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STIM1 is required for attenuation of PMCA‐mediated Ca 2+ clearance during T‐cell activation
Author(s) -
Ritchie Michael F,
Samakai Elsie,
Soboloff Jonathan
Publication year - 2012
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.1038/emboj.2011.495
Subject(s) - biology , attenuation , microbiology and biotechnology , biophysics , physics , optics
T‐cell activation involves a complex signalling cascade uniquely dependent on elevated cytosolic Ca 2+ levels. Further, the spatiotemporal characteristics of this Ca 2+ signal play a critical role in this process via selective activation of transcription factors. In T cells, store‐operated Ca 2+ entry (SOCe) is the primary Ca 2+ influx pathway; however, cytosolic Ca 2+ concentration depends upon the balance between Ca 2+ influx and extrusion. The plasma membrane Ca 2+ ATPase (PMCA) has previously been identified as a critical player in Ca 2+ clearance in T cells. Here, we provide data revealing both functional and physical links between the activation of stromal interacting molecule 1 (STIM1) and PMCA‐mediated Ca 2+ clearance. Due to the ubiquitous expression of both STIM1 and PMCA, these findings have wide‐ranging implications for Ca 2+ signalling in multiple cell types.