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Regulation of renin release by connexin 43 in As 4.1 cell line

  • Jeong Hee Han
  • , Kyung Ah Kim
  • , Amin Shah
  • , Byung Hyun Park
  • , Woo Hyun Park
  • , Suhn Hee Kim*
  • *Corresponding author for this work
  • Jeonbuk National University

Research output: Contribution to journalJournal articlepeer-review

Abstract

Gap junction channels facilitate chemical and electrical communication between adjacent cells. Gap junction protein, connexin (Cx), is expressed in the endothelial cells of vessels, glomerulus, and renin-secreting cells of the kidney. The purpose of this study was to investigate the role of Cx in renin release using Cx-overexpressing As 4.1 cells. The adenovirus-induced Cx overexpression was conducted by using recombinant adenovirus containing the cDNA encoding Cx37, Cx40, Cx43 (Ad-Cx), and β-galactosidase (Ad-β-gal). In 40-overexpressing cells, basal renin release increased in a time-dependent manner but it was significantly lower than that in Ad-β-gal-treated cells. In Cx37- and Cx43-overexpressing cells, basal renin release was increased in a time-dependent manner, which was not different from control cells. 18-β glycyrrhetinic acid (GA), a gap junction blocker, stimulated renin release dose-dependently and increased intracellular Ca2+ in both Cx43-overexpressing cells and control cells. However, no significant differences were observed. An increase in renin release by 3,4,5-trimethoxybenzoic acid 8-(diethylamino)-octyl ester, a putative antagonist of Ca2+ release from intracellular sequestration sites, was also similar between two groups. These results suggest that Cx43 may unlikely alter the regulation of renin release and intracellular Ca2+ by gap junction blocker in As 4.1 cells.

Original languageEnglish
Pages (from-to)899-902
Number of pages4
JournalPeptides
Volume31
Issue number5
DOIs
StatePublished - 2010.05

Keywords

  • As 4.1 cell line
  • Ca
  • Connexin
  • Gap junction
  • Hormone
  • Renin

Quacquarelli Symonds(QS) Subject Topics

  • Anatomy & Physiology
  • Medicine
  • Biological Sciences

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