| First Author | Beesetty P | Year | 2018 |
| Journal | Sci Rep | Volume | 8 |
| Issue | 1 | Pages | 3023 |
| PubMed ID | 29445164 | Mgi Jnum | J:262737 |
| Mgi Id | MGI:6162874 | Doi | 10.1038/s41598-018-21004-w |
| Citation | Beesetty P, et al. (2018) Inactivation of TRPM7 kinase in mice results in enlarged spleens, reduced T-cell proliferation and diminished store-operated calcium entry. Sci Rep 8(1):3023 |
| abstractText | T lymphocytes enlarge (blast) and proliferate in response to antigens in a multistep program that involves obligatory cytosolic calcium elevations. Store-operated calcium entry (SOCE) pathway is the primary source of Ca(2+) in these cells. Here, we describe a novel modulator of blastogenesis, proliferation and SOCE: the TRPM7 channel kinase. TRPM7 kinase-dead (KD) K1646R knock-in mice exhibited splenomegaly and impaired blastogenic responses elicited by PMA/ionomycin or anti-CD3/CD28 antibodies. Splenic T-cell proliferation in vitro was weaker in the mutant compared to wildtype littermates. TRPM7 current magnitudes in WT and KD mouse T cells were, however, similar. We tested the dependence of T-cell proliferation on external Ca(2+) and Mg(2+) concentrations. At a fixed [Mg(2+)o] of ~0.4 mM, Ca(2+)o stimulated proliferation with a steep concentration dependence and vice versa, at a fixed [Ca(2+)o] of ~0.4 mM, Mg(2+)o positively regulated proliferation but with a shallower dependence. Proliferation was significantly lower in KD mouse than in wildtype at all Ca(2+) and Mg(2+) concentrations. Ca(2+) elevations elicited by anti-CD3 antibody were diminished in KD mutant T cells and SOCE measured in activated KD splenocytes was reduced. These results demonstrate that a functional TRPM7 kinase supports robust SOCE, blastogenesis and proliferation, whereas its inactivation suppresses these cellular events. |
