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      Interface astrogliosis in contact sport head impacts and military blast exposure

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          Abstract

          Exposure to military blast and repetitive head impacts (RHI) in contact sports is associated with increased risk of long-term neurobehavioral sequelae and cognitive deficits, and the neurodegenerative disease chronic traumatic encephalopathy (CTE). At present, the exact pathogenic mechanisms of RHI and CTE are unknown, and no targeted therapies are available. Astrocytes have recently emerged as key mediators of the multicellular response to head trauma. Here, we investigated interface astrogliosis in blast and impact neurotrauma, specifically in the context of RHI and early stage CTE. We compared postmortem brain tissue from former military veterans with a history of blast exposure with and without a neuropathological diagnosis of CTE, former American football players with a history of RHI with and without a neuropathological diagnosis of CTE, and control donors without a history of blast, RHI exposure or CTE diagnosis. Using quantitative immunofluorescence, we found that astrogliosis was higher at the grey-white matter interface in the dorsolateral frontal cortex, with mixed effects at the subpial surface and underlying cortex, in both blast and RHI donors with and without CTE, compared to controls. These results indicate that certain astrocytic alterations are associated with both impact and blast neurotrauma, and that different astroglial responses take place in distinct brain regions.

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          Most cited references57

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          Astrocytes: biology and pathology

          Astrocytes are specialized glial cells that outnumber neurons by over fivefold. They contiguously tile the entire central nervous system (CNS) and exert many essential complex functions in the healthy CNS. Astrocytes respond to all forms of CNS insults through a process referred to as reactive astrogliosis, which has become a pathological hallmark of CNS structural lesions. Substantial progress has been made recently in determining functions and mechanisms of reactive astrogliosis and in identifying roles of astrocytes in CNS disorders and pathologies. A vast molecular arsenal at the disposal of reactive astrocytes is being defined. Transgenic mouse models are dissecting specific aspects of reactive astrocytosis and glial scar formation in vivo. Astrocyte involvement in specific clinicopathological entities is being defined. It is now clear that reactive astrogliosis is not a simple all-or-none phenomenon but is a finely gradated continuum of changes that occur in context-dependent manners regulated by specific signaling events. These changes range from reversible alterations in gene expression and cell hypertrophy with preservation of cellular domains and tissue structure, to long-lasting scar formation with rearrangement of tissue structure. Increasing evidence points towards the potential of reactive astrogliosis to play either primary or contributing roles in CNS disorders via loss of normal astrocyte functions or gain of abnormal effects. This article reviews (1) astrocyte functions in healthy CNS, (2) mechanisms and functions of reactive astrogliosis and glial scar formation, and (3) ways in which reactive astrocytes may cause or contribute to specific CNS disorders and lesions.
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            Astrocyte-endothelial interactions at the blood-brain barrier.

            The blood-brain barrier, which is formed by the endothelial cells that line cerebral microvessels, has an important role in maintaining a precisely regulated microenvironment for reliable neuronal signalling. At present, there is great interest in the association of brain microvessels, astrocytes and neurons to form functional 'neurovascular units', and recent studies have highlighted the importance of brain endothelial cells in this modular organization. Here, we explore specific interactions between the brain endothelium, astrocytes and neurons that may regulate blood-brain barrier function. An understanding of how these interactions are disturbed in pathological conditions could lead to the development of new protective and restorative therapies.
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              Reactive astrocyte nomenclature, definitions, and future directions

              Reactive astrocytes are astrocytes undergoing morphological, molecular, and functional remodeling in response to injury, disease, or infection of the CNS. Although this remodeling was first described over a century ago, uncertainties and controversies remain regarding the contribution of reactive astrocytes to CNS diseases, repair, and aging. It is also unclear whether fixed categories of reactive astrocytes exist and, if so, how to identify them. We point out the shortcomings of binary divisions of reactive astrocytes into good-vs-bad, neurotoxic-vs-neuroprotective or A1-vs-A2. We advocate, instead, that research on reactive astrocytes include assessment of multiple molecular and functional parameters—preferably in vivo—plus multivariate statistics and determination of impact on pathological hallmarks in relevant models. These guidelines may spur the discovery of astrocyte-based biomarkers as well as astrocyte-targeting therapies that abrogate detrimental actions of reactive astrocytes, potentiate their neuro- and glioprotective actions, and restore or augment their homeostatic, modulatory, and defensive functions.
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                Author and article information

                Contributors
                huberb@bu.edu
                Journal
                Acta Neuropathol Commun
                Acta Neuropathol Commun
                Acta Neuropathologica Communications
                BioMed Central (London )
                2051-5960
                13 April 2022
                13 April 2022
                2022
                : 10
                : 52
                Affiliations
                [1 ]GRID grid.189504.1, ISNI 0000 0004 1936 7558, Department of Anatomy & Neurobiology, , Boston University School of Medicine, ; Boston, MA 02118 USA
                [2 ]GRID grid.410370.1, ISNI 0000 0004 4657 1992, VA Boston Healthcare System, ; 150 S. Huntington Avenue, Boston, MA 02130 USA
                [3 ]GRID grid.189504.1, ISNI 0000 0004 1936 7558, Boston University Alzheimer’s Disease and CTE Centers, , Boston University School of Medicine, ; Boston, MA 02118 USA
                [4 ]GRID grid.189504.1, ISNI 0000 0004 1936 7558, Department of Pathology and Laboratory Medicine, , Boston University School of Medicine, ; Boston, MA 02118 USA
                [5 ]GRID grid.189504.1, ISNI 0000 0004 1936 7558, Department of Neurology, , Boston University School of Medicine, ; Boston, MA 02118 USA
                [6 ]GRID grid.410370.1, ISNI 0000 0004 4657 1992, National Center for PTSD, , VA Boston Healthcare System, ; Boston, MA 02130 USA
                [7 ]VA Bedford Healthcare System, Bedford, MA 01730 USA
                [8 ]GRID grid.189504.1, ISNI 0000 0004 1936 7558, Molecular Aging and Development Laboratory, , Boston University School of Medicine, ; Boston, MA 02118 USA
                [9 ]GRID grid.189504.1, ISNI 0000 0004 1936 7558, Boston University College of Engineering, ; Boston, MA 02115 USA
                Author information
                http://orcid.org/0000-0002-5856-3477
                Article
                1358
                10.1186/s40478-022-01358-z
                9009003
                35418116
                d4308c51-668f-406a-9872-ff5a86766b21
                © The Author(s) 2022

                Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 10 February 2022
                : 29 March 2022
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100000065, National Institute of Neurological Disorders and Stroke;
                Award ID: U54NS115266
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000049, National Institute on Aging;
                Award ID: U19AG068753
                Award ID: P30AG013846
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100000738, U.S. Department of Veterans Affairs;
                Award ID: I01-CX001038
                Award ID: 1IOBX004613
                Award Recipient :
                Categories
                Research
                Custom metadata
                © The Author(s) 2022

                mild traumatic brain injury,repetitive head impacts,blast injury,chronic traumatic encephalopathy,astrogliosis

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