The macula densa prorenin receptor is essential in renin release and blood pressure control

ADM Riquier-Brison, A Sipos… - American Journal …, 2018 - journals.physiology.org
ADM Riquier-Brison, A Sipos, Á Prókai, SL Vargas, lldikó Toma, EJ Meer, KG Villanueva…
American Journal of Physiology-Renal Physiology, 2018journals.physiology.org
The prorenin receptor (PRR) was originally proposed to be a member of the renin-
angiotensin system (RAS); however, recent work questioned their association. The present
paper describes a functional link between the PRR and RAS in the renal juxtaglomerular
apparatus (JGA), a classic anatomical site of the RAS. PRR expression was found in the
sensory cells of the JGA, the macula densa (MD), and immunohistochemistry-localized PRR
to the MD basolateral cell membrane in mouse, rat, and human kidneys. MD cell PRR …
The prorenin receptor (PRR) was originally proposed to be a member of the renin-angiotensin system (RAS); however, recent work questioned their association. The present paper describes a functional link between the PRR and RAS in the renal juxtaglomerular apparatus (JGA), a classic anatomical site of the RAS. PRR expression was found in the sensory cells of the JGA, the macula densa (MD), and immunohistochemistry-localized PRR to the MD basolateral cell membrane in mouse, rat, and human kidneys. MD cell PRR activation led to MAP kinase ERK1/2 signaling and stimulation of PGE2 release, the classic pathway of MD-mediated renin release. Exogenous renin or prorenin added to the in vitro microperfused JGA-induced acute renin release, which was inhibited by removing the MD or by the administration of a PRR decoy peptide. To test the function of MD PRR in vivo, we established a new mouse model with inducible conditional knockout (cKO) of the PRR in MD cells based on neural nitric oxide synthase-driven Cre-lox recombination. Deletion of the MD PRR significantly reduced blood pressure and plasma renin. Challenging the RAS by low-salt diet + captopril treatment caused further significant reductions in blood pressure, renal renin, cyclooxygenase-2, and microsomal PGE synthase expression in cKO vs. wild-type mice. These results suggest that the MD PRR is essential in a novel JGA short-loop feedback mechanism, which is integrated within the classic MD mechanism to control renin synthesis and release and to maintain blood pressure.
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