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      Cell-cell contact area affects Notch signaling and Notch-dependent patterning

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          Summary

          During development, cells undergo dramatic changes in their morphology. By affecting contact geometry, these morphological changes could influence cellular communication. However, it has remained unclear whether and how signaling depends on contact geometry. This question is particularly relevant for Notch signaling, which coordinates neighboring cell fates through direct cell-cell signaling. Using micropatterning with a receptor trans-endocytosis assay, we show that signaling between pairs of cells correlates with their contact area. This relationship extends across contact diameters ranging from microns to tens of microns. Mathematical modeling predicts that dependence of signaling on contact area can bias cellular differentiation in Notch-mediated lateral inhibition processes, such that smaller cells are more likely to differentiate into signal-producing cells. Consistent with this prediction, analysis of developing chick inner ear revealed that ligand-producing hair cell precursors have smaller apical footprints than non-hair cells. Together, these results highlight the influence of cell morphology on fate determination processes.

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          Most cited references26

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          Epithelial-mesenchymal transitions in development and pathologies.

          The epithelial-mesenchymal transition (EMT) is a fundamental process governing morphogenesis in multicellular organisms. This process is also reactivated in a variety of diseases including fibrosis and in the progression of carcinoma. The molecular mechanisms of EMT were primarily studied in epithelial cell lines, leading to the discovery of transduction pathways involved in the loss of epithelial cell polarity and the acquisition of a variety of mesenchymal phenotypic traits. Similar mechanisms have also been uncovered in vivo in different species, showing that EMT is controlled by remarkably well-conserved mechanisms. Current studies further emphasise the critical importance of EMT and provide a better molecular and functional definition of mesenchymal cells and how they emerged >500 million years ago as a key event in evolution.
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            Endothelial cells dynamically compete for the tip cell position during angiogenic sprouting.

            Sprouting angiogenesis requires the coordinated behaviour of endothelial cells, regulated by Notch and vascular endothelial growth factor receptor (VEGFR) signalling. Here, we use computational modelling and genetic mosaic sprouting assays in vitro and in vivo to investigate the regulation and dynamics of endothelial cells during tip cell selection. We find that endothelial cells compete for the tip cell position through relative levels of Vegfr1 and Vegfr2, demonstrating a biological role for differential Vegfr regulation in individual endothelial cells. Differential Vegfr levels affect tip selection only in the presence of a functional Notch system by modulating the expression of the ligand Dll4. Time-lapse microscopy imaging of mosaic sprouts identifies dynamic position shuffling of tip and stalk cells in vitro and in vivo, indicating that the VEGFR-Dll4-Notch signalling circuit is constantly re-evaluated as cells meet new neighbours. The regular exchange of the leading tip cell raises novel implications for the concept of guided angiogenic sprouting.
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              Dynamic filopodia transmit intermittent Delta-Notch signaling to drive pattern refinement during lateral inhibition.

              The organization of bristles on the Drosophila notum has long served as a popular model of robust tissue patterning. During this process, membrane-tethered Delta activates intracellular Notch signaling in neighboring epithelial cells, which inhibits Delta expression. This induces lateral inhibition, yielding a pattern in which each Delta-expressing mechanosensory organ precursor cell in the epithelium is surrounded on all sides by cells with active Notch signaling. Here, we show that conventional models of Delta-Notch signaling cannot account for bristle spacing or the gradual refinement of this pattern. Instead, the pattern refinement we observe using live imaging is dependent upon dynamic, basal actin-based filopodia and can be quantitatively reproduced by simulations of lateral inhibition incorporating Delta-Notch signaling by transient filopodial contacts between nonneighboring cells. Significantly, the intermittent signaling induced by these filopodial dynamics generates a type of structured noise that is uniquely suited to the generation of well-ordered, tissue-wide epithelial patterns. (c) 2010 Elsevier Inc. All rights reserved.
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                Author and article information

                Journal
                101120028
                22411
                Dev Cell
                Dev. Cell
                Developmental cell
                1534-5807
                1878-1551
                20 April 2017
                13 March 2017
                17 May 2017
                : 40
                : 5
                : 505-511.e6
                Affiliations
                [1 ]Department of Biochemistry and Molecular Biology, Wise Faculty of Life Science, Tel Aviv University, Tel Aviv 69978, Israel
                [2 ]Department of Medical Genetics, University of Lausanne, Lausanne CH-1015, Switzerland
                [3 ]Swiss Institute of Bioinformatics, Lausanne CH-1015, Switzerland
                [4 ]University College London, Department of Cell and Developmental Biology and Institute for Physics of Living Systems, London WC1E 6BT, UK
                [5 ]The Francis Crick Institute, London NW1 1AT, UK
                [6 ]Sussex Neuroscience, School of Life Sciences, University of Sussex, Falmer, Brighton BN1 9QG, UK
                [7 ]The Biological Design Center and Biomedical Engineering, Boston University, Boston, MA 02215, USA
                [8 ]The Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02115, USA
                Author notes
                [* ]Correspondence: Further information and requests for resources and reagents should be directed to and will be fulfilled by the Lead Contact ,David Sprinzak ( davidsp@ 123456post.tau.ac.il ).
                [9]

                Co-first author

                [10]

                Lead Contact

                Article
                EMS72369
                10.1016/j.devcel.2017.02.009
                5435110
                28292428
                2ec51666-2cee-4d31-bcb9-089acfc34365

                This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/

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                Article

                Developmental biology
                notch signaling,lateral inhibition,cell morphology,live cell imaging,cell-cell contact,inner ear

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