Key result
Soluble (pro)renin receptor loss reduces acute renal injury, inflammation, and fibrosis after ureteral obstruction.
Why the study?
The soluble (pro)renin receptor (sPRR) has been implicated in blood pressure regulation and kidney disease, motivating an evaluation of whether loss of sPRR confers protection in obstructive kidney disease.
Does genetic loss of the soluble (pro)renin receptor reduce renal tubular injury, inflammation, and fibrosis in mouse models of obstructive kidney disease?
Does genetic loss of the soluble (pro)renin receptor reduce renal tubular injury, inflammation, and fibrosis in mouse models of obstructive kidney disease?
In a preclinical mouse model, preventing soluble (pro)renin receptor formation attenuates acute renal tubular injury, inflammation, and fibrosis during ureteral obstruction, suggesting sPRR may be a therapeutic target in obstructive nephropathy.
Answers are grounded in this paper and cite their sources.
sPRR loss attenuates acute injury markers in obstructed mouse kidneys; leaves open whether targeting sPRR benefits human obstructive nephropathy.
The (pro)renin receptor (PRR) is a multifunctional protein essential for nephron development and renal function. Cleavage of the extracellular domain of the PRR yields a soluble fragment, soluble PRR (sPRR), which has been implicated in blood pressure regulation and kidney disease. In this study, we examined whether loss of sPRR confers protection in obstructive kidney disease. Using CRISPR-Cas9, we developed a mouse with site directed mutagenesis of the PRR cleavage site preventing the formation of sPRR. Male mutant sPRR mice and littermate WTs were subjected to sham surgery, unilateral ureteral obstruction (UUO, 3 days of obstruction), or unilateral ureteral obstruction-release (UUOR, 3 days of obstruction followed by 28 days of recovery). Kidneys were assessed for injury, inflammation, and fibrosis using RT-PCR, Western blot, histology, and functional measures. In the UUO model, WT mice exhibited significant increases in gene expression of tubular injury ( Havcr1), fibrosis ( FN1, Col1a1), and inflammation ( Ccl2) compared to sham WT mice. In contrast, mutant sPRR mice with UUO had reduced expression of Havcr1, FN1, and Ccl2 relative to UUO or sham WT mice. In the UUOR model, WT mice with UUOR displayed elevated expression of Havcr1, Col1a1, Col3a1 and FN1, indicating progressive fibrosis. Mutant sPRR mice showed a trend toward reduced Col13a1 expression and collagen deposition by histology. GFR and BUN were unchanged across groups, consistent with functional compensation by the contralateral kidney. Loss of sPRR reduces tubular injury, inflammation, and fibrosis in UUO with more modest effects in UUOR.
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Sundar et al. (2026) studied Obstructive kidney disease (unilateral ureteral obstruction and obstruction-release models). CRISPR-Cas9 site-directed mutagenesis of the PRR cleavage site (loss of soluble PRR) vs. Wild-type littermate mice (sham or UUO/UUOR) was evaluated on Renal tubular injury (Havcr1), inflammation (Ccl2), and fibrosis (FN1, Col1a1, Col3a1) gene expression and histology. Loss of soluble (pro)renin receptor in male mice reduced renal Havcr1, FN1, and Ccl2 expression after 3-day unilateral ureteral obstruction, with more modest antifibrotic effects after 28-day recovery.
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