IMR Press / FBL / Volume 17 / Issue 3 / DOI: 10.2741/3960

Frontiers in Bioscience-Landmark (FBL) is published by IMR Press from Volume 26 Issue 5 (2021). Previous articles were published by another publisher on a subscription basis, and they are hosted by IMR Press on imrpress.com as a courtesy and upon agreement with Frontiers in Bioscience.

Review
STIM and Orai proteins and the non-capacitative ARC channels
Show Less
1 Department of Pharmacology and Physiology, University of Rochester Medical Center, Rochester, NY
Front. Biosci. (Landmark Ed) 2012, 17(3), 847–860; https://doi.org/10.2741/3960
Published: 1 January 2012
Abstract

The ARC channel is a small conductance, highly Ca²⁺-selective ion channel whose activation is specifically dependent on low concentrations of arachidonic acid acting at an intracellular site. They are widely distributed in diverse cell types where they provide an alternative, store-independent pathway for agonist-activated Ca²⁺ entry. Although biophysically similar to the store-operated CRAC channels, these two conductances function under distinct conditions of agonist stimulation, with the ARC channels providing the predominant route of Ca²⁺ entry during the oscillatory signals generated at low agonist concentrations. Despite these differences in function, like the CRAC channel, activation of the ARC channels is dependent on STIM1, but it is the pool of STIM1 that constitutively resides in the plasma membrane that is responsible. Similarly, both channels are formed by Orai proteins but, whilst the CRAC channel pore is a tetrameric assembly of Orai1 subunits, the ARC channel pore is formed by a heteropentameric assembly of three Orai1 subunits and two Orai3 subunits. There is increasing evidence that the activity of these channels plays a critical role in a variety of different cellular activities.

Keywords
Calcium entry
Calcium signaling
Calcium oscillations
Calcium channels
Arachidonic acid
STIM proteins
Orai proteins
CRAC channels
Beta cells
Review
Share
Back to top