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Effects of PEP-1-FK506BP on cyst formation in polycystic kidney diseaseopen access

Authors
Jo, Hyo SangEum, Won SikPark, Eun YoungKo, Je YoungKim, Do YeonKim, Dae WonShin, Min JeaSon, OraCho, Su BinPark, Jung HwanLee, Chi HernYeo, Eun JiYeo, Hyeon JiChoi, Yeon JooYoun, Jong KyuCho, Sung-WooPark, JinseuPark, Jong HoonChoi, Soo Young
Issue Date
Sep-2017
Publisher
KOREAN SOCIETY BIOCHEMISTRY & MOLECULAR BIOLOGY
Keywords
Cyst formation; PEP-1-FK506BP; Polycystic kidney diseases; Protein therapy; 3D culture
Citation
BMB REPORTS, v.50, no.9, pp 460 - 465
Pages
6
Journal Title
BMB REPORTS
Volume
50
Number
9
Start Page
460
End Page
465
URI
https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/8161
DOI
10.5483/BMBRep.2017.50.9.090
ISSN
1976-6696
1976-670X
Abstract
Polycystic kidney disease (PKD) is one of the most common inherited disorders, involving progressive cyst formation in the kidney that leads to renal failure. FK506 binding protein 12 (FK506BP) is an immunophilin protein that performs multiple functions, including regulation of cell signaling pathways and survival. In this study, we determined the roles of PEP-1-FK506BP on cell proliferation and cyst formation in PKD cells. Purified PEP-1-FK506BP transduced into PKD cells markedly inhibited cell proliferation. Also, PEP-1-FK506BP drastically inhibited the expression levels of p-Akt, p-p70S6K, p-mTOR, and p-ERK in PKD cells. In a 3D-culture system, PEP-1-FK506BP significantly reduced cyst formation. Furthermore, the combined effects of rapamycin and PEP-1-FK506BP on cyst formation were markedly higher than the effects of individual treatments. These results suggest that PEP-1-FK506BP delayed cyst formation and could be a new therapeutic strategy for renal cyst formation in PKD.
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