Saunders R, Nahorski S R, Challiss R A
Department of Cell Physiology and Pharmacology, University of Leicester, UK.
Neuropharmacology. 1998;37(2):273-6. doi: 10.1016/s0028-3908(98)00027-6.
Increasing [Ca2+]e from 1.3 4 mM had little effect on basal phospholipase C activity in baby hamster kidney (BHK) cells stably expressing either type 1alpha metabotropic glutamate (mGlu1alpha) or M3-muscarinic (m3) receptors, but enhanced agonist-stimulated phosphoinositide hydrolysis in BHK-mGlu1alpha, but not BHK-m3 cells, demonstrating that Ca2+(e) selectively modulates phosphoinositide signalling stimulated by this receptor subtype.
将细胞外钙离子浓度([Ca2+]e)从1.3毫摩尔/升提高到4毫摩尔/升,对稳定表达1α型代谢型谷氨酸受体(mGlu1α)或M3型毒蕈碱受体(m3)的叙利亚仓鼠肾(BHK)细胞的基础磷脂酶C活性影响甚微,但增强了激动剂刺激的BHK-mGlu1α细胞中的磷酸肌醇水解,而对BHK-m3细胞无此作用,这表明细胞外钙离子(Ca2+(e))选择性地调节由该受体亚型刺激的磷酸肌醇信号传导。