Similarities and Differences between the Orai1 Variants: Orai1α and Orai1β

Abstract

Orai1, the first identified member of the Orai protein family, is ubiquitously expressed in the animal kingdom. Orai1 was initially characterized as the channel responsible for the store-operated calcium entry (SOCE), a major mechanism that allows cytosolic calcium concentration increments upon receptor-mediated IP3 generation, which results in intracellular Ca2+ store depletion. Furthermore, current evidence supports that abnormal Orai1 expression or function underlies several disorders. Orai1 is, together with STIM1, the key element of SOCE, conducting the Ca2+ release-activated Ca2+ (CRAC) current and, in association with TRPC1, the store-operated Ca2+ (SOC) current. Additionally, Orai1 is involved in non-capacitative pathways, as the arachidonate-regulated or LTC4-regulated Ca2+ channel (ARC/LRC), store-independent Ca2+ influx activated by the secretory pathway Ca2+-ATPase (SPCA2) and the small conductance Ca2+-activated K+ channel 3 (SK3). Furthermore, Orai1 possesses two variants, Orai1α and Orai1β, the latter lacking 63 amino acids in the N-terminus as compared to the full-length Orai1α form, which confers distinct features to each variant. Here, we review the current knowledge about the differences between Orai1α and Orai1β, the implications of the Ca2+ signals triggered by each variant, and their downstream modulatory effect within the cell.

Physiological functions of calcium signaling via Orai1 in cancer

“…Orai1 has two mammalian homologs, Orai2 and Orai3, that form Ca 2+ -selective ion channels to mediate Ca 2+ influx [ 5 ]. Furthermore, Jardin et al described that Orai1 possesses two variants, Orai1α and Orai1β; the latter lacks 63 amino acids in the N-terminus compared to the full-length Orai1α form, and this differences confers distinct features to each variant [ 6 ]. In this review, we focus on the function of Orai1 because among the three types of Orai homologs, most reports have focused on Orai1.…”