Background: Notch signaling, a conserved mechanism of cell-to-cell communication, plays a crucial role in regulating cellular processes such as proliferation and differentiation in a context-dependent manner. However, the specific contribution of Notch signaling to the progression of polycystic kidney disease (PKD) remains unclear.
Methods: We investigated the changes in Notch signaling activity (Notch1-4) in the kidneys of autosomal dominant PKD (ADPKD) patients and two ADPKD mouse models (early and late onset). Multiple genetic and pharmacologic approaches were used to explore Notch2 signaling during kidney cyst formation in PKD.
Results: Notch2 expression was significantly increased in the kidney tissues of ADPKD patients and mice. Targeted expression of Notch2 intracellular domain (NICD2) in renal epithelial cells resulted in cyst formation and kidney failure in neonatal and adult mice. Mechanistically, Notch2/Hey2 signaling promoted renal epithelial cell proliferation by driving the expression of the ETS homologous factor (Ehf). Depletion of Ehf delayed NICD2 overexpression-induced cyst formation and kidney failure in mice. A gain-of-function mutation in exon 34 of NOTCH2 (c.6426dupT), which caused PKD in patients with Hajdu-Cheney syndrome, accelerated cell growth in cultured human renal epithelial cells by activating HEY2/EHF signaling. Finally, ablation of Notch2 or treatment of a kidney-targeting nanoparticle carrying the liposome (LIPO)/Notch2-siRNA complex, significantly suppressed renal cyst growth in early-onset ADPKD mice.
Conclusions: Notch2 signaling promoted kidney cyst growth, partially by upregulating Ehf expression, and targeting Notch2 might represent a promising therapeutic strategy to control cyst growth in ADPKD.
Copyright © 2025 by the American Society of Nephrology.