| First Author | Zhao Q | Year | 2020 |
| Journal | Sci Rep | Volume | 10 |
| Issue | 1 | Pages | 20719 |
| PubMed ID | 33244095 | Mgi Jnum | J:299699 |
| Mgi Id | MGI:6491043 | Doi | 10.1038/s41598-020-77620-y |
| Citation | Zhao Q, et al. (2020) TRPM2 promotes autophagic degradation in vascular smooth muscle cells. Sci Rep 10(1):20719 |
| abstractText | Transient receptor potential channel M2 (TRPM2) is a Ca(2+)-permeable channel that is activated by reactive oxygen species (ROS). In many cell types, ROS activate TRPM2 to induce excessive Ca(2+) influx, resulting in Ca(2+) overload and consequent cell death. Recent studies suggest that TRPM2 may also regulate autophagy in pericytes and cancer cells by acting on the early step of autophagy, i.e. autophagic induction. However, there is no report on the role of TRPM2 in autophagic degradation, which is the late stage of autophagy. In the present study, we found abundant TRPM2 expression in lysosomes/autolysosomes in the primary cultured mouse aortic smooth muscle cells (mASMCs). Nutrient starvation stimulated autophagic flux in mASMCs mainly by promoting autophagic degradation. This starvation-induced autophagic degradation was reduced by TRPM2 knockout. Importantly, starvation-induced lysosomal/autolysosomal acidification and cell death were also substantially reduced by TRPM2 knockout. Taken together, the present study uncovered a novel mechanism that lysosomal TRPM2 facilitates lysosomal acidification to stimulate excessive autolysosome degradation and consequent cell death. |
