학술논문

Cocaine inhibits store-operated Ca2+ entry in brain microvascular endothelial cells: critical role for sigma-1 receptors.
Document Type
Article
Source
Biochemical Journal. 1/1/2016, Vol. 473 Issue 1, p1-5. 5p.
Subject
*SIGMA-1 receptor
*COCAINE
*BRAIN physiology
*CALCIUM channel inhibition
*ENDOTHELIAL cells
*ENDOPLASMIC reticulum
*PHYSIOLOGY
Language
ISSN
0264-6021
Abstract
Sigma-1 receptor (Sig-1R) is an intracellular chaperone protein with many ligands, located at the endoplasmic reticulum (ER). Binding of cocaine to Sig-1R has previously been found to modulate endothelial functions. In the present study, we show that cocaine dramatically inhibits store-operated Ca2+ entry (SOCE), a Ca2+ influx mechanism promoted by depletion of intracellular Ca2+ stores, in rat brain microvascular endothelial cells (RBMVEC). Using either Sig-1R shRNA or pharmacological inhibition with the unrelated Sig-1R antagonists BD-1063 and NE-100, we show that cocaine-induced SOCE inhibition is dependent on Sig-1R. In addition to revealing new insight into fundamental mechanisms of cocaine-induced changes in endothelial function, these studies indicate an unprecedented role for Sig-1R as a SOCE inhibitor. [ABSTRACT FROM AUTHOR]