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      Release of VAMP5‐positive extracellular vesicles by retinal Müller glia in vivo

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          Abstract

          Cell‐cell interactions in the central nervous system are based on the release of molecules mediating signal exchange and providing structural and trophic support through vesicular exocytosis and the formation of extracellular vesicles. The specific mechanisms employed by each cell type in the brain are incompletely understood. Here, we explored the means of communication used by Müller cells, a type of radial glial cells in the retina, which forms part of the central nervous system. Using immunohistochemical, electron microscopic, and molecular analyses, we provide evidence for the release of distinct extracellular vesicles from endfeet and microvilli of retinal Müller cells in adult mice in vivo. We identify VAMP5 as a Müller cell‐specific SNARE component that is part of extracellular vesicles and responsive to ischemia, and we reveal differences between the secretomes of immunoaffinity‐purified Müller cells and neurons in vitro. Our findings suggest extracellular vesicle‐based communication as an important mediator of cellular interactions in the retina.

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          Most cited references147

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          Fiji is a distribution of the popular open-source software ImageJ focused on biological-image analysis. Fiji uses modern software engineering practices to combine powerful software libraries with a broad range of scripting languages to enable rapid prototyping of image-processing algorithms. Fiji facilitates the transformation of new algorithms into ImageJ plugins that can be shared with end users through an integrated update system. We propose Fiji as a platform for productive collaboration between computer science and biology research communities.
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            Cutadapt removes adapter sequences from high-throughput sequencing reads

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              HISAT: a fast spliced aligner with low memory requirements.

              HISAT (hierarchical indexing for spliced alignment of transcripts) is a highly efficient system for aligning reads from RNA sequencing experiments. HISAT uses an indexing scheme based on the Burrows-Wheeler transform and the Ferragina-Manzini (FM) index, employing two types of indexes for alignment: a whole-genome FM index to anchor each alignment and numerous local FM indexes for very rapid extensions of these alignments. HISAT's hierarchical index for the human genome contains 48,000 local FM indexes, each representing a genomic region of ∼64,000 bp. Tests on real and simulated data sets showed that HISAT is the fastest system currently available, with equal or better accuracy than any other method. Despite its large number of indexes, HISAT requires only 4.3 gigabytes of memory. HISAT supports genomes of any size, including those larger than 4 billion bases.
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                Author and article information

                Contributors
                fw-pfrieger@gmx.de
                antje.grosche@med.uni-muenchen.de
                Journal
                J Extracell Vesicles
                J Extracell Vesicles
                10.1002/(ISSN)2001-3078
                JEV2
                Journal of Extracellular Vesicles
                John Wiley and Sons Inc. (Hoboken )
                2001-3078
                31 August 2022
                September 2022
                : 11
                : 9 ( doiID: 10.1002/jev2.v11.9 )
                : e12254
                Affiliations
                [ 1 ] Plateforme Imagerie In Vitro, CNRS UAR 3156, Neuropôle University of Strasbourg Strasbourg France
                [ 2 ] Department of Physiological Genomics BioMedical Center BMC Ludwig‐Maximilian University Planegg‐Martinsried Germany
                [ 3 ] Institute of Human Genetics University of Regensburg Regensburg Germany
                [ 4 ] Centre National de la Recherche Scientifique Université de Strasbourg Institut des Neurosciences Cellulaires et Intégratives Strasbourg France
                [ 5 ] Institute for Transfusion Medicine University Hospital Essen University of Duisburg‐Essen Essen Germany
                [ 6 ] Neurology Department Experimental Research in Stroke and Inflammation (ERSI) University Medical Center Hamburg‐Eppendorf Hamburg Germany
                [ 7 ] Metabolomics and Proteomics Core and Research Unit Protein Science Helmholtz‐Zentrum München München Germany
                Author notes
                [*] [* ] Correspondence

                Frank Pfrieger, Plateforme Imagerie In Vitro, CNRS UAR 3156, Neuropôle, University of Strasbourg, Strasbourg 67000, France.

                Email: fw-pfrieger@ 123456gmx.de

                Antje Grosche, Department of Physiological Genomics, BioMedical Center BMC, Ludwig‐Maximilian University, Planegg‐Martinsried 82152, Germany.

                Email: antje.grosche@ 123456med.uni-muenchen.de

                Author information
                https://orcid.org/0000-0003-1328-1115
                https://orcid.org/0000-0002-4927-1851
                https://orcid.org/0000-0003-4336-2768
                https://orcid.org/0000-0002-2255-8393
                https://orcid.org/0000-0003-2446-948X
                https://orcid.org/0000-0002-1630-6827
                https://orcid.org/0000-0001-7085-1431
                https://orcid.org/0000-0003-0338-7530
                Article
                JEV212254
                10.1002/jev2.12254
                9428896
                36043482
                d50e8f07-bb03-43bc-a3f3-273e1078b71a
                © 2022 The Authors. Journal of Extracellular Vesicles published by Wiley Periodicals, LLC on behalf of the International Society for Extracellular Vesicles.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.

                History
                : 25 June 2022
                : 19 April 2022
                : 18 July 2022
                Page count
                Figures: 13, Tables: 0, Pages: 28, Words: 15564
                Funding
                Funded by: Universite de Strasbourg
                Award ID: UPR3212
                Funded by: ProRetina Foundation Germany
                Award ID: Pro‐Re/Seed/Grosche.1‐2014
                Award ID: Pro‐Re/Seed/Kaplan‐Grosche.1‐2019
                Funded by: Centre National de la Recherche Scientifique , doi 10.13039/501100004794;
                Award ID: UPR3212
                Funded by: Deutsche Forschungsgemeinschaft , doi 10.13039/501100001659;
                Award ID: GR 4403/1‐1
                Award ID: GR 4403/5‐1
                Award ID: GR 4403/7‐1
                Award ID: HA 6014/5‐1
                Funded by: Agence Nationale de la Recherche , doi 10.13039/501100001665;
                Award ID: GLIAVAMP
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                September 2022
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.1.7 mode:remove_FC converted:31.08.2022

                neuroglia,exosomes,tetraspanin,gliosis,snare complex,secretome,vitreous body,microvillus

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