| First Author | Das R | Year | 2019 |
| Journal | Biochem Biophys Res Commun | Volume | 517 |
| Issue | 4 | Pages | 566-574 |
| PubMed ID | 31387748 | Mgi Jnum | J:291721 |
| Mgi Id | MGI:6443132 | Doi | 10.1016/j.bbrc.2019.07.042 |
| Citation | Das R, et al. (2019) TRPV4 expresses in bone cell lineages and TRPV4-R616Q mutant causing Brachyolmia in human reveals "loss-of-interaction" with cholesterol. Biochem Biophys Res Commun 517(4):566-574 |
| abstractText | Transient receptor potential Vanilloid ion channel sub type 4 (TRPV4) is involved in complex Ca(2+)-signaling. At least one copy of TRPV4 is present in all vertebrates and is involved in several physiological processes including sensory process and point mutations in TRPV4 leads to development of different pathophysiological disorders in human. R616Q mutant of TRPV4 has been referred as "gain-of-function" mutant causing abnormality in bone cells and develop pathophysiological condition known as "Brachyolmia". In this work, we demonstrated that R616Q mutation is located in a very critical position of TRPV4 containing a cholesterol-binding motif sequence which is highly conserved in all vertebrates. Accordingly, TRPV4-Wt but not the TRPV4-R616Q localizes preferably in cholesterol-enriched lipid rafts in osteogenic cell line Saos2 and in DRG-neuron derived F11cell line. Further, FRAP experiment suggest TRPV4-Wt but not the TRPV4-R616Q mutant is more mobile especially in cholesterol-reduced lipid membrane. GST-tagged TM4-Loop-TM5 fragment containing TRPV4-Wt but not R616Q sequence interacts with cholesterol, forms high-molecular weight complex and also show band shift in SDS-PAGE. TRPV4 is expressed in Mesenchymal stem cells and the localization of TRPV4 in lipid raft is dependent on temperature and cholesterol. Our data suggests that TRPV4-R616Q mutant behaves as a "loss-of-interaction" with cholesterol. |
