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      Cytonemes are required for the establishment of a normal Hedgehog morphogen gradient in Drosophila epithelia

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          Summary

          Hedgehog (Hh) signalling is important in development, stem cell biology and disease. In a variety of tissues, Hh acts as a morphogen to regulate growth and cell fate specification. Several hypotheses have been proposed to explain morphogen movement, one of which is transport via filopodia-like protrusions called cytonemes. Here, we analyse the mechanism underlying Hh movement in the wing disc and the abdominal epidermis of Drosophila. We show that, in both epithelia, cells generate cytonemes in regions of Hh signalling. These protrusions are actin-based and span several cell diameters. Various Hh signalling components localise to cytonemes, as well as to punctate structures that move along cytonemes and are probably exovesicles. Using in vivo imaging, we show that cytonemes are dynamic structures and that Hh gradient establishment correlates with cytoneme formation in space and time. Indeed, mutant conditions that affect cytoneme formation reduce both cytoneme length and Hh gradient length. Our results suggest that cytoneme-mediated Hh transport is the mechanistic basis for Hh gradient formation.

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          Most cited references65

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          R: A Language and Environment for Statistical Computing.

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            Planar polarized actomyosin contractile flows control epithelial junction remodelling.

            Force generation by Myosin-II motors on actin filaments drives cell and tissue morphogenesis. In epithelia, contractile forces are resisted at apical junctions by adhesive forces dependent on E-cadherin, which also transmits tension. During Drosophila embryonic germband extension, tissue elongation is driven by cell intercalation, which requires an irreversible and planar polarized remodelling of epithelial cell junctions. We investigate how cell deformations emerge from the interplay between force generation and cortical force transmission during this remodelling in Drosophila melanogaster. The shrinkage of dorsal-ventral-oriented ('vertical') junctions during this process is known to require planar polarized junctional contractility by Myosin II (refs 4, 5, 7, 12). Here we show that this shrinkage is not produced by junctional Myosin II itself, but by the polarized flow of medial actomyosin pulses towards 'vertical' junctions. This anisotropic flow is oriented by the planar polarized distribution of E-cadherin complexes, in that medial Myosin II flows towards 'vertical' junctions, which have relatively less E-cadherin than transverse junctions. Our evidence suggests that the medial flow pattern reflects equilibrium properties of force transmission and coupling to E-cadherin by α-Catenin. Thus, epithelial morphogenesis is not properly reflected by Myosin II steady state distribution but by polarized contractile actomyosin flows that emerge from interactions between E-cadherin and actomyosin networks.
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              The many faces of actin: matching assembly factors with cellular structures.

              Actin filaments are major components of at least 15 distinct structures in metazoan cells. These filaments assemble from a common pool of actin monomers, but do so at different times and places, and in response to different stimuli. All of these structures require actin-filament assembly factors. To date, many assembly factors have been identified, including Arp2/3 complex, multiple formin isoforms and spire. Now, a major task is to figure out which factors assemble which actin-based structures. Here, we focus on structures at the plasma membrane, including both sheet-like protrusive structures (such as lamellipodia and ruffles) and finger-like protrusions (such as filopodia and microvilli). Insights gained from studies of adherens junctions and the immunological synapse are also considered.
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                Author and article information

                Journal
                100890575
                21417
                Nat Cell Biol
                Nat. Cell Biol.
                Nature cell biology
                1465-7392
                1476-4679
                25 October 2013
                13 October 2013
                November 2013
                01 May 2014
                : 15
                : 11
                : 10.1038/ncb2856
                Affiliations
                [1 ]Centro de Biología Molecular “Severo Ochoa” (CSIC-UAM), Nicolas Cabrera 1, Universidad Autónoma de Madrid, Cantoblanco, E-28049 Madrid, Spain.
                [2 ]Department of Zoology, University of Cambridge, Downing Street, Cambridge, CB2 3EJ, UK
                Author notes

                AUTHOR CONTRIBUTIONS: MB designed and performed experiments, analysed data and wrote the paper; ACG performed experiments and analysed data; IS and LGM performed experiments; GA designed and performed experiments and analysed data; CRN generated constructs for Flo2 overexpression and helped with RNAi screening and generating mutant clones; IG designed and performed experiments, analysed data and wrote the paper.

                [3]

                Current address: Biomedical Sciences Research Complex, University of St Andrews, North Haugh, St Andrews, KY16 9ST, UK

                [4 ]Corresponding authors: Iguerrero@ 123456cbm.uam.es Phone: Office: +34 91 196 4680. Lab: +34 91 196 4465. mb273@ 123456st-andrews.ac.uk Phone: +44 1334 467199.
                Article
                EMS54668
                10.1038/ncb2856
                3840581
                24121526
                16d15fb2-8645-4caf-a8f9-ef6e45d76fca

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                Cell biology
                Cell biology

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