Medical Journals

Paracrine Stimulation of Vascular Smooth Muscle Proliferation by Diadenosine Polyphosphates Released from Proximal Tubule Epithelial Cells.

Authors:
  • Jankowski V
  • Karadogan S
  • Vanholder R
  • Nofer J-R
  • Herget-Rosenthal S
  • van der Giet M
  • Tölle M
  • Tran T N A
  • Zidek W
  • Jankowski J

From: Charité, Medizinische Klinik IV (CBF), Berlin, Germany.

Kidney international

  • Publish Date: May 2007
  • ISSN: 0085-2538
  • Volume: 71
  • Issue: 10
  • Pages: 994-1000
  • Medium: Print
  • Language: English
  • Citation (JAMA): Jankowski V, Karadogan S, Vanholder R, et al. Paracrine Stimulation of Vascular Smooth Muscle Proliferation by Diadenosine Polyphosphates Released from Proximal Tubule Epithelial Cells.. Kidney Int. May 2007;71:994-1000

Abstract

The purinergic receptor system plays an important role in the regulation of both vascular and tubular functions within the kidney; however, the release of purinergic agonists other than ATP by renal tissue is not known. In this investigation, we determine if kidney tissue is a source of diadenosine polyphosphates, which have high affinity for the P(2X) and P(2Y) receptors. Both diadenosine pentaphosphate and hexaphosphate were identified by matrix-assisted laser desorption ionization-mass spectrometry in extracts purified from both whole porcine kidney and from cloned cells of the LLC-PK1 cell line. Both polyphosphates in nanomolar concentrations were found to significantly stimulate the proliferation of vascular smooth muscle cells derived from rat thoracic aortas. The purinergic-receptor antagonist, suramin, did not significantly affect the growth-stimulatory properties of the polyphosphates. The growth stimulation of vascular smooth muscle cells by platelet-derived growth factor was potentiated by both diadenosine polyphosphates. We conclude that diadenosine polyphosphates are endogenous purinergic agonists of the kidney that have physiologic and pathophysiologic relevance. These epithelial cell metabolic products have vasoregulatory properties while linking the energy supply and tubular function.

Mesh Headings (Keywords): Animals, Aorta, Thoracic, Cell Proliferation, Cells, Cultured, Dinucleoside Phosphates, Drug Synergism, Epithelial Cells, Kidney Tubules, Proximal, Male, Muscle, Smooth, Vascular, Myocytes, Smooth Muscle, Paracrine Communication, Platelet-Derived Growth Factor, Rats, Rats, Inbred WKY, Rats, Sprague-Dawley, Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization, Swine


Check for Full Text / PubMed Unique Identifier (PMID): 17361116


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

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