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      Microglia Regulate Pruning of Specialized Synapses in the Auditory Brainstem

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          Abstract

          The assembly of uniquely organized sound localization circuits in the brainstem requires precise developmental mechanisms. Glial cells have been shown to shape synaptic connections in the retinogeniculate system during development, but their contributions to specialized auditory synapses have not been identified. Here we investigated the role of microglia in auditory brainstem circuit assembly, focusing on the formation and pruning of the calyx of Held in the medial nucleus of the trapezoid body (MNTB). Microglia were pharmacologically depleted in mice early in development using subcutaneous injections of an inhibitor of colony stimulating factor 1 receptor, which is essential for microglia survival. Brainstems were examined prior to and just after hearing onset, at postnatal days (P) 8 and P13, respectively. We found that at P13 there were significantly more polyinnervated MNTB neurons when microglia were depleted, consistent with a defect in pruning. Expression of glial fibrillary acidic protein (GFAP), a mature astrocyte marker that normally appears in the MNTB late in development, was significantly decreased in microglia-depleted mice at P13, suggesting a delay in astrocyte maturation. Our results demonstrate that monoinnervation of MNTB neurons by the calyx of Held is significantly disrupted or delayed in the absence of microglia. This finding may reflect a direct role for microglia in synaptic pruning. A secondary role for microglia may be in the maturation of astrocytes in MNTB. These findings highlight the significant function of glia in pruning during calyx of Held development.

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          Cell Biology of Astrocyte-Synapse Interactions

          Astrocytes, the most abundant glial cells in the mammalian brain, are critical regulators of brain development and physiology through dynamic and often bidirectional interactions with neuronal synapses. Despite the clear importance of astrocytes for the establishment and maintenance of proper synaptic connectivity, our understanding of their role in brain function is still in its infancy. We propose that this is at least in part due to large gaps in our knowledge of the cell biology of astrocytes and the mechanisms they use to interact with synapses. In this review, we summarize some of the seminal findings that yield important insight into the cellular and molecular basis of astrocyte-neuron communication, focusing on the role of astrocytes in the development and remodeling of synapses. Furthermore, we will pose some pressing questions that need to be addressed to advance our mechanistic understanding of the role of astrocytes in regulating synaptic development.
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            Astrocytes Control Synapse Formation, Function, and Elimination.

            Astrocytes, through their close associations with synapses, can monitor and alter synaptic function, thus actively controlling synaptic transmission in the adult brain. Besides their important role at adult synapses, in the last three decades a number of critical findings have highlighted the importance of astrocytes in the establishment of synaptic connectivity in the developing brain. In this article, we will review the key findings on astrocytic control of synapse formation, function, and elimination. First, we will summarize our current structural and functional understanding of astrocytes at the synapse. Then, we will discuss the cellular and molecular mechanisms through which developing and mature astrocytes instruct the formation, maturation, and refinement of synapses. Our aim is to provide an overview of astrocytes as important players in the establishment of a functional nervous system.
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              The expression of vesicular glutamate transporters defines two classes of excitatory synapse.

              The quantal release of glutamate depends on its transport into synaptic vesicles. Recent work has shown that a protein previously implicated in the uptake of inorganic phosphate across the plasma membrane catalyzes glutamate uptake by synaptic vesicles. However, only a subset of glutamate neurons expresses this vesicular glutamate transporter (VGLUT1). We now report that excitatory neurons lacking VGLUT1 express a closely related protein that has also been implicated in phosphate transport. Like VGLUT1, this protein localizes to synaptic vesicles and functions as a vesicular glutamate transporter (VGLUT2). The complementary expression of VGLUT1 and 2 defines two distinct classes of excitatory synapse.
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                Author and article information

                Contributors
                Journal
                Front Neural Circuits
                Front Neural Circuits
                Front. Neural Circuits
                Frontiers in Neural Circuits
                Frontiers Media S.A.
                1662-5110
                28 August 2019
                2019
                : 13
                : 55
                Affiliations
                [1] 1Department of Neurobiology and Behavior, University of California, Irvine , Irvine, CA, United States
                [2] 2Vollum Institute, Oregon Health & Science University , Portland, OR, United States
                [3] 3Hearing Research, Garvan Institute of Medical Research , Sydney, NSW, Australia
                [4] 4St Vincent’s Clinical School, UNSW Sydney , Sydney, NSW, Australia
                Author notes

                Edited by: Catherine Carr, University of Maryland, College Park, United States

                Reviewed by: José M. Juiz, Universidad de Castilla–La Mancha, Spain; Diasynou Fioravante, University of California, Davis, United States

                *Correspondence: Karina S. Cramer, cramerk@ 123456uci.edu
                Article
                10.3389/fncir.2019.00055
                6722190
                31555101
                c8541968-24ce-40e8-bb36-7d775de52288
                Copyright © 2019 Milinkeviciute, Henningfield, Muniak, Chokr, Green and Cramer.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 17 May 2019
                : 30 July 2019
                Page count
                Figures: 10, Tables: 3, Equations: 0, References: 98, Pages: 19, Words: 0
                Funding
                Funded by: National Institute on Deafness and Other Communication Disorders 10.13039/100000055
                Award ID: R01 DC010796
                Funded by: National Institute of Neurological Disorders and Stroke 10.13039/100000065
                Award ID: R01 NS083801
                Funded by: National Institute on Aging 10.13039/100000049
                Award ID: R01 AG056768
                Funded by: National Cancer Center 10.13039/100008746
                Award ID: P30 CA062203
                Funded by: National Institute of General Medical Sciences 10.13039/100000057
                Award ID: P50 GM076516
                Categories
                Neuroscience
                Original Research

                Neurosciences
                microglia,calyx of held,mntb,pruning,auditory brainstem,csf1r inhibitors,depletion
                Neurosciences
                microglia, calyx of held, mntb, pruning, auditory brainstem, csf1r inhibitors, depletion

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