Restoration of renal function in zebrafish models of ciliopathies

被引:64
作者
Tobin, Jonathan L. [1 ]
Beales, Philip L. [1 ]
机构
[1] UCL Inst Child Hlth, Mol Med Unit, London WC1N 1EH, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
ciliopathy; kidney cysts; rapamycin; roscovitine; therapeutics;
D O I
10.1007/s00467-008-0898-7
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
The ciliopathies are a class of rare human genetic disease whose aetioligies lie in defective primary cilia. Typical ciliopathies include Bardet-Biedl syndrome (BBS), nephronophthisis (NPHP), Jeune, Joubert, oro-facial-digital (OFD1) and Meckel (MKS) syndromes. All ciliopathies have the common denominator of renal disease, often including tubular cysts. In this study, we have modelled a range of ciliopathies in zebrafish and shown in all cases that knocking down these genes causes cystic lesions in the kidney. We have identified two drugs, rapamycin and roscovitine, which ameliorate the renal phenotype, both morphologically and functionally. This is the first study in which zebrafish has been used to identify potential therapeutic modalities for ciliopathic renal disease, and the results pave the way for further investigations in mammalian models.
引用
收藏
页码:2095 / 2099
页数:5
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