Identification of a transient receptor potential channel that is regulated by phospholipid asymmetry

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Abstract
: Phospholipid asymmetry is a hallmark of mammalian cell membranes and reflects the selective distribution of distinct phospholipid species between the two leaflets of the lipid bilayer. Although this asymmetry is tightly maintained, the membrane proteins whose functions depend on it remain largely unknown. To perturb phospholipid asymmetry experimentally, we expressed a constitutively active phospholipid scramblase and thereby identified transient receptor potential melastatin 8 (TRPM8) as an ion channel regulated by this membrane property. Activation of TRPM8 by both l -menthol and innocuous cold was markedly suppressed following disruption of phospholipid asymmetry. Likewise, selective depletion of phosphatidylserine (PS), a phospholipid enriched in the cytoplasmic leaflet, using a cytosolically targeted PS decarboxylase attenuated TRPM8 activation, indicating that cytoplasmic PS is required for proper TRPM8 function. Mechanistically, our findings suggest that cytoplasmic PS supports efficient TRPM8 activation by maintaining the biochemical state of the channel. Together, these findings identify TRPM8 as a phospholipid asymmetry-dependent ion channel and establish an experimental strategy for systematically identifying membrane proteins regulated by phospholipid asymmetry. This work provides a foundation for future studies investigating the biological significance of this fundamental membrane property.
Funding Information
  • Grant-in-Aid for Scientific Research KAKENHI (22H03484)
  • Grant-in-Aid for Scientific Research KAKENHI (25K02994)
  • Grant-in-Aid for Scientific Research KAKENHI (22K20636)
  • Grant-in-Aid for Scientific Research KAKENHI (23K14184)
  • Grant-in-Aid for Scientific Research KAKENHI (25K18466)
  • Grant-in-Aid for Transformative Research Areas B (23H03854)
  • Grant-in-Aid for Transformative Research Areas B (23H03856)
  • Intramural Research Grant for Neurological and Psychiatric Disorder of NCNP (8-13)
  • Takeda Science Foundation
  • Ono Medical Research Foundation
  • Uehara Memorial Foundation
  • Chugai Foundation for Innovative Drug Discovery Science
  • Ube Foundation

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