Background: Polycystic kidney disease (PKD) involves renal cysts arising from proliferating tubular cells. Autophagy has been recently suggested as a potential therapeutic target in PKD, and mammalian target of rapamycin (mTOR) is a key negative regulator of autophagy. However, the effect of autophagy regulation on cystogenesis has not been elucidated in PKD mice. Methods: Clinical validation was performed using GEO datasets and autosomal dominant polycystic kidney disease (ADPKD) patient samples. Newly established PKD and LC3 transgenic mice were used for in vivo verifications, and additional tests were performed in vitro and in vivo using multiple autophagy drugs. Findings: Neither autophagy stimulation nor LC3 overexpression alleviated PKD. Furthermore, we observed the inhibitory effect of an autophagy inhibitor on cysts, indicating its possible therapeutic use in a specific group of patients with ADPKD. Interpretation: Our findings provide a novel insight into the pathogenesis related to autophagy in PKD, suggesting that drugs related to autophagy regulation should be considered with caution for treating PKD. Funding Sources: This work was supported by grants from the Bio & Medical Technology Development Program; the Collaborative Genome Program for Fostering New Post-Genome Industry of the NRF; the Basic Science Program.
Bibliographical noteFunding Information:
This work was supported by grants from the Bio & Medical Technology Development Program [2015M3A9B6027555]; the Collaborative Genome Program for Fostering New Post-Genome Industry of the NRF [2014M3C9A2067613]; the Basic Science Program [2016R1A5A1011974 and 2019R1A2B5B03069738]. The funders of the study had no role in the study design, data collection, data analysis, data interpretation, or writing of the report.
All Science Journal Classification (ASJC) codes
- Biochemistry, Genetics and Molecular Biology(all)