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Orai/CRACM1 and K(Ca)3.1 ion channels interact in the human lung mast cell plasma membrane
BACKGROUND: Orai/CRACM1 ion channels provide the major Ca(2+) influx pathway for FcεRI-dependent human lung mast cell (HLMC) mediator release. The Ca(2+)-activated K(+) channel K(Ca)3.1 modulates Ca(2+) influx and the secretory response through hyperpolarisation of the plasma membrane. We hypothesis...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4504158/ https://www.ncbi.nlm.nih.gov/pubmed/26177720 http://dx.doi.org/10.1186/s12964-015-0112-z |
Sumario: | BACKGROUND: Orai/CRACM1 ion channels provide the major Ca(2+) influx pathway for FcεRI-dependent human lung mast cell (HLMC) mediator release. The Ca(2+)-activated K(+) channel K(Ca)3.1 modulates Ca(2+) influx and the secretory response through hyperpolarisation of the plasma membrane. We hypothesised that there is a close functional and spatiotemporal interaction between these Ca(2+)- and K(+)-selective channels. RESULTS: Activation of FcεRI-dependent HLMC K(Ca)3.1 currents was dependent on the presence of extracellular Ca(2+), and attenuated in the presence of the selective Orai blocker GSK-7975A. Currents elicited by the K(Ca)3.1 opener 1-EBIO were also attenuated by GSK-7975A. The Orai1 E106Q dominant-negative mutant ablated 1-EBIO and FcεRI-dependent K(Ca)3.1 currents in HLMCs. Orai1 but not Orai2 was shown to co-immunoprecipitate with K(Ca)3.1 when overexpressed in HEK293 cells, and Orai1 and K(Ca)3.1 were seen to co-localise in the HEK293 plasma membrane using confocal microscopy. CONCLUSION: K(Ca)3.1 activation in HLMCs is highly dependent on Ca(2+) influx through Orai1 channels, mediated via a close spatiotemporal interaction between the two channels. |
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