| Literature DB >> 28747357 |
Murali K Yanda1, Qiangni Liu1, Liudmila Cebotaru2.
Abstract
Adult-onset autosomal-dominant polycystic kidney disease (ADPKD) is caused by mutations in either the PKD1 or PKD2 gene, leading to malfunction of their gene products, polycystin 1 or 2. Histone deacetylase 6 (HDAC6) expression and activity are increased in PKD1 mutant renal epithelial cells. Here we studied the effect of ACY-1215, a specific HDAC6 inhibitor, on cyst growth in ADPKD. Treatment with ACY-1215 slowed cyst growth in a mouse model of ADPKD that forms massive cysts within 3 wk after knockout of polycystin 1 function. It also prevented cyst formation in MDCK.2 cells, an in vitro model of cystogenesis, and in an ADPKD cell line derived from the proximal tubules from a pkd1-/-.mouse (PN cells). In PN cells ACY-1215 also reduced the size of already established cysts. We found that ACY-1215 lowered cAMP levels and protein expression of adenylyl cyclase 6. Our results suggest that HDAC6 could potentially serve as a therapeutic target in ADPKD.Entities:
Keywords: adenosine 3′,5′-cyclic monophosphate; autosomal-dominant polycystic kidney disease; histone deacetylase 6 inhibitor; polycystic kidney disease; renal cyst growth
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Year: 2017 PMID: 28747357 PMCID: PMC5668593 DOI: 10.1152/ajprenal.00186.2017
Source DB: PubMed Journal: Am J Physiol Renal Physiol ISSN: 1522-1466