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      Mechanosensory Signaling in Astrocytes

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          Abstract

          Mechanosensitivity is a well-known feature of astrocytes, however, its underlying mechanisms and functional significance remain unclear. There is evidence that astrocytes are acutely sensitive to decreases in cerebral perfusion pressure and may function as intracranial baroreceptors, tuned to monitor brain blood flow. This study investigated the mechanosensory signaling in brainstem astrocytes, as these cells reside alongside the cardiovascular control circuits and mediate increases in blood pressure and heart rate induced by falls in brain perfusion. It was found that mechanical stimulation-evoked Ca 2+ responses in astrocytes of the rat brainstem were blocked by (1) antagonists of connexin channels, connexin 43 (Cx43) blocking peptide Gap26, or Cx43 gene knock-down; (2) antagonists of TRPV4 channels; (3) antagonist of P2Y 1 receptors for ATP; and (4) inhibitors of phospholipase C or IP3 receptors. Proximity ligation assay demonstrated interaction between TRPV4 and Cx43 channels in astrocytes. Dye loading experiments showed that mechanical stimulation increased open probability of carboxyfluorescein-permeable membrane channels. These data suggest that mechanosensory Ca 2+ responses in astrocytes are mediated by interaction between TRPV4 and Cx43 channels, leading to Cx43-mediated release of ATP which propagates/amplifies Ca 2+ signals via P2Y 1 receptors and Ca 2+ recruitment from the intracellular stores. In astrocyte-specific Cx43 knock-out mice the magnitude of heart rate responses to acute increases in intracranial pressure was not affected by Cx43 deficiency. However, these animals displayed lower heart rates at different levels of cerebral perfusion, supporting the hypothesis of connexin hemichannel-mediated release of signaling molecules by astrocytes having an excitatory action on the CNS sympathetic control circuits.

          SIGNIFICANCE STATEMENT There is evidence suggesting that astrocytes may function as intracranial baroreceptors that play an important role in the control of systemic and cerebral circulation. To function as intracranial baroreceptors, astrocytes must possess a specialized membrane mechanism that makes them exquisitely sensitive to mechanical stimuli. This study shows that opening of connexin 43 (Cx43) hemichannels leading to the release of ATP is the key central event underlying mechanosensory Ca 2+ responses in astrocytes. This astroglial mechanism plays an important role in the autonomic control of heart rate. These data add to the growing body of evidence suggesting that astrocytes function as versatile surveyors of the CNS metabolic milieu, tuned to detect conditions of potential metabolic threat, such as hypoxia, hypercapnia, and reduced perfusion.

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          Most cited references46

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          Glial regulation of the cerebral microvasculature.

          The brain is a heterogeneous organ with regionally varied and constantly changing energetic needs. Blood vessels in the brain are equipped with control mechanisms that match oxygen and glucose delivery through blood flow with the local metabolic demands that are imposed by neural activity. However, the cellular bases of this mechanism have remained elusive. A major advance has been the demonstration that astrocytes, cells with extensive contacts with both synapses and cerebral blood vessels, participate in the increases in flow evoked by synaptic activity. Their organization in nonoverlapping spatial domains indicates that they are uniquely positioned to shape the spatial distribution of the vascular responses that are evoked by neural activity. Astrocytic calcium is an important determinant of microvascular function and may regulate flow independently of synaptic activity. The involvement of astrocytes in neurovascular coupling has broad implications for the interpretation of functional imaging signals and for the understanding of brain diseases that are associated with neurovascular dysfunction.
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            Gliotransmitters travel in time and space.

            The identification of the presence of active signaling between astrocytes and neurons in a process termed gliotransmission has caused a paradigm shift in our thinking about brain function. However, we are still in the early days of the conceptualization of how astrocytes influence synapses, neurons, networks, and ultimately behavior. In this Perspective, our goal is to identify emerging principles governing gliotransmission and consider the specific properties of this process that endow the astrocyte with unique functions in brain signal integration. We develop and present hypotheses aimed at reconciling confounding reports and define open questions to provide a conceptual framework for future studies. We propose that astrocytes mainly signal through high-affinity slowly desensitizing receptors to modulate neurons and perform integration in spatiotemporal domains complementary to those of neurons. Copyright © 2014 Elsevier Inc. All rights reserved.
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              Characterizing proteins and their interactions in cells and tissues using the in situ proximity ligation assay.

              The activity of proteins is typically regulated by secondary modifications and by interactions with other partners, resulting in the formation of protein complexes whose functions depend on the participating proteins. Accordingly, it is of central importance to monitor the presence of interaction complexes as well as their localization, thus providing information about the types of cells where the proteins are located and in what sub-cellular compartment these interactions occur. Several methods for visualizing protein interactions in situ have been developed during the last decade. These methods in most cases involve genetic constructs, and they have been successfully used in assays of living cell maintained in tissue culture, but they cannot easily be implemented in studies of clinical specimens. For such samples, affinity reagents like antibodies can be used to target the interacting proteins. In this review we will describe the in situ proximity ligation assays (in situ PLA), a method that is suitable for visualizing protein interactions in both tissue sections and in vitro cell lines, and we discuss research tasks when this or other method may be selected.
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                Author and article information

                Journal
                J Neurosci
                J Neurosci
                jneuro
                jneurosci
                J. Neurosci
                The Journal of Neuroscience
                Society for Neuroscience
                0270-6474
                1529-2401
                2 December 2020
                2 December 2020
                : 40
                : 49
                : 9364-9371
                Affiliations
                [1] 1Centre for Cardiovascular and Metabolic Neuroscience, Department of Neuroscience, Physiology & Pharmacology, University College London, London WC1E 6BT, United Kingdom
                [2] 2Department of Neuroscience, Tufts Neuroscience Institute, Tufts University School of Medicine, Boston, Massachusetts 02111
                [3] 3UCL Centre for Advanced Biomedical Imaging, Division of Medicine, University College London, London WC1E 6DD, United Kingdom
                [4] 4Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, London WC1N 3BG, United Kingdom
                [5] 5Department of Biomedical Sciences, University of Lausanne, Lausanne 1005, Switzerland
                [6] 6Physiology, Pharmacology, and Neuroscience, University of Bristol, Bristol BS8 1TD, United Kingdom
                Author notes
                Correspondence should be addressed to Alexander V. Gourine at a.gourine@ 123456ucl.ac.uk

                Author contributions: A.V.G. designed research; E.A.T., A.B., Y.Y., N.E., A.K., S.M.T., A.H., P.S.H., N.M., and A.V.G. performed research; A.G.T., M.F.L., and P.G.H. contributed unpublished reagents/analytic tools; E.A.T., A.K., P.S.H., and A.V.G. analyzed data; A.V.G. wrote the paper.

                *E.A.T., A.B., and Y.Y. contributed equally to this study as joint first authors.

                E.A.Turovsky's present address: Institute of Cell Biophysics, Federal Research Center “Pushchino Scientific Center for Biological Research” of the Russian Academy of Sciences, 142290 Pushchino, Russia.

                Author information
                https://orcid.org/0000-0002-5514-2669
                Article
                JN-RM-1249-20
                10.1523/JNEUROSCI.1249-20.2020
                7724146
                33122390
                656bbaa4-f9ed-48bc-afc0-dc8aa49c56f1
                Copyright © 2020 Turovsky et al.

                This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.

                History
                : 20 May 2020
                : 20 August 2020
                : 16 September 2020
                Funding
                Funded by: http://doi.org/10.13039/100010269Wellcome Trust (Wellcome)
                Award ID: 200893
                Funded by: http://doi.org/10.13039/501100000274British Heart Foundation (BHF)
                Award ID: PG/18/8/33540
                Funded by: http://doi.org/10.13039/100000002HHS | National Institutes of Health (NIH)
                Award ID: 5RO1 NS037585-22
                Award ID: 5RO1 NS107315-03
                Categories
                Research Articles
                Cellular/Molecular

                astrocytes,baroreceptor,cardiovascular,glia,mechanosensory,sympathetic

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