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Molecular Prerequisites for Diminished Cold Sensitivity in Ground Squirrels and Hamsters

  • Vanessa Matos-Cruz
  • , Eve R. Schneider
  • , Marco Mastrotto
  • , Dana K. Merriman
  • , Sviatoslav N. Bagriantsev
  • , Elena O. Gracheva

Producción científica: Articlerevisión exhaustiva

81 Citas (Scopus)

Resumen

Thirteen-lined ground squirrels and Syrian hamsters are known for their ability to withstand cold during hibernation. We found that hibernators exhibit cold tolerance even in the active state. Imaging and electrophysiology of squirrel somatosensory neurons reveal a decrease in cold sensitivity of TRPM8-expressing cells. Characterization of squirrel and hamster TRPM8 showed that the channels are chemically activated but exhibit poor activation by cold. Cold sensitivity can be re-introduced into squirrel and hamster TRPM8 by transferring the transmembrane domain from the cold sensitive rat ortholog. The same can be achieved in squirrel TRPM8 by mutating only six amino acids. Reciprocal mutations suppress cold sensitivity of the rat ortholog, supporting functional significance of these residues. Our results suggest that ground squirrels and hamsters exhibit reduced cold sensitivity, partially due to modifications in the transmembrane domain of TRPM8. Our study reveals molecular adaptations that accompany cold tolerance in two species of mammalian hibernators. Matos-Cruz et al. show that ground squirrels and hamsters exhibit cold tolerance even in the active non-hibernating state, partially due to independent modifications in the core transmembrane domain of the cold-sensing channel, TRPM8. The study reveals molecular adaptations that accompany cold tolerance in two species of active mammalian hibernators.

Idioma originalEnglish
Páginas (desde-hasta)3329-3337
Número de páginas9
PublicaciónCell Reports
Volumen21
N.º12
DOI
EstadoPublished - dic 19 2017

Nota bibliográfica

Publisher Copyright:
© 2017 The Author(s)

Financiación

We thank members of the Gracheva and Bagriantsev laboratories for their contributions throughout the project. This study was partly funded by fellowships from the Beckman Foundation and the Rita Allen Foundation and NIH grants 1R01NS091300-01A1 and 3R01NS091300-02S1 to E.O.G; by American Heart Association grant 14SDG17880015 and NSF grant 1453167 to S.N.B.; and by the Axle Tech International Endowed Professorship to D.K.M. V.M.-C. was partially supported by an NSF Postdoctoral Fellowship ( 1306144 ). E.R.S. was supported by a postdoctoral fellowship from the Arnold and Mabel Beckman Foundation .

FinanciadoresNúmero del financiador
Arnold and Mabel Beckman Foundation
National Science Foundation Arctic Social Science Program1453167, 1306144
National Institutes of Health (NIH)
Institute of Neurological Disorders and Stroke National Advisory Neurological Disorders and Stroke CouncilR01NS091300
American the American Heart Association14SDG17880015
Arnold and Mabel Beckman Foundation
Rita Allen Foundation

    ASJC Scopus subject areas

    • General Biochemistry, Genetics and Molecular Biology

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