| Literature DB >> 26490995 |
Bertha C Elias1, Amrita Das2, Diptiben V Parekh1, Glenda Mernaugh1, Rebecca Adams1, Zhufeng Yang2, Cord Brakebusch3, Ambra Pozzi4, Denise K Marciano2, Thomas J Carroll5, Roy Zent6.
Abstract
The Rho GTPase Cdc42 regulates key signaling pathways required for multiple cell functions, including maintenance of shape, polarity, proliferation, migration, differentiation and morphogenesis. Although previous studies have shown that Cdc42 is required for proper epithelial development and maintenance, its exact molecular function in kidney development is not well understood. In this study, we define the specific role of Cdc42 during murine kidney epithelial tubulogenesis by deleting it selectively at the initiation of ureteric bud or metanephric mesenchyme development. Deletion in either lineage results in abnormal tubulogenesis, with profound defects in polarity, lumen formation and the actin cytoskeleton. Ultimately, these defects lead to renal failure. Additionally, in vitro analysis of Cdc42-null collecting duct cells shows that Cdc42 controls these processes by regulating the polarity Par complex (Par3-Par6-aPKC-Cdc42) and the cytoskeletal proteins N-Wasp and ezrin. Thus, we conclude that the principal role of Cdc42 in ureteric bud and metanephric mesenchyme development is to regulate epithelial cell polarity and the actin cytoskeleton.Entities:
Keywords: Epithelial cell; GTPase; Metanephric mesenchyme; Signaling; Ureteric bud
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Year: 2015 PMID: 26490995 PMCID: PMC4712811 DOI: 10.1242/jcs.164509
Source DB: PubMed Journal: J Cell Sci ISSN: 0021-9533 Impact factor: 5.285