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Am J Physiol Renal Physiol 288: F1032-F1043, 2005. First published January 4, 2005; doi:10.1152/ajprenal.00108.2004
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Expression of NTPDase1 and NTPDase2 in murine kidney: relevance to regulation of P2 receptor signaling

Bellamkonda K. Kishore,1,2,5 Jorge Isaac,3,4 Michel Fausther,6 Sheryl R. Tripp,3,4 Huihui Shi,1,5 Pritmohinder S. Gill,1 Norbert Braun,7 Herbert Zimmermann,7 Jean Sévigny,6 and Simon C. Robson8

Departments of 1Internal Medicine, 2Physiology and 3Pathology, University of Utah Health Sciences Center, and 4Associated Regional University Pathologists Laboratories, Salt Lake City, Utah; 5Nephrology Research, Veterans Affairs Salt Lake City Health Care System, Salt Lake City, Utah; 6Centre de Recherche en Rhumatologie et Immunologie, Université Laval, Sainte-Foy, Québec, Canada; 7Biozentrum der J. W. Goethe-Universität, AK Neurochemie, Zoologisches Institut, Frankfurt am Main, Germany; and 8Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts

Submitted 30 March 2004 ; accepted in final form 30 December 2004

The regulation of renal function by extracellular nucleotides encompasses alterations in glomerular hemodynamics, microvascular function, tubuloglomerular feedback, tubular transport, cell growth or apoptosis, and transport of water and solutes in the medullary collecting duct. Nearly all cells can release ATP or other nucleotides that are then rapidly hydrolyzed in the extracellular milieu. However, little information is available on the cellular expression of ectoenzymes that hydrolyze extracellular nucleotides within the kidney. Nucleoside triphosphate diphosphohydrolases (NTPDases) are plasma membrane-bound ectonucleotidases. NTPDase1 has identity with CD39, a B lymphocyte activation marker, and hydrolyzes extracellular ATP and ADP to AMP within the vasculature, whereas NTPDase2/CD39L(ike)1 preferentially converts ATP to ADP outside of blood vessels. Using immunohistochemical and in situ hybridization approaches, we localized the protein and mRNA of NTPDase1 and 2 in murine renal tissues. In the renal cortex, NTPDase1 is expressed by vascular smooth muscle cells and endothelium in interlobular arteries, afferent glomerular arterioles, and peritubular capillaries. In the inner medulla, NTPDase1 is expressed in ascending thin limbs of Henle's loop, ducts of Bellini, and in the pelvic wall. In contrast, NTPDase2 is expressed in Bowman's capsule, glomerular arterioles, adventitia of blood vessels, and pelvic wall. Thus the distribution patterns of NTPDases have parallels to the known distribution of P2 receptors within the kidney. NTPDases may modulate regulatory effects of ATP and degradation products within the vasculature and other sites and thereby potentially influence physiological as well as multiple pathological events in the kidney.

ectonucleotidases; CD39; ATP; immunohistochemistry; in situ hybridization



Address for reprint requests and other correspondence: B. K. Kishore, Nephrology Research (151M), VA Salt Lake City Health Care System, 500 Foothill Boulevard, Salt Lake City, UT 84148 (E-mail: Bellamkonda.Kishore{at}hsc.utah.edu)




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