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Research Article Free access | 10.1172/JCI114534

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

I Teitelbaum, A Strasheim, and T Berl

Department of Medicine, University of Colorado School of Medicine, Denver 80262.

Find articles by Teitelbaum, I. in: JCI | PubMed | Google Scholar

Department of Medicine, University of Colorado School of Medicine, Denver 80262.

Find articles by Strasheim, A. in: JCI | PubMed | Google Scholar

Department of Medicine, University of Colorado School of Medicine, Denver 80262.

Find articles by Berl, T. in: JCI | PubMed | Google Scholar

Published April 1, 1990 - More info

Published in Volume 85, Issue 4 on April 1, 1990
J Clin Invest. 1990;85(4):1044–1050. https://doi.org/10.1172/JCI114534.
© 1990 The American Society for Clinical Investigation
Published April 1, 1990 - Version history
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Abstract

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.

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