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      Mechanical stretch regulates macropinocytosis in Hydra vulgaris

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          Abstract

          Cells rely on a diverse array of engulfment processes to sense, exploit, and adapt to their environments. Among these, macropinocytosis enables indiscriminate and rapid uptake of large volumes of fluid and membrane, rendering it a highly versatile engulfment strategy. Much of the molecular machinery required for macropinocytosis has been well established, yet how this process is regulated in the context of organs and organisms remains poorly understood. Here, we report the discovery of extensive macropinocytosis in the outer epithelium of the cnidarian Hydra vulgaris. Exploiting Hydra’s relatively simple body plan, we developed approaches to visualize macropinocytosis over extended periods of time, revealing constitutive engulfment across the entire body axis. We show that the direct application of planar stretch leads to calcium influx and the inhibition of macropinocytosis. Finally, we establish a role for stretch-activated channels in inhibiting this process. Together, our approaches provide a platform for the mechanistic dissection of constitutive macropinocytosis in physiological contexts and highlight a potential role for macropinocytosis in responding to cell surface tension.

          Abstract

          • Macropinocytosis is a versatile endocytic strategy involved in nutrient acquisition, immune surveillance, and membrane remodeling. Despite extensive molecular characterization, much remains unknown about the regulation of macropinocytosis in tissues.

          • The authors report a previously undescribed form of constitutive macropinocytosis in the epithelium of Hydra and reveal a role for tissue stretch in regulating this process.

          • Our findings suggest that constitutive macropinocytosis may be more pervasive than previously appreciated and highlight a potential role for this biological phenomenon in membrane tensioning and tissue remodeling.

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          Most cited references52

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          Piezo1 and Piezo2 are essential components of distinct mechanically activated cation channels.

          Mechanical stimuli drive many physiological processes, including touch and pain sensation, hearing, and blood pressure regulation. Mechanically activated (MA) cation channel activities have been recorded in many cells, but the responsible molecules have not been identified. We characterized a rapidly adapting MA current in a mouse neuroblastoma cell line. Expression profiling and RNA interference knockdown of candidate genes identified Piezo1 (Fam38A) to be required for MA currents in these cells. Piezo1 and related Piezo2 (Fam38B) are vertebrate multipass transmembrane proteins with homologs in invertebrates, plants, and protozoa. Overexpression of mouse Piezo1 or Piezo2 induced two kinetically distinct MA currents. Piezos are expressed in several tissues, and knockdown of Piezo2 in dorsal root ganglia neurons specifically reduced rapidly adapting MA currents. We propose that Piezos are components of MA cation channels.
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            Computer control of microscopes using µManager.

            With the advent of digital cameras and motorization of mechanical components, computer control of microscopes has become increasingly important. Software for microscope image acquisition should not only be easy to use, but also enable and encourage novel approaches. The open-source software package µManager aims to fulfill those goals. This unit provides step-by-step protocols describing how to get started working with µManager, as well as some starting points for advanced use of the software. © 2010 by John Wiley & Sons, Inc.
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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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                Author and article information

                Contributors
                Role: Monitoring Editor
                Journal
                Mol Biol Cell
                Mol Biol Cell
                molbiolcell
                mboc
                Molecular Biology of the Cell
                The American Society for Cell Biology
                1059-1524
                1939-4586
                01 March 2024
                02 February 2024
                : 35
                : 3
                : br9
                Affiliations
                [a ]Howard Hughes Medical Institute and Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA 94158
                [b ]Department of Zoology and Centre for Molecular Biosciences Innsbruck (CMBI), University of Innsbruck, Technikerstr. 25, A-6020 Innsbruck, Austria
                [c ]Howard Hughes Medical Institute and Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138
                [d ]Howard Hughes Medical Institute Janelia Research Campus, Ashburn, VA, 20147
                King’s College London
                Author notes

                Author Contributions: Investigation, Methodology, Validation, Formal Analysis, Visualization: T.D.S.; Writing – original draft: T.D.S. and K.L.M; Supervision: K.L.M. and R.D.V.; Conceptualization, Writing – review and editing, Funding Acquisition: T.D.S., K.L.M., R.D.V., and B.H..

                Declaration of Interests: The authors declare no competing interests.

                ORCID Id: Taylor D. Skokan, 0000-0002-2494-6672; Kara L. McKinley, 0000-0001-6283-9168; Ronald D. Vale, 0000-0003-3460-2758

                *Address correspondence to: Ronald D. Vale ( valer@ 123456janelia.hhmi.org ); Kara L. McKinley ( kara_mckinley@ 123456harvard.edu ).
                Article
                E22-02-0065
                10.1091/mbc.E22-02-0065
                10916863
                38265917
                371bb3d8-7fcc-455a-ba5a-56ac61d60574
                © 2024 Skokan et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology.

                This article is distributed by The American Society for Cell Biology under license from the author(s). It is available to the public under an Attribution 4.0 International Creative Commons CC-BY 4.0 License.

                History
                : 07 March 2022
                : 12 January 2024
                : 19 January 2024
                Categories
                Brief Reports

                Molecular biology
                Molecular biology

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