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      Tension at intercellular junctions is necessary for accurate orientation of cell division in the epithelium plane

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          Abstract

          The direction in which a cell divides is set by the orientation of its mitotic spindle and is important for determining cell fate, controlling tissue shape, and maintaining tissue architecture. Divisions parallel to the epithelial plane sustain tissue expansion. By contrast, divisions perpendicular to the plane promote tissue stratification and lead to the loss of epithelial cells from the tissue—an event that has been suggested to promote metastasis. Much is known about the molecular machinery involved in orienting the spindle, but less is known about the contribution of mechanical factors, such as tissue tension, in ensuring spindle orientation in the plane of the epithelium. This is important as epithelia are continuously subjected to mechanical stresses. To explore this further, we subjected suspended epithelial monolayers devoid of extracellular matrix to varying levels of tissue tension to study the orientation of cell divisions relative to the tissue plane. This analysis revealed that lowering tissue tension by compressing epithelial monolayers or by inhibiting myosin contractility increased the frequency of out-of-plane divisions. Reciprocally, increasing tissue tension by elevating cell contractility or by tissue stretching restored accurate in-plane cell divisions. Moreover, a characterization of the geometry of cells within these epithelia suggested that spindles can sense tissue tension through its impact on tension at subcellular surfaces, independently of their shape. Overall, these data suggest that accurate spindle orientation in the plane of the epithelium relies on a threshold level of tension at intercellular junctions.

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          Most cited references53

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          Adherens junctions: from molecules to morphogenesis.

          How adhesive interactions between cells generate and maintain animal tissue structure remains one of the most challenging and long-standing questions in cell and developmental biology. Adherens junctions (AJs) and the cadherin-catenin complexes at their core are therefore the subjects of intense research. Recent work has greatly advanced our understanding of the molecular organization of AJs and how cadherin-catenin complexes engage actin, microtubules and the endocytic machinery. As a result, we have gained important insights into the molecular mechanisms of tissue morphogenesis.
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            Mechanical stretch triggers rapid epithelial cell division through Piezo1

            Despite acting as a barrier for the organs they encase, epithelial cells turnover at some of the fastest rates in the body. Yet, epithelial cell division must be tightly linked to cell death to preserve barrier function and prevent tumour formation. How do the number of dying cells match those dividing to maintain constant numbers? We previously found that when epithelial cells become too crowded, they activate the stretch-activated channel Piezo1 to trigger extrusion of cells that later die 1 . Conversely, what controls epithelial cell division to balance cell death at steady state? Here, we find that cell division occurs in regions of low cell density, where epithelial cells are stretched. By experimentally stretching epithelia, we find that mechanical stretch itself rapidly stimulates cell division through activation of the same Piezo1 channel. To do so, stretch triggers cells paused in early G2 to activate calcium-dependent ERK1/2 phosphorylation that activates cyclin B transcription necessary to drive cells into mitosis. Although both epithelial cell division and cell extrusion require Piezo1 at steady state, the type of mechanical force controls the outcome: stretch induces cell division whereas crowding induces extrusion. How Piezo1-dependent calcium transients activate two opposing processes may depend on where and how Piezo1 is activated since it accumulates in different subcellular sites with increasing cell density. In sparse epithelial regions where cells divide, Piezo1 localizes to the plasma membrane and cytoplasm whereas in dense regions where cells extrude, it forms large cytoplasmic aggregates. Because Piezo1 senses both mechanical crowding and stretch, it may act as a homeostatic sensor to control epithelial cell numbers, triggering extrusion/apoptosis in crowded regions and cell division in sparse regions.
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              Hydrostatic pressure and the actomyosin cortex drive mitotic cell rounding.

              During mitosis, adherent animal cells undergo a drastic shape change, from essentially flat to round. Mitotic cell rounding is thought to facilitate organization within the mitotic cell and be necessary for the geometric requirements of division. However, the forces that drive this shape change remain poorly understood in the presence of external impediments, such as a tissue environment. Here we use cantilevers to track cell rounding force and volume. We show that cells have an outward rounding force, which increases as cells enter mitosis. We find that this mitotic rounding force depends both on the actomyosin cytoskeleton and the cells' ability to regulate osmolarity. The rounding force itself is generated by an osmotic pressure. However, the actomyosin cortex is required to maintain this rounding force against external impediments. Instantaneous disruption of the actomyosin cortex leads to volume increase, and stimulation of actomyosin contraction leads to volume decrease. These results show that in cells, osmotic pressure is balanced by inwardly directed actomyosin cortex contraction. Thus, by locally modulating actomyosin-cortex-dependent surface tension and globally regulating osmotic pressure, cells can control their volume, shape and mechanical properties.
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                Author and article information

                Journal
                7505876
                Proc Natl Acad Sci U S A
                Proc Natl Acad Sci U S A
                Proceedings of the National Academy of Sciences of the United States of America
                0027-8424
                1091-6490
                06 December 2022
                01 December 2022
                17 January 2023
                23 January 2023
                : 119
                : 49
                : e2201600119
                Affiliations
                [a ]London Centre for Nanotechnology, University College London, London WC1H 0AH, UK
                [b ]Department of Civil and Environmental Engineering, Politecnico di Milano, Milano 20133, Italy
                [c ]Medical Research Council (MRC)-Laboratory for Molecular Cell Biology, University College London, London WC1E 6BT, UK
                [d ]Medical Research Council (MRC)-Laboratory of Molecular Biology, Cambridge CB2 0QH, UK
                [e ]Department of Engineering, University of Cambridge, Cambridge CB2 1PZ, UK
                [f ]Institute for the Physics of Living Systems, University College London, London WC1E 6BT, UK
                [g ]Department of Cell and Developmental Biology, University College London, London WC1E 6AR, UK
                Author notes
                [3 ]To whom correspondence may be addressed. g.charras@ 123456ucl.ac.uk .
                [1]

                Present address: Laboratoire de Biologie du Développement, Institut Biologie Paris Seine, UMR 7622 CNRS-Sorbonne Université, INSERM ERL U1156, Paris 75005, France.

                [2]

                Present address: Altos Labs Cambridge Institute, Cambridge, CB21 6GP, UK.

                Edited by Matthieu Piel, Institut Curie, Paris Cedex 05, France; by Editorial Board Member Rebecca Heald

                Author information
                https://orcid.org/0000-0002-9976-462X
                https://orcid.org/0000-0001-7829-8757
                https://orcid.org/0000-0003-2805-5313
                https://orcid.org/0000-0002-6656-9430
                https://orcid.org/0000-0002-0280-3531
                https://orcid.org/0000-0002-7902-0279
                Article
                EMS160153
                10.1073/pnas.2201600119
                7614093
                36454762
                2b6c9013-6b84-4c0d-9033-70caefb2fc42

                This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND).

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                Categories
                Article

                spindle orientation,tissue tension,out-of-plane division,epithelium

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