STIM1 Is a Calcium Sensor Specialized for Digital Signaling

• Published in: Current biology 2009-11, Vol.19 (20), p.1724-1729
• Main Authors: Bird, Gary S., Hwang, Sung-Yong, Smyth, Jeremy T., Fukushima, Miwako, Boyles, Rebecca R., Putney, James W.
• Format: Article
• Language: English
• Subjects: Calcium (intracellular); Calcium - metabolism; Calcium Channels - genetics; Calcium Channels - metabolism; Calcium Signaling; Cell Adhesion Molecules - analysis; Cell Adhesion Molecules - metabolism; Cell Adhesion Molecules - physiology; Cell Line; Endoplasmic Reticulum - metabolism; Humans; Membrane Proteins - analysis; Membrane Proteins - metabolism; Membrane Proteins - physiology; Neoplasm Proteins - analysis; Neoplasm Proteins - metabolism; Neoplasm Proteins - physiology; ORAI1 Protein; SIGNALING; Stromal Interaction Molecule 1; Stromal Interaction Molecule 2
• ISSN: 0960-9822; 1879-0445
• DOI: 10.1016/j.cub.2009.08.022

When cells are activated by calcium-mobilizing agonists at low, physiological concentrations, the resulting calcium signals generally take the form of repetitive regenerative discharges of stored calcium, termed calcium oscillations [1]. These intracellular calcium oscillations have long fascinated biologists as a mode of digitized intracellular signaling. Recent work has highlighted the role of calcium influx as an essential component of calcium oscillations [2]. This influx occurs through a process known as store-operated calcium entry, which is initiated by calcium sensor proteins, STIM1 and STIM2, in the endoplasmic reticulum [3]. STIM2 is activated by changes in endoplasmic reticulum calcium near the resting level, whereas a threshold of calcium depletion is required for STIM1 activation [4]. Here we show that, surprisingly, it is STIM1 and not STIM2 that is exclusively involved in calcium entry during calcium oscillations. The implication is that each oscillation produces a transient drop in endoplasmic reticulum calcium and that this drop is sufficient to transiently activate STIM1. This transient activation of STIM1 can be observed in some cells by total internal reflection fluorescence microscopy. This arrangement nicely provides a clearly defined and unambiguous signaling system, translating a digital calcium release signal into calcium influx that can signal to downstream effectors.