Regulation of the renin expression in the retinal pigment epithelium by systemic stimuli

Milenkovic, Vladimir M. and Brockmann, Marisa and Meyer, Christian and Desch, Michael and Schweda, Frank and Kurtz, Armin and Todorov, Vladimir and Strauss, Olaf (2010) Regulation of the renin expression in the retinal pigment epithelium by systemic stimuli. AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 299 (2). F396-F403. ISSN 1931-857X, 1522-1466

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Abstract

Milenkovic VM, Brockmann M, Meyer C, Desch M, Schweda F, Kurtz A, Todorov V, Strauss O. Regulation of the renin expression in the retinal pigment epithelium by systemic stimuli. Am J Physiol Renal Physiol 299: F396-F403, 2010. First published June 2, 2010; doi:10.1152/ajprenal.00576.2009.-The retina expresses a local renin-angiotensin system (RAS). This study aimed to investigate the influence of systemic modulation of renin synthesis on the expression of renin in the retinal pigment epithelium (RPE), which forms part of the blood/retina barrier. Freshly isolated RPE cells showed expression of renin 1A, which is the secreted isoform of renin. Systemic administration of the angiotensin-converting enzyme inhibitor enalapril in mice increased the renin expression in both the kidney and the retina. Systemic infusion of ANG II led to a decrease in the renin expression in the kidney and in the retina and RPE. The ANG II-dependent down-regulation of renin expression in the RPE was prevented by systemic application of the AT(1) receptor blocker losartan. However, water deprivation lead to an increase of the renin expression in the kidney but unexpectedly to a decrease of the renin expression in the retina. In sections of the mouse retina, the ANG II receptor AT(1) was found in the RPE and localized at the blood side of the epithelium. Short-time cultured RPE cells showed increases in intracellular free Ca2+ in response to stimulation by ANG II that were sensitive to losartan. In summary, we conclude that the renin expression in cells of the blood/retina barrier is influenced by the systemic RAS. ANG II circulating in the plasma is likely a mediator of this influence.

Item Type: Article
Uncontrolled Keywords: ANGIOTENSIN-CONVERTING ENZYME; RECEPTOR KNOCKOUT MICE; CAT ELECTRORETINOGRAM; OCULAR-TISSUES; GANGLION-CELLS; BLOOD-PRESSURE; MESSENGER-RNA; BOVINE EYE; SECRETION; KIDNEY; blood barrier; angiotensin; AT(1); water deprivation
Subjects: 500 Science > 570 Life sciences
600 Technology > 610 Medical sciences Medicine
Divisions: Medicine > Lehrstuhl für Augenheilkunde
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: 20 Jul 2020 05:57
Last Modified: 20 Jul 2020 05:57
URI: https://pred.uni-regensburg.de/id/eprint/24339

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