The Connexin40 A96S Mutation Causes Renin-Dependent Hypertension

Luebkemeier, Indra and Machura, Katharina and Kurtz, Lisa and Neubauer, Bjoern and Dobrowolski, Radek and Schweda, Frank and Wagner, Charlotte and Willecke, Klaus and Kurtz, Armin (2011) The Connexin40 A96S Mutation Causes Renin-Dependent Hypertension. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 22 (6). pp. 1031-1040. ISSN 1046-6673,

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Abstract

Deletion of the gap-junction-forming protein connexin40 leads to renin-dependent hypertension in mice, but whether observed human variants in connexin40, such as A96S, promote hypertension is unknown. Here, we generated mice with the A96S variant in the mouse connexin40 gene. Although mice homozygous for the A96S mutations had normal expression patterns of connexin40 in the kidney, they were hypertensive, had sixfold higher plasma renin concentrations, and had 40% higher levels of renin mRNA than controls. Renin-expressing cells were aberrantly located outside the media layer of afferent arterioles, and increased renal perfusion pressure did not inhibit renin secretion from kidneys isolated from homozygous A96S mice. Treatment with a low-salt diet in combination with an ACE inhibitor increased renin mRNA levels, plasma renin concentrations, and the number of aberrantly localized renin-producing cells. Taken together, these findings suggest that the A96S mutation in connexin40 leads to renin-dependent hypertension in mice. Modulation of renin secretion by BP critically depends on functional connexin40; with the A96S mutation, the aberrant extravascular localization of renin-secreting cells in the kidney likely impairs the pressure-mediated inhibition of renin secretion.

Item Type: Article
Uncontrolled Keywords: GAP-JUNCTION CHANNELS; CELLS; GENE; ENDOTHELIUM; EXPRESSION; PRESSURE;
Subjects: 500 Science > 570 Life sciences
600 Technology > 610 Medical sciences Medicine
Divisions: Medicine > Lehrstuhl für Innere Medizin II
Biology, Preclinical Medicine > Institut für Physiologie > Prof. Dr. Armin Kurtz
Biology, Preclinical Medicine > Institut für Physiologie > Prof. Dr. Frank Schweda
Depositing User: Dr. Gernot Deinzer
Date Deposited: 09 Jun 2020 10:53
Last Modified: 09 Jun 2020 10:53
URI: https://pred.uni-regensburg.de/id/eprint/20709

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