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A rise in cytosolic Ca2+ is used as a key signalling messenger in eukaryotic cells. The Ca2+ signal drives life and death and controls myriad responses in between. Inherent in the use of such a multifarious signal is the danger of disease, arising from dysregulated Ca2+ signalling. One ancient, highly conserved and widespread Ca2+ entry pathway is the store-operated Ca2+ release-activated Ca2+ (CRAC) channel. Mutations in STIM1 and ORAI1, the genes that encode the functional channel, are tightly linked to a CRAC channelopathy in humans, which encompasses severe combined immune deficiency, myopathy and anhidrotic ectodermal dysplasia. Moreover, sustained Ca2+ entry through the channels leads to a range of systemic disorders, including acute pancreatitis, asthma and inflammatory bowel disease. In this review, we describe how aberrant CRAC channel activity causes a range of diseases, highlighting commonalities between these diverse pathologies.

More information Original publication

DOI

10.1042/BST20253062

Type

Journal article

Publication Date

2025-06-30T00:00:00+00:00

Volume

53

Pages

627 - 642

Total pages

15

Keywords

CRAC channels, calcium signaling, channelopathy, disease, Humans, Calcium Release Activated Calcium Channels, Animals, ORAI1 Protein, Stromal Interaction Molecule 1, Calcium Signaling, Calcium, Mutation, Neoplasm Proteins, Asthma