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      Adherens junction regulates cryptic lamellipodia formation for epithelial cell migration

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          Abstract

          During the collective migration of epithelial cells, interior cells produce “cryptic” lamellipodia to advance. Ozawa et al. show that formation of cryptic lamellipodia is regulated by WAVE and Arp2/3 complexes that accumulate at the adherens junctions. Without this system, cells lose control of their migration.

          Abstract

          Collective migration of epithelial cells plays crucial roles in various biological processes such as cancer invasion. In migrating epithelial sheets, leader cells form lamellipodia to advance, and follower cells also form similar motile apparatus at cell–cell boundaries, which are called cryptic lamellipodia (c-lamellipodia). Using adenocarcinoma-derived epithelial cells, we investigated how c-lamellipodia form and found that they sporadically grew from around E-cadherin–based adherens junctions (AJs). WAVE and Arp2/3 complexes were localized along the AJs, and silencing them not only interfered with c-lamellipodia formation but also prevented follower cells from trailing the leaders. Disruption of AJs by removing αE-catenin resulted in uncontrolled c-lamellipodia growth, and this was brought about by myosin II activation and the resultant contraction of AJ-associated actomyosin cables. Additional observations indicated that c-lamellipodia tended to grow at mechanically weak sites of the junction. We conclude that AJs not only tie cells together but also support c-lamellipodia formation by recruiting actin regulators, enabling epithelial cells to undergo ordered collective migration.

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          Most cited references70

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          Non-muscle myosin II takes centre stage in cell adhesion and migration.

          Non-muscle myosin II (NM II) is an actin-binding protein that has actin cross-linking and contractile properties and is regulated by the phosphorylation of its light and heavy chains. The three mammalian NM II isoforms have both overlapping and unique properties. Owing to its position downstream of convergent signalling pathways, NM II is central in the control of cell adhesion, cell migration and tissue architecture. Recent insight into the role of NM II in these processes has been gained from loss-of-function and mutant approaches, methods that quantitatively measure actin and adhesion dynamics and the discovery of NM II mutations that cause monogenic diseases.
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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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              Collective cell migration in morphogenesis, regeneration and cancer.

              The collective migration of cells as a cohesive group is a hallmark of the tissue remodelling events that underlie embryonic morphogenesis, wound repair and cancer invasion. In such migration, cells move as sheets, strands, clusters or ducts rather than individually, and use similar actin- and myosin-mediated protrusions and guidance by extrinsic chemotactic and mechanical cues as used by single migratory cells. However, cadherin-based junctions between cells additionally maintain 'supracellular' properties, such as collective polarization, force generation, decision making and, eventually, complex tissue organization. Comparing different types of collective migration at the molecular and cellular level reveals a common mechanistic theme between developmental and cancer research.
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                Author and article information

                Journal
                J Cell Biol
                J Cell Biol
                jcb
                The Journal of Cell Biology
                Rockefeller University Press
                0021-9525
                1540-8140
                05 October 2020
                04 September 2020
                : 219
                : 10
                : e202006196
                Affiliations
                [1 ]Laboratory for Cell Adhesion and Tissue Patterning, RIKEN Center for Biosystems Dynamics Research, Kobe, Japan
                [2 ]Laboratory for Physical Biology, RIKEN Center for Biosystems Dynamics Research, Kobe, Japan
                [3 ]Advanced Bioimaging Center, Department of Molecular & Cell Biology, University of California, Berkeley, Berkeley, CA
                [4 ]Laboratory for Molecular and Cellular Dynamics, RIKEN Center for Biosystems Dynamics Research, Kobe, Japan
                Author notes
                Correspondence to Masatoshi Takeichi: masatoshi.takeichi@ 123456riken.jp
                Author information
                https://orcid.org/0000-0002-9294-9998
                https://orcid.org/0000-0003-3513-9072
                https://orcid.org/0000-0002-9931-3378
                Article
                jcb.202006196
                10.1083/jcb.202006196
                7659716
                32886101
                8c0d4e30-af20-4dbe-ab9c-5747af5042f1
                © 2020 Ozawa et al.

                This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).

                History
                : 30 June 2020
                : 22 July 2020
                : 27 July 2020
                Page count
                Pages: 17
                Funding
                Funded by: RIKEN, DOI http://doi.org/10.13039/501100006264;
                Funded by: Japan Society for the Promotion of Science, DOI http://doi.org/10.13039/501100001691;
                Award ID: 18J01239
                Funded by: Japan Society for the Promotion of Science, DOI http://doi.org/10.13039/501100001691;
                Award ID: LS128
                Funded by: Takeda Science Foundation, DOI http://doi.org/10.13039/100007449;
                Funded by: Uehara Memorial Foundation, DOI http://doi.org/10.13039/100008732;
                Funded by: Japan Society for the Promotion of Science, DOI http://doi.org/10.13039/501100001691;
                Award ID: 20K20379
                Funded by: Japan Science and Technology Agency, DOI http://doi.org/10.13039/501100002241;
                Award ID: JPMJCR1863
                Funded by: Philomathia Foundation;
                Funded by: Chan Zuckerberg Initiative, DOI http://dx.doi.org/10.13039/100014989;
                Award ID: 2019-198142
                Categories
                Article
                Cancer
                Adhesion

                Cell biology
                Cell biology

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