A Grainyhead-Like 2/Ovo-Like 2 Pathway Regulates Renal Epithelial Barrier Function and Lumen Expansion

被引:60
作者
Aue, Annekatrin [1 ,2 ]
Hinze, Christian [1 ,3 ]
Walentin, Katharina [1 ]
Ruffert, Janett [1 ]
Yurtdas, Yesim [1 ,4 ,7 ]
Werth, Max [1 ]
Chen, Wei [1 ]
Rabien, Anja [4 ,7 ]
Kilic, Ergin [5 ]
Schulzke, Joerg-Dieter [6 ]
Schumann, Michael [6 ]
Schmidt-Ott, Kai M. [1 ,2 ,3 ]
机构
[1] Max Delbruck Ctr Mol Med, D-13125 Berlin, Germany
[2] Charite, Expt & Clin Res Ctr, D-13353 Berlin, Germany
[3] Charite, Dept Nephrol, D-13353 Berlin, Germany
[4] Charite, Dept Urol, D-13353 Berlin, Germany
[5] Charite, Dept Pathol, D-13353 Berlin, Germany
[6] Charite, Dept Gastroenterol, D-13353 Berlin, Germany
[7] Berlin Inst Urol Res, Berlin, Germany
来源
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2015年 / 26卷 / 11期
关键词
TRANSCRIPTION FACTORS; APICAL SURFACE; MESENCHYMAL TRANSITION; SPINDLE ORIENTATION; MOLECULAR NETWORK; TIGHT JUNCTIONS; DROSOPHILA-OVO; ACTIVE GENES; HISTONE H3; E-CADHERIN;
D O I
10.1681/ASN.2014080759
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Grainyhead transcription factors control epithelial barriers, tissue morphogenesis, and differentiation, but their role in the kidney is poorly understood. Here, we report that nephric duct, ureteric bud, and collecting duct epithelia express high levels of grainyhead-like homolog 2 (Grhl2) and that nephric duct lumen expansion is defective in Grhl2-deficient mice. In collecting duct epithelial cells, Grhl2 inactivation impaired epithelial barrier formation and inhibited lumen expansion. Molecular analyses showed that GRHL2 acts as a transcriptional activator and strongly associates with histone H3 lysine 4 trimethylation. Integrating genome-wide GRHL2 binding as well as H3 lysine 4 trimethylation chromatin immunoprecipitation sequencing and gene expression data allowed us to derive a high-confidence GRHL2 target set. GRHL2 transactivated a group of genes including Ovol2, encoding the ovo-like 2 zinc finger transcription factor, as well as E-cadherin, claudin 4 (Cldn4), and the small GTPase Rab25. Ovol2 induction alone was sufficient to bypass the requirement of Grhl2 for E-cadherin, Cldn4, and Rab25 expression. Re-expression of either Ovol2 or a combination of Cldn4 and Rab25 was sufficient to rescue lumen expansion and barrier formation in Grhl2-deficient collecting duct cells. Hence, we identified a Grhl2/Ovol2 network controlling Cldn4 and Rab25 expression that facilitates lumen expansion and barrier formation in subtypes of renal epithelia.
引用
收藏
页码:2704 / 2715
页数:12
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