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Research Article Free access | 10.1172/JCI118019

Osmolar regulation of endothelin signaling in rat renal medullary interstitial cells.

M A Vernace, P F Mento, M E Maita, E P Girardi, M D Chang, E P Nord, and B M Wilkes

Department of Medicine, North Shore University Hospital, Manhasset, New York 11030, USA.

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Department of Medicine, North Shore University Hospital, Manhasset, New York 11030, USA.

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Department of Medicine, North Shore University Hospital, Manhasset, New York 11030, USA.

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Department of Medicine, North Shore University Hospital, Manhasset, New York 11030, USA.

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Department of Medicine, North Shore University Hospital, Manhasset, New York 11030, USA.

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Department of Medicine, North Shore University Hospital, Manhasset, New York 11030, USA.

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Department of Medicine, North Shore University Hospital, Manhasset, New York 11030, USA.

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Published July 1, 1995 - More info

Published in Volume 96, Issue 1 on July 1, 1995
J Clin Invest. 1995;96(1):183–191. https://doi.org/10.1172/JCI118019.
© 1995 The American Society for Clinical Investigation
Published July 1, 1995 - Version history
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Abstract

We tested the hypothesis that endothelin (ET) responsiveness in the renal medulla is modulated by ambient osmolarity. Cultured renal medullary interstitial cells (RMICs) were incubated from 3 to 24 h in isosmolar culture medium (300 mOsm/kg H2O) or media rendered hyperosmolar (600 mOsm/kg H2O) by the addition of urea. Under hyperosmolar conditions, the peak of ET-evoked Ca2+ transient was blunted by 45-58% (P < 0.02) and PGE2 accumulation decreased from 16- to 2-fold above basal values (P < 0.001). To explore whether hyperosmolar conditions blunt intracellular signaling via modulation of receptor number or expression, kinetics of ET binding and Northern blot analysis of ETA receptor mRNA was performed. Under hyperosmolar conditions, ETA receptor density was reduced by 84% versus isosmolar conditions (238 +/- 12 vs. 1450 +/- 184 fmol/mg) (P < 0.01). In contrast to the ligand binding studies, ETA receptor mRNA was increased by 58% (P < 0.05) in cells grown under hyperosmolar versus isosmolar media. These observations indicate that in the hyperosmolar setting, ET-evoked intracellular signaling is blunted in RMICs due to ET receptor downregulation. Since ETA receptor mRNA is increased under hyperosmolar conditions, we conclude that ET receptor downregulation is the consequence of either decreased translation of message, increased degradation of receptor peptide, or increased internalization of specific receptor sites.

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