| First Author | Diercks BP | Year | 2018 |
| Journal | Sci Signal | Volume | 11 |
| Issue | 561 | PubMed ID | 30563862 |
| Mgi Jnum | J:284476 | Mgi Id | MGI:6381339 |
| Doi | 10.1126/scisignal.aat0358 | Citation | Diercks BP, et al. (2018) ORAI1, STIM1/2, and RYR1 shape subsecond Ca(2+) microdomains upon T cell activation. Sci Signal 11(561) |
| abstractText | The earliest intracellular signals that occur after T cell activation are local, subsecond Ca(2+) microdomains. Here, we identified a Ca(2+) entry component involved in Ca(2+) microdomain formation in both unstimulated and stimulated T cells. In unstimulated T cells, spontaneously generated small Ca(2+) microdomains required ORAI1, STIM1, and STIM2. Super-resolution microscopy of unstimulated T cells identified a circular subplasmalemmal region with a diameter of about 300 nm with preformed patches of colocalized ORAI1, ryanodine receptors (RYRs), and STIM1. Preformed complexes of STIM1 and ORAI1 in unstimulated cells were confirmed by coimmunoprecipitation and Forster resonance energy transfer studies. Furthermore, within the first second after T cell receptor (TCR) stimulation, the number of Ca(2+) microdomains increased in the subplasmalemmal space, an effect that required ORAI1, STIM2, RYR1, and the Ca(2+) mobilizing second messenger NAADP (nicotinic acid adenine dinucleotide phosphate). These results indicate that preformed clusters of STIM and ORAI1 enable local Ca(2+) entry events in unstimulated cells. Upon TCR activation, NAADP-evoked Ca(2+) release through RYR1, in coordination with Ca(2+) entry through ORAI1 and STIM, rapidly increases the number of Ca(2+) microdomains, thereby initiating spread of Ca(2+) signals deeper into the cytoplasm to promote full T cell activation. |
