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      Microglial subtypes: diversity within the microglial community

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          Abstract

          Microglia are brain‐resident macrophages forming the first active immune barrier in the central nervous system. They fulfill multiple functions across development and adulthood and under disease conditions. Current understanding revolves around microglia acquiring distinct phenotypes upon exposure to extrinsic cues in their environment. However, emerging evidence suggests that microglia display differences in their functions that are not exclusively driven by their milieu, rather by the unique properties these cells possess. This microglial intrinsic heterogeneity has been largely overlooked, favoring the prevailing view that microglia are a single‐cell type endowed with spectacular plasticity, allowing them to acquire multiple phenotypes and thereby fulfill their numerous functions in health and disease. Here, we review the evidence that microglia might form a community of cells in which each member (or “subtype”) displays intrinsic properties and performs unique functions. Distinctive features and functional implications of several microglial subtypes are considered, across contexts of health and disease. Finally, we suggest that microglial subtype categorization shall be based on function and we propose ways for studying them. Hence, we advocate that plasticity (reaction states) and diversity (subtypes) should both be considered when studying the multitasking microglia.

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          Most cited references90

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          The Microglial Sensome Revealed by Direct RNA Sequencing

          Microglia, the principal neuroimmune sentinels of the brain, continuously sense changes in their environment and respond to invading pathogens, toxins and cellular debris. Microglia exhibit plasticity and can assume neurotoxic or neuroprotective priming states that determine their responses to danger. We used direct RNA sequencing, without amplification or cDNA synthesis, to determine the quantitative transcriptomes of microglia of healthy adult and aged mice. We validated our findings by fluorescent dual in-situ hybridization, unbiased proteomic analysis and quantitative PCR. We report here that microglia have a distinct transcriptomic signature and express a unique cluster of transcripts encoding proteins for sensing endogenous ligands and microbes that we term the “sensome”. With aging, sensome transcripts for endogenous ligand recognition are downregulated, whereas those involved in microbe recognition and host defense are upregulated. In addition, aging is associated with an overall increase in expression of microglial genes involved in neuroprotection.
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            Local self-renewal can sustain CNS microglia maintenance and function throughout adult life.

            Microgliosis is a common response to multiple types of damage in the CNS. However, the origin of the cells involved in this process is still controversial and the relative importance of local expansion versus recruitment of microglia progenitors from the bloodstream is unclear. Here, we investigated the origin of microglia using chimeric animals obtained by parabiosis. We found no evidence of microglia progenitor recruitment from the circulation in denervation or CNS neurodegenerative disease, suggesting that maintenance and local expansion of microglia are solely dependent on the self-renewal of CNS resident cells in these models.
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              Infiltrating monocytes trigger EAE progression, but do not contribute to the resident microglia pool.

              In multiple sclerosis and the experimental autoimmune encephalitis (EAE) mouse model, two pools of morphologically indistinguishable phagocytic cells, microglia and inflammatory macrophages, accrue from proliferating resident precursors and recruitment of blood-borne progenitors, respectively. Whether these cell types are functionally equivalent is hotly debated, but is challenging to address experimentally. Using a combination of parabiosis and myeloablation to replace circulating progenitors without affecting CNS-resident microglia, we found a strong correlation between monocyte infiltration and progression to the paralytic stage of EAE. Inhibition of chemokine receptor-dependent recruitment of monocytes to the CNS blocked EAE progression, suggesting that these infiltrating cells are essential for pathogenesis. Finally, we found that, although microglia can enter the cell cycle and return to quiescence following remission, recruited monocytes vanish, and therefore do not ultimately contribute to the resident microglial pool. In conclusion, we identified two distinct subsets of myelomonocytic cells with distinct roles in neuroinflammation and disease progression.
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                Author and article information

                Contributors
                bertrand.joseph@ki.se
                Journal
                EMBO J
                EMBO J
                10.1002/(ISSN)1460-2075
                EMBJ
                embojnl
                The EMBO Journal
                John Wiley and Sons Inc. (Hoboken )
                0261-4189
                1460-2075
                02 August 2019
                02 September 2019
                02 August 2019
                : 38
                : 17 ( doiID: 10.1002/embj.v38.17 )
                : e101997
                Affiliations
                [ 1 ] Toxicology Unit Institute of Environmental Medicine Karolinska Institutet Stockholm Sweden
                [ 2 ] Departamento de Bioquímica y Biología Molecular Facultad de Farmacia Universidad de Sevilla Sevilla Spain
                [ 3 ] Instituto de Biomedicina de Sevilla‐Hospital Universitario Virgen del Rocío/CSIC/Universidad de Sevilla Sevilla Spain
                [ 4 ] Department of Molecular Medicine Université Laval Quebec QC Canada
                [ 5 ] Axe Neurosciences Centre de Recherche du CHU de Québec‐Université Laval Quebec QC Canada
                Author notes
                [*] [* ]Corresponding author. Tel: +46 703057405; E‐mail: bertrand.joseph@ 123456ki.se
                Author information
                https://orcid.org/0000-0002-9724-6589
                https://orcid.org/0000-0001-5655-9979
                Article
                EMBJ2019101997
                10.15252/embj.2019101997
                6717890
                31373067
                2fa07b07-29f0-4aaa-88da-c7fa46d631ec
                © 2019 The Authors. Published under the terms of the CC BY 4.0 license

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 13 March 2019
                : 29 April 2019
                : 03 May 2019
                Page count
                Figures: 4, Tables: 0, Pages: 18, Words: 15957
                Funding
                Funded by: Barncancerfonden (Swedish Childhood Cancer Foundation)
                Funded by: Cancerfonden (Swedish Cancer Society)
                Funded by: Swedish Cancer Foundation
                Funded by: Hjärnfonden (Swedish Brain Foundation)
                Funded by: Sigrid Juséliuksen Säätiö (Sigrid Jusélius Stiftelse)
                Funded by: Spanish Ministerio de Ciencia, Innovación y Universidades
                Award ID: FEDER/UE RTI2018‐098645‐B‐100
                Funded by: Canada Research Chair (Tier 2) of Neuroimmune Plasticity in Health and Therapy
                Funded by: TracInflam grant from ERA‐NET NEURON Neuroinflammation
                Funded by: Swedish Research Council
                Funded by: Karolinska Institutet Foundation
                Categories
                Review
                Review
                Custom metadata
                2.0
                embj2019101997
                02 September 2019
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.6.8 mode:remove_FC converted:02.09.2019

                Molecular biology
                disease,heterogeneity,homeostasis,microglia,subtypes,immunology,neuroscience
                Molecular biology
                disease, heterogeneity, homeostasis, microglia, subtypes, immunology, neuroscience

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