TAZ/Wnt-β-catenin/c-MYC axis regulates cystogenesis in polycystic kidney disease.
Eun Ji LeeEunjeong SeoJin Won KimSun Ah NamJong Young LeeJaehee JunSumin OhMinah ParkEek-Hoon JhoKyung Hyun YooJong Hoon ParkYong Kyun KimPublished in: Proceedings of the National Academy of Sciences of the United States of America (2020)
Autosomal-dominant polycystic kidney disease (ADPKD) is the most common genetic renal disease, primarily caused by germline mutation of PKD1 or PKD2, leading to end-stage renal disease. The Hippo signaling pathway regulates organ growth and cell proliferation. Herein, we demonstrate the regulatory mechanism of cystogenesis in ADPKD by transcriptional coactivator with PDZ-binding motif (TAZ), a Hippo signaling effector. TAZ was highly expressed around the renal cyst-lining epithelial cells of Pkd1-deficient mice. Loss of Taz in Pkd1-deficient mice reduced cyst formation. In wild type, TAZ interacted with PKD1, which inactivated β-catenin. In contrast, in PKD1-deficient cells, TAZ interacted with AXIN1, thus increasing β-catenin activity. Interaction of TAZ with AXIN1 in PKD1-deficient cells resulted in nuclear accumulation of TAZ together with β-catenin, which up-regulated c-MYC expression. Our findings suggest that the PKD1-TAZ-Wnt-β-catenin-c-MYC signaling axis plays a critical role in cystogenesis and might be a potential therapeutic target against ADPKD.
Keyphrases
- polycystic kidney disease
- cell proliferation
- epithelial mesenchymal transition
- induced apoptosis
- signaling pathway
- end stage renal disease
- pi k akt
- wild type
- stem cells
- chronic kidney disease
- cell cycle arrest
- peritoneal dialysis
- magnetic resonance
- gene expression
- magnetic resonance imaging
- oxidative stress
- computed tomography
- dendritic cells
- immune response
- long non coding rna
- dna damage
- heat shock protein