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Research Article Free access | 10.1172/JCI114992

Insulin-like growth factor I gene expression in isolated rat renal collecting duct is stimulated by epidermal growth factor.

S A Rogers, S B Miller, and M R Hammerman

Department of Internal Medicine, Washington University School of Medicine, St. Louis, Missouri 63110.

Find articles by Rogers, S. in: PubMed | Google Scholar

Department of Internal Medicine, Washington University School of Medicine, St. Louis, Missouri 63110.

Find articles by Miller, S. in: PubMed | Google Scholar

Department of Internal Medicine, Washington University School of Medicine, St. Louis, Missouri 63110.

Find articles by Hammerman, M. in: PubMed | Google Scholar

Published January 1, 1991 - More info

Published in Volume 87, Issue 1 on January 1, 1991
J Clin Invest. 1991;87(1):347–351. https://doi.org/10.1172/JCI114992.
© 1991 The American Society for Clinical Investigation
Published January 1, 1991 - Version history
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Abstract

The renal collecting duct is a site of insulin-like growth factor I (IGF I) synthesis. Epidermal growth factor (EGF) is also synthesized within the kidney in the thick ascending limb of Henle's loop and the distal tubule. EGF has been shown to regulate IGF I expression in nonrenal tissues. To shed light upon a role of EGF in intrarenal regulation of IGF I gene expression, plasma membranes prepared from collecting ducts isolated from rat kidney and collecting ducts themselves were incubated in the presence and absence of recombinant human EGF (hEGF). hEGF enhanced phospholipase C activity in collecting duct plasma membranes establishing the potential for EGF signal transduction at this site. Inclusion of hEGF in suspensions of collecting ducts increased production of immunoreactive IGF I in a concentration-dependent manner. Production was stimulated significantly by addition of 10(-8) or 10(-6) M hEGF to suspensions for 2 h. Levels of IGF I mRNA in collecting ducts were increased 2.8-fold after incubation with 10(-6) M hEGF in vitro. Our findings demonstrate a direct action of hEGF to enhance collecting duct IGF I gene expression in vitro. Such enhancement is likely to reflect an effect of EGF to stimulate IGF I production in the collecting duct of the intact kidney. Since EGF is produced in kidney, our findings are consistent with intrarenal paracrine regulation of IGF I gene expression by EGF.

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