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Mosaic variants in genes GNAQ or GNA11 lead to a spectrum of vascular and pigmentary diseases including Sturge-Weber syndrome, in which progressive postnatal neurological deterioration led us to seek biologically targeted therapeutics. Using two cellular models, we find that disease-causing GNAQ/11 variants hyperactivate constitutive and G-protein coupled receptor ligand-induced intracellular calcium signaling in endothelial cells. We go on to show that the aberrant ligand-activated intracellular calcium signal is fueled by extracellular calcium influx through calcium-release-activated channels. Treatment with targeted small interfering RNAs designed to silence the variant allele preferentially corrects both the constitutive and ligand-activated calcium signaling, whereas treatment with a calcium-release-activated channel inhibitor rescues the ligand-activated signal. This work identifies hyperactivated calcium signaling as the primary biological abnormality in GNAQ/11 mosaicism and paves the way for clinical trials with genetic or small molecule therapies.

Original publication

DOI

10.1016/j.jid.2023.08.028

Type

Journal article

Journal

J Invest Dermatol

Publication Date

04/2024

Volume

144

Pages

811 - 819.e4

Keywords

GTP-Binding Protein alpha Subunits, Gq-G11, GTP-Binding Protein alpha Subunits, Mutation, Calcium, Endothelial Cells, Mosaicism, Calcium Signaling, Ligands