Roles for Ca2+ Stores Release and Two Ca2+ Influx Pathways in the Fc Epsilon R1-activated Ca2+ Responses of RBL-2H3 Mast Cells
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Molecular Biology
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Cross-linking the high affinity IgE receptor, Fc epsilon R1, with multivalent antigen induces inositol 1,4,5-trisphosphate [Ins(1,4,5)P3]-dependent release of intracellular Ca2+ stores, Ca2+ influx, and secretion of inflammatory mediators from RBL-2H3 mast cells. Here, fluorescence ratio imaging microscopy was used to characterize the antigen-induced Ca2+ responses of single fura-2-loaded RBL-2H3 cells in the presence and absence of extracellular Ca2+ (Ca2+o). As antigen concentration increases toward the optimum for secretion, more cells show a Ca2+ spike or an abrupt increase in [Ca2+]i and the lag time to onset of the response decreases both in the presence and the absence of Ca2+o. When Ca2+o is absent, fewer cells respond to low antigen and the lag times to response are longer than those measured in the presence of Ca2+o, indicating that Ca2+o contributes to Ca2+ stores release. Ins(1,4,5)P3 production is not impaired by the removal of Ca2+o, suggesting that extracellular Ca2+ influences Ca2+ stores release via an effect on the Ins(1,4,5)P3 receptor. Stimulation with low concentrations of antigen can lead, only in the presence of Ca2+o, to a small, gradual increase in [Ca2+]i before the abrupt spike response that indicates store release. We propose that this small, initial [Ca2+]i increase is due to receptor-activated Ca2+ influx that precedes and may facilitate Ca2+ stores release. A mechanism for capacitative Ca2+ entry also exists in RBL-2H3 cells. Our data suggest that a previously undescribed response to Fc epsilon R1 cross-linking, inhibition of Ca2+ stores refilling, may be involved in activating capacitative Ca2+ entry in antigen-stimulated RBL-2H3 cells, thus providing the elevated [Ca2+]i required for optimal secretion. The existence of both capacitative entry and Ca2+ influx that can precede Ca2+ release from intracellular stores suggests that at least two mechanisms of stimulated Ca2+ influx are present in RBL-2H3 cells.
Woo S, James D, Martin T Mol Biol Cell. 2017; 28(6):792-808.
PMID: 28100639 PMC: 5349786. DOI: 10.1091/mbc.E16-08-0617.
Destabilization of TNF-α mRNA by Rapamycin.
Park J, Jeon Y, Lee J, Ahn S, Ha S, Bang S Biomol Ther (Seoul). 2013; 20(1):43-9.
PMID: 24116273 PMC: 3792200. DOI: 10.4062/biomolther.2012.20.1.043.
Single-cell measurements of IgE-mediated FcεRI signaling using an integrated microfluidic platform.
Liu Y, Barua D, Liu P, Wilson B, Oliver J, Hlavacek W PLoS One. 2013; 8(3):e60159.
PMID: 23544131 PMC: 3609784. DOI: 10.1371/journal.pone.0060159.
Ca2+ waves initiate antigen-stimulated Ca2+ responses in mast cells.
Cohen R, Torres A, Ma H, Holowka D, Baird B J Immunol. 2009; 183(10):6478-88.
PMID: 19864608 PMC: 3037335. DOI: 10.4049/jimmunol.0901615.
Small, mobile FcepsilonRI receptor aggregates are signaling competent.
Andrews N, Pfeiffer J, Martinez A, Haaland D, Davis R, Kawakami T Immunity. 2009; 31(3):469-79.
PMID: 19747859 PMC: 2828771. DOI: 10.1016/j.immuni.2009.06.026.