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Epidermal growth factor-stimulated phosphoinositide hydrolysis in cultured rat inner medullary collecting tubule cells. Regulation by G protein, calcium, and protein kinase C.

机译:表皮生长因子刺激培养的大鼠内髓收集小管细胞中的磷酸肌醇水解。由G蛋白,钙和蛋白激酶C调控

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摘要

Epidermal growth factor (EGF) exhibits specific saturable binding to cultured rat inner medullary collecting tubule cells and stimulates inositol trisphosphate (IP3) production by these cells in a dose-dependent fashion. EGF-stimulated IP3 production is enhanced by GTP gamma s or AIF4- and is inhibited by GDP beta s or pertussis toxin. Alterations in extracellular Ca2+ have no effect on either basal or EGF-stimulated IP3 production. Similarly, treatment with EGTA which decreases cytosolic Ca2+ is without effect. In contrast, treatment with ionomycin which increases cytosolic Ca2+ has no effect on basal IP3 production but enhances the response to EGF. Activation of protein kinase C inhibits IP3 production in response to either EGF or AIF4-. These studies demonstrate the occurrence of EGF-stimulated phospholipase C activity in the rat inner medullary collecting duct. Stimulation by EGF is transduced by a pertussis toxin-sensitive G protein, unaffected by alterations in extracellular Ca2+, insensitive to a decrement in cytosolic Ca2+, enhanced by an increase in cytosolic Ca2+, and inhibited by protein kinase C.
机译:表皮生长因子(EGF)对培养的大鼠内髓收集小管细胞表现出特定的饱和结合,并以剂量​​依赖的方式刺激这些细胞产生肌醇三磷酸(IP3)。 EGF刺激的IP3的产生被GTPγ或AIF4-增强,被GDPβ或百日咳毒素抑制。细胞外Ca2 +的变化对基础或EGF刺激的IP3产生均无影响。同样,用降低细胞质Ca2 +的EGTA治疗无效。相反,用增加细胞溶质Ca2 +的离子霉素治疗对基础IP3的产生没有影响,但会增强对EGF的反应。蛋白激酶C的激活抑制了对EGF或AIF4-的IP3产生。这些研究证明在大鼠内髓收集管中发生了EGF刺激的磷脂酶C活性。百日咳毒素敏感的G蛋白可转导EGF的刺激,而G蛋白不受细胞外Ca2 +改变的影响,对胞质Ca2 +的减少不敏感,胞质Ca2 +的增加增强,并被蛋白激酶C抑制。

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