Mouse transient receptor potential melastatin 2 (TRPM2) isoform 7 attenuates full‐length mouse TRPM2 activity through reductions in its expression by targeting it to ER‐associated degradation

Abstract

AbstractTransient receptor potential melastatin 2 (TRPM2) assembles into tetramers to function as an oxidative stress‐sensitive Ca2+ channel at the surface membrane. Limited information is currently available on the 10 protein isoforms of mouse TRPM2 (mTRPM2) identified. This study investigated whether these isoforms function as Ca2+ channels and examined their effects on full‐length mTRPM2 activity using the HEK 293 cell exogenous expression system. Only full‐length mTRPM2, isoform 1 localized to the surface membrane and was activated by oxidative stress. Isoform 7 was clearly recognized by protein quality control systems and degraded by endoplasmic reticulum‐associated degradation after transmembrane proteolysis. In the co‐expression system, the activation and expression of full‐length mTRPM2 were attenuated by its co‐expression with isoform 7, but not with the other isoforms. This decrease in the expression of full‐length mTRPM2 was recovered by the proteasomal inhibitor. The present results suggest that isoforms other than isoform 1 did not function as oxidative stress‐sensitive channels and also that only isoform 7 attenuated the activation of full‐length mTRPM2 by targeting it to endoplasmic reticulum‐associated degradation. The present study will provide important information on the functional nature of mTRPM2 isoforms for the elucidation of their roles in physiological and patho‐physiological responses in vivo using mouse models.