| FEBS Letters | |
| Stimulation of G‐protein coupled receptors in vascular smooth muscle cells induces tyrosine kinase dependent increases in calcium without tyrosine phosphorylation of phospholipase C γ‐1 | |
| Raatz Nelson, Stephanie1  Di Salvo, Joseph1  | |
| [1] Department of Physiology, University of Minnesota, 6-255 Millard Hall, 435 Delaware St. SE, Minneapolis, MN 55455, USA | |
| 关键词: Angiotensin-II; Cellular Ca2+; Endothelin; G-protein coupled receptor; Fura-2; Genistein; Phospholipase C; Platelet derived growth factor; Protein tyrosine phosphorylation; Serotonin; Vascular smooth muscle cell; Vasopressin; | |
| DOI : 10.1016/S0014-5793(97)01606-2 | |
| 学科分类:生物化学/生物物理 | |
| 来源: John Wiley & Sons Ltd. | |
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【 摘 要 】
It is often believed that increases in intracellular Ca2+ ([Ca2+]i) resulting from stimulation of G-protein coupled receptors in vascular smooth muscle cells (VSMC) require activation of the β1 isoform of phospholipase C (PLC). However, recent studies showed that rat aortic VSMC do not express PLC β-1 and that stimulation with angiotensin-II induces tyrosine kinase dependent increases in [Ca2+]i and tyrosine phosphorylation of PLC γ-1. Whether this pathway is activated by other vasoactive agents that stimulate G-protein coupled receptors is unknown. Here, we show that A10 VSMC express PLC β-2, PLC β-3, PLC δ-1, and PLC γ-1. The cells also expressed Gαq/11. However, neither PLC β-1 nor PLC β-4 was detected. Stimulation with angiotensin-II, vasopressin, serotonin, or endothelin induced tyrosine kinase dependent increases in [Ca2+]i. However, tyrosine phosphorylation of PLC γ-1 did not occur. In contrast, stimulation with platelet derived growth factor increased [Ca2+]i and tyrosine phosphorylation of PLC γ-1. The results show that tyrosine phosphorylation of PLC γ-1 is not required for tyrosine kinase dependent increases in [Ca2+]i resulting from stimulation of diverse G-protein coupled receptors in VSMC.
【 授权许可】
Unknown
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| RO201912020305480ZK.pdf | 406KB |
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