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      Astrocytes and microglia play orchestrated roles and respect phagocytic territories during neuronal corpse removal in vivo

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          Abstract

          Astrocytes and microglia have specialized roles and display a coordinated response during corpse removal in the live brain.

          Abstract

          Cell death is prevalent throughout life; however, the coordinated interactions and roles of phagocytes during corpse removal in the live brain are poorly understood. We developed photochemical and viral methodologies to induce death in single cells and combined this with intravital optical imaging. This approach allowed us to track multicellular phagocytic interactions with precise spatiotemporal resolution. Astrocytes and microglia engaged with dying neurons in an orchestrated and synchronized fashion. Each glial cell played specialized roles: Astrocyte processes rapidly polarized and engulfed numerous small dendritic apoptotic bodies, while microglia migrated and engulfed the soma and apical dendrites. The relative involvement and phagocytic specialization of each glial cell was plastic and controlled by the receptor tyrosine kinase Mertk. In aging, there was a marked delay in apoptotic cell removal. Thus, a precisely orchestrated response and cross-talk between glial cells during corpse removal may be critical for maintaining brain homeostasis.

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          Most cited references24

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          Programmed cell death in animal development.

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            Autoimmunity and the clearance of dead cells.

            To maintain organismal homeostasis, phagocytes engulf dead cells, which are recognized as dead by virtue of a characteristic "eat me" signal exposed on their surface. The dead cells are then transferred to lysosomes, where their cellular components are degraded for reuse. Inefficient engulfment of dead cells activates the immune system, causing disease such as systemic lupus erythematosus, and if the DNA of the dead cells is not properly degraded, the innate immune response becomes activated, leading to severe anemia and chronic arthritis. Here, we discuss how the endogenous components of dead cells activate the immune system through both extracellular and intracellular pathways. (c) 2010 Elsevier Inc. All rights reserved.
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              Sulforhodamine 101 as a specific marker of astroglia in the neocortex in vivo.

              Glial cells have been identified as key signaling components in the brain; however, methods to investigate their structure and function in vivo have been lacking. Here, we describe a new, highly selective approach for labeling astrocytes in intact rodent neocortex that allows in vivo imaging using two-photon microscopy. The red fluorescent dye sulforhodamine 101 (SR101) was specifically taken up by protoplasmic astrocytes after brief exposure to the brain surface. Specificity was confirmed by immunohistochemistry. In addition, SR101 labeled enhanced green fluorescent protein (EGFP)-expressing astrocytes but not microglial cells in transgenic mice. We used SR101 labeling to quantify morphological characteristics of astrocytes and to visualize their close association with the cortical microvasculature. Furthermore, by combining this method with calcium indicator loading of cell populations, we demonstrated distinct calcium dynamics in astroglial and neuronal networks. We expect SR101 staining to become a principal tool for investigating astroglia in vivo.
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                Author and article information

                Journal
                Sci Adv
                Sci Adv
                SciAdv
                advances
                Science Advances
                American Association for the Advancement of Science
                2375-2548
                June 2020
                26 June 2020
                : 6
                : 26
                : eaba3239
                Affiliations
                [1 ]Department of Neurology, Yale School of Medicine, New Haven, CT, USA.
                [2 ]Department of Neurosurgery, Yale School of Medicine, New Haven, CT, USA.
                [3 ]Department of Biological Sciences, Dartmouth College, Hanover, NH, USA.
                [4 ]Department of Immunobiology, Yale School of Medicine, New Haven, CT, USA.
                [5 ]Department of Pharmacology, Yale School of Medicine, New Haven, CT, USA.
                [6 ]Department of Neuroscience, Yale School of Medicine, New Haven, CT, USA.
                Author notes
                [*]

                These authors contributed equally to this work.

                []Corresponding author. Email: jaime.grutzendler@ 123456yale.edu
                Author information
                http://orcid.org/0000-0001-8854-1335
                http://orcid.org/0000-0001-6080-8712
                http://orcid.org/0000-0002-2596-5154
                http://orcid.org/0000-0001-8883-5739
                http://orcid.org/0000-0002-5693-5572
                http://orcid.org/0000-0001-5990-8708
                http://orcid.org/0000-0002-5000-243X
                Article
                aba3239
                10.1126/sciadv.aba3239
                7319765
                32637606
                02df7557-c1b2-4dbd-b8a6-d9535eb04e29
                Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC).

                This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license, which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.

                History
                : 22 November 2019
                : 12 May 2020
                Funding
                Funded by: doi http://dx.doi.org/10.13039/100000052, NIH Office of the Director;
                Award ID: R01-NS0889734
                Funded by: doi http://dx.doi.org/10.13039/100000052, NIH Office of the Director;
                Award ID: R00-NS099469
                Funded by: doi http://dx.doi.org/10.13039/100000098, NIH Clinical Center;
                Award ID: RF1-AG05825
                Funded by: doi http://dx.doi.org/10.13039/100005351, Neurosurgery Research and Education Foundation;
                Award ID: 14-002715/AANS
                Funded by: NIH-NIAID;
                Award ID: R01-AI089824
                Funded by: NIH-NCI;
                Award ID: R01-CA212376
                Categories
                Research Article
                Research Articles
                SciAdv r-articles
                Cellular Neuroscience
                Neuroscience
                Cellular Neuroscience
                Custom metadata
                Sef Rio

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