Literature DB >> 11970894

DWnt4 regulates cell movement and focal adhesion kinase during Drosophila ovarian morphogenesis.

E David Cohen1, Marie-Christine Mariol, Rachel M H Wallace, Jason Weyers, Yana G Kamberov, Jacques Pradel, Elizabeth L Wilder.   

Abstract

Cell motility is regulated by extracellular cues and by intracellular factors that accumulate at sites of contact between cells and the extracellular matrix. One of these factors, focal adhesion kinase (FAK), regulates the cycle of focal adhesion formation and disassembly that is required for cell movement to occur. Recently, Wnt signaling has also been implicated in the control of cell movement in vertebrates, but the mechanism through which Wnt proteins influence motility is unclear. We demonstrate that Drosphila Wnt4 is required for cell movement and FAK regulation during ovarian morphogenesis. Dfrizzled2, Disheveled, and protein kinase C are also required. The DWnt4 cell motility pathway is distinct from both the canonical Wnt pathway and the planar polarity pathway. Our data suggest that DWnt4 facilitates motility through regulation of focal adhesions.

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Year:  2002        PMID: 11970894     DOI: 10.1016/s1534-5807(02)00142-9

Source DB:  PubMed          Journal:  Dev Cell        ISSN: 1534-5807            Impact factor:   12.270


  43 in total

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5.  Regulation of Rho and Rac signaling to the actin cytoskeleton by paxillin during Drosophila development.

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7.  Wnt5a mediates nerve growth factor-dependent axonal branching and growth in developing sympathetic neurons.

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8.  The Wnt pathway limits BMP signaling outside of the germline stem cell niche in Drosophila ovaries.

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Journal:  Dev Biol       Date:  2016-06-27       Impact factor: 3.582

9.  Focal adhesion kinase signaling regulates the expression of caveolin 3 and beta1 integrin, genes essential for normal myoblast fusion.

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Journal:  Mol Biol Cell       Date:  2009-05-20       Impact factor: 4.138

10.  Integration of the beta-catenin-dependent Wnt pathway with integrin signaling through the adaptor molecule Grb2.

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Journal:  PLoS One       Date:  2009-11-16       Impact factor: 3.240

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