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      Wnt9b signaling regulates planar cell polarity and kidney tubule morphogenesis

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          Abstract

          Although many vertebrate organs, such as kidneys, lungs and liver, are composed of epithelial tubules, little is known of the mechanisms that establish the length or diameter of these tubules. In the kidney, defects in the establishment and/or maintenance of tubule diameter are associated with one of the most common inherited human disorders, polycystic kidney disease. Here, we show that attenuation of Wnt9b signaling during kidney morphogenesis affects the planar cell polarity of the epithelium and leads to tubules with significantly increased diameter. Although previous studies showed that polarized cell divisions maintain the diameter of postnatal kidney tubules, we find cell divisions are randomly oriented during embryonic development. Our data suggest that diameter is established during early morphogenetic stages by convergent extension processes and maintained by polarized cell divisions. Wnt9b, signaling through the non-canonical Rho/Jnk branch of the Wnt pathway, is necessary for both of these processes.

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          Most cited references55

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          Autosomal dominant polycystic kidney disease.

          Autosomal dominant polycystic kidney disease is the most prevalent, potentially lethal, monogenic disorder. It is associated with large interfamilial and intrafamilial variability, which can be explained to a large extent by its genetic heterogeneity and modifier genes. An increased understanding of the disorder's underlying genetic, molecular, and cellular mechanisms and a better appreciation of its progression and systemic manifestations have laid out the foundation for the development of clinical trials and potentially effective treatments.
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            Wnt9b plays a central role in the regulation of mesenchymal to epithelial transitions underlying organogenesis of the mammalian urogenital system.

            The vertebrate urogenital system forms due to inductive interactions between the Wolffian duct, its derivative the ureteric bud, and their adjacent mesenchymes. These establish epithelial primordia within the mesonephric (embryonic) and metanephric (adult) kidneys and the Müllerian duct, the anlage of much of the female reproductive tract. We show that Wnt9b is expressed in the inductive epithelia and is essential for the development of mesonephric and metanephric tubules and caudal extension of the Müllerian duct. Wnt9b is required for the earliest inductive response in metanephric mesenchyme. Further, Wnt9b-expressing cells can functionally substitute for the ureteric bud in these interactions. Wnt9b acts upstream of another Wnt, Wnt4, in this process, and our data implicate canonical Wnt signaling as one of the major pathways in the organization of the mammalian urogenital system. Together these findings suggest that Wnt9b is a common organizing signal regulating diverse components of the mammalian urogenital system.
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              Silberblick/Wnt11 mediates convergent extension movements during zebrafish gastrulation.

              Vertebrate gastrulation involves the specification and coordinated movement of large populations of cells that give rise to the ectodermal, mesodermal and endodermal germ layers. Although many of the genes involved in the specification of cell identity during this process have been identified, little is known of the genes that coordinate cell movement. Here we show that the zebrafish silberblick (slb) locus encodes Wnt11 and that Slb/Wnt11 activity is required for cells to undergo correct convergent extension movements during gastrulation. In the absence of Slb/Wnt11 function, abnormal extension of axial tissue results in cyclopia and other midline defects in the head. The requirement for Slb/Wnt11 is cell non-autonomous, and our results indicate that the correct extension of axial tissue is at least partly dependent on medio-lateral cell intercalation in paraxial tissue. We also show that the slb phenotype is rescued by a truncated form of Dishevelled that does not signal through the canonical Wnt pathway, suggesting that, as in flies, Wnt signalling might mediate morphogenetic events through a divergent signal transduction cascade. Our results provide genetic and experimental evidence that Wnt activity in lateral tissues has a crucial role in driving the convergent extension movements underlying vertebrate gastrulation.
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                Author and article information

                Journal
                9216904
                2419
                Nat Genet
                Nature genetics
                1061-4036
                1546-1718
                8 July 2009
                21 June 2009
                July 2009
                1 January 2010
                : 41
                : 7
                : 793-799
                Affiliations
                [1 ]Department of Internal Medicine, Division of Nephrology, University of Texas Southwestern Medical Center, Dallas, TX 75390 USA
                [2 ]Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390 USA
                [3 ]Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, TX 75390 USA
                [4 ]Department of Pathology & Biodefense, Faculty of Medicine, Saga University, Saga, Japan
                [5 ]Department of Molecular, Cell and Developmental Biology & Institute for Cellular and Molecular Biology, University of Texas, Austin, Austin, Texas 78712, USA
                Author notes
                [* ]Author for correspondence: Thomas J. Carroll, Departments of Internal Medicine (Nephrology) and Molecular Biology, University of Texas Southwestern Medical Center, Dallas, 5323 Harry Hines Blvd., Dallas, TX 75390-8856, Tel: 214-648-2680, Thomas.carroll@ 123456utsouthwestern.edu

                Author Contributions

                CMK designed experiments, performed experiments, assembled data and wrote the manuscript, RC performed biochemistry, SA assisted with quantitative analysis on Wnt9b neo/neo kidneys, PI provided KspCre mice and commented on manuscript, JBW assisted with cell orientation analysis, TJC performed initial experiments, designed experiments and wrote manuscript.

                Article
                nihpa119253
                10.1038/ng.400
                2761080
                19543268
                dca777c2-ab05-46e3-8268-d397292559c7
                History
                Funding
                Funded by: National Institute of Diabetes and Digestive and Kidney Diseases : NIDDK
                Award ID: P30 DK074038-01 ||DK
                Categories
                Article

                Genetics
                Genetics

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