Abstract

The molecular nature of store-operated Ca(2+)-selective channels has remained an enigma, due largely to the continued inability to convincingly demonstrate Ca(2+)-selective store-operated currents resulting from exogenous expression of known genes. Recent findings have implicated two proteins, Stim1 and Orai1, as having essential roles in store-operated Ca(2+) entry across the plasma membrane. However, transient overexpression of these proteins on their own results in little or no increase in store-operated entry. Here we demonstrate dramatic synergism between these two mediators; co-transfection of HEK293 cells with Stim1 and Orai1 results in an approximate 20-fold increase in store-operated Ca(2+) entry and Ca(2+)-selective current. This demonstrates that these two proteins are limiting for both the signaling and permeation mechanisms for Ca(2+)-selective store-operated Ca(2+) entry. There are three mammalian homologs of Orai1, and in expression experiments they all produced or augmented store-operated Ca(2+) entry with efficacies in the order Orai1 > Orai2 > Orai3. Stim1 apparently initiates the signaling process by acting as a Ca(2+) sensor in the endoplasmic reticulum. This results in rearrangement of Stim1 within the cell and migration toward the plasma membrane to regulate in some manner Orai1 located in the plasma membrane. However, we demonstrate that Stim1 does not incorporate in the surface membrane, and thus likely regulates or interacts with Orai1 at sites of close apposition between the plasma membrane and an intracellular Stim1-containing organelle.

Highlights

  • Store-operated Ca2ϩ (SOC)3 influx is the major mechanism for Ca2ϩ entry in many non-excitable cell types

  • SOC entry was assessed by examining the magnitude of the [Ca2ϩ]i signal upon reintroduction of Ca2ϩ to cells previously treated with the sarcoplasmic-endoplasmic reticulum

  • By use of total internal reflected fluorescence (TIRF) microscopy with HEK293 cells transfected with EYFP-Stim1, we confirmed the observation made by Zhang et al [5] and by Liou et al [2] that Stim1 does move to the vicinity of the plasma membrane following depletion of Ca2ϩ stores with thapsigargin (Fig. 6A)

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Summary

Introduction

Store-operated Ca2ϩ (SOC)3 influx is the major mechanism for Ca2ϩ entry in many non-excitable cell types. The IV relationships for the to, and is incorporated into the plasma membrane where it Orai2 ϩ Stim1 currents showed strong inward rectification, interacts with key players in the store-operated Ca2ϩ entry typical of Icrac-like currents (Fig. 4C).

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