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      Astrocytes mediate synapse elimination through MEGF10 and MERTK pathways

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          Abstract

          To achieve its precise neural connectivity, the developing mammalian nervous system undergoes extensive activity-dependent synapse remodeling. Recently microglial cells have been shown to be responsible for a portion of synaptic remodeling, but the remaining mechanisms remain mysterious. Here we report a new role for astrocytes in actively engulfing CNS synapses. This process helps to mediate synapse elimination, requires the Megf10 and Mertk phagocytic pathways, and is strongly dependent on neuronal activity. Developing mice deficient in both astrocyte pathways fail to normally refine their retinogeniculate connections and retain excess functional synapses. Lastly, we show that in the adult mouse brain, astrocytes continuously engulf both excitatory and inhibitory synapses. These studies reveal a novel role for astrocytes in mediating synapse elimination in the developing and adult brain, identify Megf10 and Mertk as critical players in the synapse remodeling underlying neural circuit refinement, and have important implications for understanding learning and memory as well as neurological disease processes.

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          Most cited references22

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          Development of a method for the purification and culture of rodent astrocytes.

          The inability to purify and culture astrocytes has long hindered studies of their function. Whereas astrocyte progenitor cells can be cultured from neonatal brain, culture of mature astrocytes from postnatal brain has not been possible. Here, we report a new method to prospectively purify astrocytes by immunopanning. These astrocytes undergo apoptosis in culture, but vascular cells and HBEGF promote their survival in serum-free culture. We found that some developing astrocytes normally undergo apoptosis in vivo and that the vast majority of astrocytes contact blood vessels, suggesting that astrocytes are matched to blood vessels by competing for vascular-derived trophic factors such as HBEGF. Compared to traditional astrocyte cultures, the gene profiles of the cultured purified postnatal astrocytes much more closely resemble those of in vivo astrocytes. Although these astrocytes strongly promote synapse formation and function, they do not secrete glutamate in response to stimulation. Copyright © 2011 Elsevier Inc. All rights reserved.
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            Single-synapse analysis of a diverse synapse population: proteomic imaging methods and markers.

            A lack of methods for measuring the protein compositions of individual synapses in situ has so far hindered the exploration and exploitation of synapse molecular diversity. Here, we describe the use of array tomography, a new high-resolution proteomic imaging method, to determine the composition of glutamate and GABA synapses in somatosensory cortex of Line-H-YFP Thy-1 transgenic mice. We find that virtually all synapses are recognized by antibodies to the presynaptic phosphoprotein synapsin I, while antibodies to 16 other synaptic proteins discriminate among 4 subtypes of glutamatergic synapses and GABAergic synapses. Cell-specific YFP expression in the YFP-H mouse line allows synapses to be assigned to specific presynaptic and postsynaptic partners and reveals that a subpopulation of spines on layer 5 pyramidal cells receives both VGluT1-subtype glutamatergic and GABAergic synaptic inputs. These results establish a means for the high-throughput acquisition of proteomic data from individual cortical synapses in situ. Copyright © 2010 Elsevier Inc. All rights reserved.
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              A rapid Percoll gradient procedure for preparation of synaptosomes.

              Homogenization of fresh brain tissue in isotonic medium shears plasma membranes causing nerve terminals to become separated from their axons and postsynaptic connections. The nerve terminal membranes then reseal to form synaptosomes. The discontinuous Percoll gradient procedure described here is designed to isolate synaptosomes from brain homogenates in the minimum time to allow functional experiments to be performed. Synaptosomes are isolated using a medium-speed centrifuge, while maintaining isotonic conditions and minimizing mechanically damaging resuspension steps. This protocol has advantages over other procedures in terms of speed and by producing relatively homogeneous synaptosomes, minimizing the presence of synaptic and glial plasma membranes and extrasynaptosomal mitochondria. The purified synaptosomes are viable and take up and release neurotransmitters very efficiently. A typical yield of synaptosomes is between 2.5 and 4 mg of synaptosomal protein per gram rat brain. The procedure takes approximately 1 h from homogenization of the brain until collection of the synaptosomal suspension from the Percoll gradient.
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                Author and article information

                Journal
                0410462
                6011
                Nature
                Nature
                Nature
                0028-0836
                1476-4687
                11 March 2014
                24 November 2013
                19 December 2013
                19 June 2014
                : 504
                : 7480
                : 394-400
                Affiliations
                [1 ]Department of Neurobiology, Stanford University, School of Medicine, Stanford, CA 94305, USA
                [2 ]Department of Molecular and Cellular Physiology, Stanford University, School of Medicine, Stanford, CA 94305, USA
                [3 ]Department of Ophthalmology and Visual Sciences, University of Michigan, Ann Arbor, MI 48105, USA
                [4 ]Santa Cruz Institute of Particle Physic and Department of Physics, University of California, Santa Cruz, CA 95064
                [5 ]Institute of Molecular and Cell Biology, A*Star, 61 Biopolis Drive, Proteos Building, Singapore 138673
                [6 ]Children's Hospital, Harvard Medical School, 300 Longwood Ave., CLS12250, Boston, MA 02115
                Author notes
                Corresponding author: Chung, Won-Suk ( wschung@ 123456stanford.edu )
                Article
                NIHMS531479
                10.1038/nature12776
                3969024
                24270812
                80d2c2a9-aa19-46b7-aad2-ae404ccad0ea

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