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• W2020157497 abstract "This perspective addresses two questions: How many store-operated channels (SOCs) are there, and how many mechanisms can account for SOC activation by depleted stores? Accumulating evidence suggests that the SOC family is not limited to the calcium-selective SOC that is responsible for I CRAC (Ca 2+ -SOC), but includes poorly selective cation SOCs (cat-SOCs) that may satisfy physiological needs in diverse excitable and nonexcitable cells. A growing number of studies in different cell types support the idea that all the members of SOC family (Ca 2+ -SOC and cat-SOC) may be activated by depletion of the stores through the same mechanism, which is mediated by calcium influx factor (CIF) and calcium-independent phospholipase A 2 (iPLA 2 ). A conformational coupling model is also discussed. To account for the most recent findings, we propose that two distinct classes of calcium-conducting channels may exist in plasma membrane, which respond to different signals: SOCs, which are activated by depletion of calcium stores through the CIF-iPLA 2 mechanism [no inositol triphosphate (IP 3 ) needed]; and IP 3 receptor–operated channels (IP 3 ROCs), which are activated by IP 3 receptor through a direct coupling mechanism (no store depletion is needed). This model, with two separate mechanisms linked to different channels, may resolve many conflicting findings and interpretations and may give a new perspective on the diversity of calcium influx pathways." @default.
• W2020157497 created "2016-06-24" @default.
• W2020157497 creator A5012643947 @default.
• W2020157497 date "2004-07-27" @default.
• W2020157497 modified "2023-10-16" @default.
• W2020157497 title "Store-Operated Channels: Diversity and Activation Mechanisms" @default.
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• W2020157497 doi "https://doi.org/10.1126/stke.2432004pe34" @default.
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