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      A Trio-RhoA-Shroom3 pathway is required for apical constriction and epithelial invagination.

      Development (Cambridge, England)
      Animals, Cell Line, Cell Shape, physiology, Chick Embryo, Cryoultramicrotomy, Dogs, Electroporation, Epithelial Cells, metabolism, Fluorescent Antibody Technique, Guanine Nucleotide Exchange Factors, Lens, Crystalline, embryology, Mice, Microfilament Proteins, Morphogenesis, Phosphoproteins, Protein-Serine-Threonine Kinases, Regression Analysis, Signal Transduction, rho GTP-Binding Proteins, rho-Associated Kinases

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          Abstract

          Epithelial invagination is a common feature of embryogenesis. An example of invagination morphogenesis occurs during development of the early eye when the lens placode forms the lens pit. This morphogenesis is accompanied by a columnar-to-conical cell shape change (apical constriction or AC) and is known to be dependent on the cytoskeletal protein Shroom3. Because Shroom3-induced AC can be Rock1/2 dependent, we hypothesized that during lens invagination, RhoA, Rock and a RhoA guanine nucleotide exchange factor (RhoA-GEF) would also be required. In this study, we show that Rock activity is required for lens pit invagination and that RhoA activity is required for Shroom3-induced AC. We demonstrate that RhoA, when activated and targeted apically, is sufficient to induce AC and that RhoA plays a key role in Shroom3 apical localization. Furthermore, we identify Trio as a RhoA-GEF required for Shroom3-dependent AC in MDCK cells and in the lens pit. Collectively, these data indicate that a Trio-RhoA-Shroom3 pathway is required for AC during lens pit invagination.

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