Differential localization of prostaglandin E receptor subtypes in human kidney

M. D. Breyer, L. Davis, H. R. Jacobson and R. M. Breyer Department of Pharmacology, Veterans Affairs Medical Center, Nashville, Tennessee 37232-2372, USA. Four prostaglandin E2 (PGE2) receptors designated EP1, EP2, EP3, and EP4 have been pharmacologically identified, cloned, and sequenced. The prese...

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Veröffentlicht in:American journal of physiology. Renal physiology 1996-05, Vol.270 (5), p.912-F918
Hauptverfasser: Breyer, M. D, Davis, L, Jacobson, H. R, Breyer, R. M
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Sprache:eng
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Zusammenfassung:M. D. Breyer, L. Davis, H. R. Jacobson and R. M. Breyer Department of Pharmacology, Veterans Affairs Medical Center, Nashville, Tennessee 37232-2372, USA. Four prostaglandin E2 (PGE2) receptors designated EP1, EP2, EP3, and EP4 have been pharmacologically identified, cloned, and sequenced. The present studies determined the intrarenal distribution of these EP-receptor subtypes in human kidney using in situ hybridization with riboprobes for the human EP receptors. mRNA for the phosphatidylinositol hydrolysis-coupled EP receptor was highly expressed in cortical, outer medullary, and inner medullary collecting duct. RNA for the Gi-coupled EP3 receptor was primarily expressed in the cortical and outer medullary collecting duct, as well as in the medullary thick ascending limb; however, it was absent from the inner medullary collecting duct. Expression of mRNA for EP1 and EP3 in connecting segment could not be excluded. There was no expression of the GS-coupled EP2 receptor mRNA detected in human kidney by in situ hybridization; however, mRNA for the GS-coupled EP4 receptor was highly expressed in the glomerulus. These studies demonstrate distinct regions of intrarenal expression for the different EP receptors and suggest that each receptor subtype may modulate different aspects of renal function in humans.
ISSN:0363-6127
0002-9513
1931-857X
2161-1157
1522-1466
DOI:10.1152/ajprenal.1996.270.5.f912