Xestospongins: Potent membrane permeable blockers of the inositol 1,4,5-trisphosphate receptor

被引:525
作者
Gafni, J
Munsch, JA
Lam, TH
Catlin, MC
Costa, LG
Molinski, TF
Pessah, IN
机构
[1] UNIV CALIF DAVIS,SCH VET MED,DEPT MOL BIOSCI,DAVIS,CA 95616
[2] UNIV CALIF DAVIS,GRAD PROGRAM NEUROSCI,DAVIS,CA 95616
[3] UNIV CALIF DAVIS,DEPT CHEM,DAVIS,CA 95616
[4] UNIV WASHINGTON,DEPT ENVIRONM HLTH,SEATTLE,WA 98195
关键词
D O I
10.1016/S0896-6273(00)80384-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Xestospongins (Xe's) A, C, D, araguspongine B, and demethylxestospongin B, a group of macrocyclic bis-1-oxaquinolizidines isolated from the Australian sponge, Xestospongia species, are shown to be potent blockers of IP3-mediated Ca2+ release from endoplasmic reticulum vesicles of rabbit cerebellum. XeC blocks IP3-induced Ca2+ release (IC50 = 358 nM) without interacting with the IP3-binding site, suggesting a mechanism that is independent of the IP3 effector site. Analysis of Pheochormocytoma cells and primary astrocytes loaded with Ca2+-sensitive dye reveals that XeC selectively blocks bradykinin-and carbamylcholine-induced Ca2+ efflux from endoplasmic reticulum stores. Xe's represent a new class of potent, membrane permeable IP3 receptor blockers exhibiting a high selectivity over ryanodine receptors. Xe's are a valuable tool for investigating the structure and function of IP3 receptors and Ca2+ signaling in neuronal and nonneuronal cells.
引用
收藏
页码:723 / 733
页数:11
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