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      Systematic elucidation of neuron-astrocyte interaction in models of amyotrophic lateral sclerosis using multi-modal integrated bioinformatics workflow

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      1 , 2 , 14 , 2 , 3 , 1 , 2 , 15 , 4 , 5 , 4 , 6 , 1 , 2 , 16 , 7 , 7 , 17 , 1 , 2 , 8 , 1 , 2 , 18 , 1 , 2 , 19 , 1 , 2 , 8 , 1 , 2 , 1 , 2 , 1 , 2 , 1 , 2 , 20 , 9 , 8 , 7 , 1 , 2 , 2 , 4 , 6 , 10 , 11 , 12 , , 1 , 2 , 13 ,
      Nature Communications
      Nature Publishing Group UK
      Diseases of the nervous system, Amyotrophic lateral sclerosis, Molecular neuroscience, Systems analysis

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          Abstract

          Cell-to-cell communications are critical determinants of pathophysiological phenotypes, but methodologies for their systematic elucidation are lacking. Herein, we propose an approach for the Systematic Elucidation and Assessment of Regulatory Cell-to-cell Interaction Networks (SEARCHIN) to identify ligand-mediated interactions between distinct cellular compartments. To test this approach, we selected a model of amyotrophic lateral sclerosis (ALS), in which astrocytes expressing mutant superoxide dismutase-1 (mutSOD1) kill wild-type motor neurons (MNs) by an unknown mechanism. Our integrative analysis that combines proteomics and regulatory network analysis infers the interaction between astrocyte-released amyloid precursor protein (APP) and death receptor-6 (DR6) on MNs as the top predicted ligand-receptor pair. The inferred deleterious role of APP and DR6 is confirmed in vitro in models of ALS. Moreover, the DR6 knockdown in MNs of transgenic mutSOD1 mice attenuates the ALS-like phenotype. Our results support the usefulness of integrative, systems biology approach to gain insights into complex neurobiological disease processes as in ALS and posit that the proposed methodology is not restricted to this biological context and could be used in a variety of other non-cell-autonomous communication mechanisms.

          Abstract

          Neuron-astrocyte communication plays a key role in pathophysiology, however systematic approaches to unveil it are limited. Here, the authors propose SEARCHIN, a multi-modal integrated workflow, as a tool to identify cross-compartment ligand-receptor interactions, applied to ALS models.

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          Most cited references68

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          Gene Ontology: tool for the unification of biology

          Genomic sequencing has made it clear that a large fraction of the genes specifying the core biological functions are shared by all eukaryotes. Knowledge of the biological role of such shared proteins in one organism can often be transferred to other organisms. The goal of the Gene Ontology Consortium is to produce a dynamic, controlled vocabulary that can be applied to all eukaryotes even as knowledge of gene and protein roles in cells is accumulating and changing. To this end, three independent ontologies accessible on the World-Wide Web (http://www.geneontology.org) are being constructed: biological process, molecular function and cellular component.
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            Neurotoxic reactive astrocytes are induced by activated microglia

            A reactive astrocyte subtype termed A1 is induced after injury or disease of the central nervous system and subsequently promotes the death of neurons and oligodendrocytes.
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              The STRING database in 2017: quality-controlled protein–protein association networks, made broadly accessible

              A system-wide understanding of cellular function requires knowledge of all functional interactions between the expressed proteins. The STRING database aims to collect and integrate this information, by consolidating known and predicted protein–protein association data for a large number of organisms. The associations in STRING include direct (physical) interactions, as well as indirect (functional) interactions, as long as both are specific and biologically meaningful. Apart from collecting and reassessing available experimental data on protein–protein interactions, and importing known pathways and protein complexes from curated databases, interaction predictions are derived from the following sources: (i) systematic co-expression analysis, (ii) detection of shared selective signals across genomes, (iii) automated text-mining of the scientific literature and (iv) computational transfer of interaction knowledge between organisms based on gene orthology. In the latest version 10.5 of STRING, the biggest changes are concerned with data dissemination: the web frontend has been completely redesigned to reduce dependency on outdated browser technologies, and the database can now also be queried from inside the popular Cytoscape software framework. Further improvements include automated background analysis of user inputs for functional enrichments, and streamlined download options. The STRING resource is available online, at http://string-db.org/.
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                Author and article information

                Contributors
                ac2248@cumc.columbia.edu
                sp30@columbia.edu
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                4 November 2020
                4 November 2020
                2020
                : 11
                : 5579
                Affiliations
                [1 ]GRID grid.21729.3f, ISNI 0000000419368729, Departments of Pathology and Cell Biology, , Columbia University, ; New York, NY 10032 USA
                [2 ]GRID grid.21729.3f, ISNI 0000000419368729, Center for Motor Neuron Biology and Diseases, Columbia University, ; New York, NY 10032 USA
                [3 ]GRID grid.21729.3f, ISNI 0000000419368729, Department of Environmental Health Sciences, , Columbia University, ; New York, NY 10032 USA
                [4 ]GRID grid.21729.3f, ISNI 0000000419368729, Department of Systems Biology, , Columbia University, ; New York, NY 10032 USA
                [5 ]DarwinHealth Inc., New York, NY 10032 USA
                [6 ]GRID grid.239585.0, ISNI 0000 0001 2285 2675, Herbert Irving Comprehensive Cancer Center, Columbia University, ; New York, NY USA
                [7 ]GRID grid.239552.a, ISNI 0000 0001 0680 8770, Department of Pediatrics, , Children’s Hospital of Philadelphia Research Institute and the University of Pennsylvania, ; Philadelphia, PA 19104 USA
                [8 ]GRID grid.4708.b, ISNI 0000 0004 1757 2822, Dino Ferrari Center, Department of Pathophysiology and Transplantation, , University of Milan, Neurology Unit, IRCCS Foundation Ca’ Granda Ospedale Maggiore Policlinico, ; Milan, 20122 Italy
                [9 ]GRID grid.418245.e, ISNI 0000 0000 9999 5706, Protein Crystallography Group, Leibniz Institute on Aging – Fritz Lipmann Institute (FLI), ; Beutenbergstr. 11, 07745 Jena, Germany
                [10 ]GRID grid.21729.3f, ISNI 0000000419368729, J.P. Sulzberger Columbia Genome Center, Columbia University, ; New York, NY USA
                [11 ]GRID grid.21729.3f, ISNI 0000000419368729, Department of Biomedical Informatics, , Columbia University, ; New York, NY USA
                [12 ]GRID grid.21729.3f, ISNI 0000000419368729, Department of Biochemistry and Molecular Biophysics, , Columbia University, ; New York, NY USA
                [13 ]GRID grid.21729.3f, ISNI 0000000419368729, Departments of Neurology and Neuroscience, , Columbia University, ; New York, NY 10032 USA
                [14 ]GRID grid.476706.4, Present Address: Spark Therapeutics, ; 3737 Market Street, Philadelphia, PA 19104 USA
                [15 ]GRID grid.410425.6, ISNI 0000 0004 0421 8357, Present Address: Center for Gene Therapy, City of Hope, ; 1500 E. Duarte Road, Duarte, CA 91010 USA
                [16 ]GRID grid.462834.f, Present Address: Institut NeuroMyoGène, CNRS UMR 5310 - INSERM U1217 - Université de Lyon - Université Claude Bernard Lyon 1, ; Lyon, France
                [17 ]GRID grid.16750.35, ISNI 0000 0001 2097 5006, Present Address: Department of Molecular Biology, , Princeton University, ; Princeton, USA
                [18 ]Present Address: Henry Dunant Hospital, BRFAA, Athens, Greece
                [19 ]GRID grid.265073.5, ISNI 0000 0001 1014 9130, Present Address: Department of Neurology and Neurological Science, , Tokyo Medical and Dental University, ; Tokyo, Japan
                [20 ]GRID grid.260917.b, ISNI 0000 0001 0728 151X, Present Address: New York Medical College, ; Valhalla, NY 10595 USA
                Author information
                http://orcid.org/0000-0002-6842-6759
                http://orcid.org/0000-0001-7891-3131
                http://orcid.org/0000-0002-5845-713X
                http://orcid.org/0000-0001-5447-0882
                http://orcid.org/0000-0003-0300-6080
                http://orcid.org/0000-0001-8284-5098
                http://orcid.org/0000-0002-5104-9088
                http://orcid.org/0000-0003-4742-3679
                Article
                19177
                10.1038/s41467-020-19177-y
                7642391
                33149111
                7bedefb7-7cbe-402e-a04f-6e0b27a84f19
                © The Author(s) 2020

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 25 July 2019
                : 2 October 2020
                Funding
                Funded by: European Union’s Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement No 778003
                Funded by: European Union’s Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement No 778003.
                Funded by: FundRef https://doi.org/10.13039/100000005, U.S. Department of Defense (United States Department of Defense);
                Award ID: W81XWH-13-0416
                Award Recipient :
                Funded by: National Institute of Health (NS107442, NS117583, NS111176, AG064596)
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                © The Author(s) 2020

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                diseases of the nervous system,amyotrophic lateral sclerosis,molecular neuroscience,systems analysis

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