Cells, Volume 11, Issue 13
2022 July-1 - 145 articles
Cover Story: Serine residues S27 and S30 from the Orai1 channel are PKC substrates. O1wt overexpression without STIM1 inhibits store-operated Ca2+ entry but increases Ca2+ influx and inhibits Ca2+ release in response to ATP and thapsigargin (TG).To study the role of these two phosphorylation sites, we overexpressed O1S27/30A and O1S27/30D. The former increases Ca2+ entry in response to ATP and TG, but it cannot inhibit Ca2+ release as O1wt does, while the latter cannot increase Ca2+ entry but inhibits Ca2+ release, even in the presence of PKC inhibitors. ATP and TG can increase O1DD while decreasing O1AA interaction with the IP3R. O1DD, unlike O1AA, shows a clear intracellular location. O1AA increases while O1DD decreases the frequency of ATP-induced [Ca2+]i oscillations. These data suggest that yje PKC-mediated phosphorylation of the O1 channel inhibits Ca2+ release, facilitating ER Ca2+ refilling. View this paper - Issues are regarded as officially published after their release is announced to the table of contents alert mailing list .
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