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      Local Membrane Curvature Pins and Guides Excitable Membrane Waves in Chemotactic and Macropinocytic Cells - Biomedical Insights From an Innovative Simple Model

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          Abstract

          PIP3 dynamics observed in membranes are responsible for the protruding edge formation in cancer and amoeboid cells. The mechanisms that maintain those PIP3 domains in three-dimensional space remain elusive, due to limitations in observation and analysis techniques. Recently, a strong relation between the cell geometry, the spatial confinement of the membrane, and the excitable signal transduction system has been revealed by Hörning and Shibata (2019) using a novel 3D spatiotemporal analysis methodology that enables the study of membrane signaling on the entire membrane (Hörning and Shibata, 2019). Here, using 3D spatial fluctuation and phase map analysis on actin polymerization inhibited Dictyostelium cells, we reveal a spatial asymmetry of PIP3 signaling on the membrane that is mediated by the contact perimeter of the plasma membrane — the spatial boundary around the cell-substrate adhered area on the plasma membrane. We show that the contact perimeter guides PIP3 waves and acts as a pinning site of PIP3 phase singularities, that is, the center point of spiral waves. The contact perimeter serves as a diffusion influencing boundary that is regulated by a cell size- and shape-dependent curvature. Our findings suggest an underlying mechanism that explains how local curvature can favor actin polymerization when PIP3 domains get pinned at the curved protrusive membrane edges in amoeboid cells.

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          Most cited references61

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          Macropinocytosis of protein is an amino acid supply route in Ras-transformed cells

          Macropinocytosis is a highly conserved endocytic process by which extracellular fluid and its contents are internalized into cells via large, heterogeneous vesicles known as macropinosomes. Oncogenic Ras proteins have been shown to stimulate macropinocytosis but the functional contribution of this uptake mechanism to the transformed phenotype remains unknown 1-3 . Here we show that Ras-transformed cells utilize macropinocytosis to transport extracellular protein into the cell. The internalized protein undergoes proteolytic degradation, yielding amino acids including glutamine that can enter central carbon metabolism. Accordingly, the dependence of Ras-transformed cells on free extracellular glutamine for growth can be suppressed by the macropinocytic uptake of protein. Consistent with macropinocytosis representing an important route of tumor nutrient uptake, its pharmacological inhibition compromised the growth of Ras-transformed pancreatic tumor xenografts. These results identify macropinocytosis as a mechanism by which cancer cells support their unique metabolic needs and point to the possible exploitation of this process in the design of anti-cancer therapies.
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            Mosaic organization of DNA nucleotides

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              Phosphoinositides in cell regulation and membrane dynamics.

              Inositol phospholipids have long been known to have an important regulatory role in cell physiology. The repertoire of cellular processes known to be directly or indirectly controlled by this class of lipids has now dramatically expanded. Through interactions mediated by their headgroups, which can be reversibly phosphorylated to generate seven species, phosphoinositides play a fundamental part in controlling membrane-cytosol interfaces. These lipids mediate acute responses, but also act as constitutive signals that help define organelle identity. Their functions, besides classical signal transduction at the cell surface, include regulation of membrane traffic, the cytoskeleton, nuclear events and the permeability and transport functions of membranes.
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                Author and article information

                Contributors
                Journal
                Front Cell Dev Biol
                Front Cell Dev Biol
                Front. Cell Dev. Biol.
                Frontiers in Cell and Developmental Biology
                Frontiers Media S.A.
                2296-634X
                15 September 2021
                2021
                : 9
                : 670943
                Affiliations
                [1] 1Institute of Biomaterials and Biomolecular Systems, University of Stuttgart , Stuttgart, Germany
                [2] 2Laboratory for Physical Biology, RIKEN Center for Biosystems Dynamics Research , Kobe, Japan
                [3] 3Carl-Ludwig-Institute for Physiology, University of Leipzig , Leipzig, Germany
                Author notes

                Edited by: Robin S. B. Williams, University of London, United Kingdom

                Reviewed by: Robert Roger Kay, Medical Research Council, United Kingdom; Cornelis Weijer, University of Dundee, United Kingdom; Till Bretschneider, University of Warwick, United Kingdom

                *Correspondence: Marcel Hörning marcel.hoerning@ 123456bio.uni-stuttgart.de

                This article was submitted to Molecular and Cellular Pathology, a section of the journal Frontiers in Cell and Developmental Biology

                Article
                10.3389/fcell.2021.670943
                8479871
                0b6c8998-344a-4849-9fdb-2a946b799839
                Copyright © 2021 Hörning, Bullmann and Shibata.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 22 February 2021
                : 16 August 2021
                Page count
                Figures: 7, Tables: 0, Equations: 8, References: 63, Pages: 14, Words: 9302
                Categories
                Cell and Developmental Biology
                Original Research

                dissipative structure,biochemical oscillation,small systems,signal transduction,chemotaxis,pip3,membrane curvature,macropinocytosis

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