermosensitive TRPV4 channels mediate temperature-dependent microglia movement",
abstract = "Microglia maintain central nervous system homeostasis by monitoring changes in their environment (resting state) and by taking protective actions to equilibrate such changes (activated state). These surveillance and protective roles both require constant movement of microglia. Interestingly, induced hypothermia can reduce microglia migration caused by ischemia, suggesting that microglia movement can be modulated by temperature. Although several ion channels and transporters are known to support microglia movement, the precise molecular mechanism that regulates temperature-dependent movement of microglia remains unclear. Some members of the transient receptor potential (TRP) channel superfamily exhibit thermosensitivity and thus are strong candidates for mediation of this phenomenon. Here, we demonstrate that mouse microglia exhibit temperature-dependent movement in vitro and in vivo that is mediated by TRPV4 channels within the physiological range of body temperature. Our findings may provide a basis for future research into the potential clinical application of temperature regulation to preserve cell function via manipulation of ion channel activity.",
keywords = "Microglia, Movement, TRP channels, TRPV4",
author = "Rei Nishimoto and Sandra Derouiche and Kei Eto and Aykut Deveci and Makiko Kashio and Yoshitaka Kimori and Yoshikazu Matsuoka and Hiroshi Morimatsu and Junichi Nabekura and Makoto Tominaga",
note = "Funding Information: ACKNOWLEDGMENTS. We thank D. Julius (University of California, San Francisco), Y. Mori (Kyoto University), and M. Suzuki (Jichi Medical School) for providing knockout mice; M. Caterina (Johns Hopkins University) and V. Flockerzi (Universit{\"a}t des Saarlandes, Germany) for expression vectors; K. Ikenaka (National Institute for Physiological Sciences) for helpful suggestions; and N. Fukuta, C. Saito, K. Fukuoka, and T. Hashimoto (National Institute for Physiological Sciences) for generation of M2KO and V4KO-Iba1-EGFP mice. This work was completed in a partial fulfillment of a Ph.D. degree to R.N. at The Graduate University for Advanced Studies, SOKENDAI. This work was supported by a Japan Society for the Promotion of Science KAKENHI Grant-in-Aid for Young Scientists (B) Grant and the Cooperative Study Program of the National Institute for Physiological Sciences (to R.N.) to a Ministry of Education, Culture, Sports, Science and Technology KAKENHI Grant-in-Aid for Scientific Research Grant and Scientific Research on Innovative Areas “Thermal Biology” (to M.T.) and Advanced Bioimaging Support (to M.T.). Publisher Copyright: {\textcopyright} 2021 National Academy of Sciences. All rights reserved.",
year = "2021",
month = apr,
day = "27",
doi = "10.1073/pnas.2012894118",
language = "English",
volume = "118",
journal = "Proceedings of the National Academy of Sciences of the United States of America",
issn = "0027-8424",
publisher = "National Academy of Sciences",
number = "17",
}