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1Department of Physiology, Universität Regensburg, Regensburg, Germany; 2National Institutes of Health, Bethesda, Maryland; 3Department of Pediatrics, Faculty of Medicine, University of Regensburg, Regensburg, Germany; and 4University of Virginia, Charlottesville, Virginia
Submitted 30 July 2008 ; accepted in final form 3 March 2009
During metanephric kidney development, renin expression in the renal vasculature begins in larger vessels, shifting to smaller vessels and finally remaining restricted to the terminal portions of afferent arterioles at the entrance into the glomerular capillary network. The mechanisms determining the successive expression of renin along the vascular axis of the kidney are not well understood. Since the cAMP signaling cascade plays a central role in the regulation of both renin secretion and synthesis in the adult kidney, it seemed feasible that this pathway might also be critical for renin expression during kidney development. In the present study we determined the spatiotemporal development of renin expression and the development of the preglomerular arterial tree in mouse kidneys with renin cell-specific deletion of Gs
, a core element for receptor activation of adenylyl cyclases. We found that in the absence of the Gs
protein, renin expression was largely absent in the kidneys at any developmental stage, accompanied by alterations in the development of the preglomerular arterial tree. These data indicate that the maintenance of renin expression following a specific spatiotemporal pattern along the preglomerular vasculature critically depends on the availability of Gs
. We infer from our data that the cAMP signaling pathway is not only critical for the regulation of renin synthesis and secretion in the mature kidney but that it also is critical for establishing the juxtaglomerular expression site of renin during development.
fetal kidney; transgenic mice
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