Astrocytes mediate synapse elimination through MEGF10 and MERTK pathways

To achieve its precise neural connectivity, the developing mammalian nervous system undergoes extensive activity-dependent synapse remodelling. Recently, microglial cells have been shown to be responsible for a portion of synaptic pruning, but the remaining mechanisms remain unknown. Here we report...

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Veröffentlicht in:Nature (London) 2013-12, Vol.504 (7480), p.394-400
Hauptverfasser: Chung, Won-Suk, Clarke, Laura E., Wang, Gordon X., Stafford, Benjamin K., Sher, Alexander, Chakraborty, Chandrani, Joung, Julia, Foo, Lynette C., Thompson, Andrew, Chen, Chinfei, Smith, Stephen J., Barres, Ben A.
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container_issue 7480
container_start_page 394
container_title Nature (London)
container_volume 504
creator Chung, Won-Suk
Clarke, Laura E.
Wang, Gordon X.
Stafford, Benjamin K.
Sher, Alexander
Chakraborty, Chandrani
Joung, Julia
Foo, Lynette C.
Thompson, Andrew
Chen, Chinfei
Smith, Stephen J.
Barres, Ben A.
description To achieve its precise neural connectivity, the developing mammalian nervous system undergoes extensive activity-dependent synapse remodelling. Recently, microglial cells have been shown to be responsible for a portion of synaptic pruning, but the remaining mechanisms remain unknown. Here we report a new role for astrocytes in actively engulfing central nervous system 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 refine their retinogeniculate connections normally and retain excess functional synapses. Finally, 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 proteins in the synapse remodelling underlying neural circuit refinement, and have important implications for understanding learning and memory as well as neurological disease processes. This study describes comprehensive synaptic engulfment by astrocytes, mediating synapse elimination in an activity-dependent manner; this elimination process involves the MEGF10 and MERTK phagocytic pathways and persists into adulthood, with mutant mice that lack these pathways in astrocytes exhibiting a failure to refine retinogeniculate connections during development. Astrocytes involved in synapse elimination Synapse elimination is an important aspect of brain development in which the number of synaptic contacts is reduced in an activity-dependent manner. Glial cells — non-neural cells that perform a variety of roles in the brain — were recently shown to have a role in synapse remodelling, with the phagocytic microglia responsible for a certain proportion of connection refinement, with little else known regarding the mechanisms underlying this. Here, Won-Suk Chung et al . describe comprehensive synaptic engulfment by astrocytes, mediating synapse elimination in an activity-dependent manner. This elimination process involved the MEGF10 and MERTK phagocytic pathways, with transgenic animals lacking these pathways in astrocytes exhibiting a failure to refine retinogeniculate connections during development. These mechanisms also extend into adulthood. This work has implications for our understanding of learning and memory as well as ne
doi_str_mv 10.1038/nature12776
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Recently, microglial cells have been shown to be responsible for a portion of synaptic pruning, but the remaining mechanisms remain unknown. Here we report a new role for astrocytes in actively engulfing central nervous system 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 refine their retinogeniculate connections normally and retain excess functional synapses. Finally, 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 proteins in the synapse remodelling underlying neural circuit refinement, and have important implications for understanding learning and memory as well as neurological disease processes. This study describes comprehensive synaptic engulfment by astrocytes, mediating synapse elimination in an activity-dependent manner; this elimination process involves the MEGF10 and MERTK phagocytic pathways and persists into adulthood, with mutant mice that lack these pathways in astrocytes exhibiting a failure to refine retinogeniculate connections during development. Astrocytes involved in synapse elimination Synapse elimination is an important aspect of brain development in which the number of synaptic contacts is reduced in an activity-dependent manner. Glial cells — non-neural cells that perform a variety of roles in the brain — were recently shown to have a role in synapse remodelling, with the phagocytic microglia responsible for a certain proportion of connection refinement, with little else known regarding the mechanisms underlying this. Here, Won-Suk Chung et al . describe comprehensive synaptic engulfment by astrocytes, mediating synapse elimination in an activity-dependent manner. This elimination process involved the MEGF10 and MERTK phagocytic pathways, with transgenic animals lacking these pathways in astrocytes exhibiting a failure to refine retinogeniculate connections during development. These mechanisms also extend into adulthood. 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Psychology ; Gene expression ; Health aspects ; Humanities and Social Sciences ; In Vitro Techniques ; Insects ; Kinases ; Laboratory animals ; Lateral Thalamic Nuclei - cytology ; Lateral Thalamic Nuclei - metabolism ; Learning - physiology ; Membrane Proteins - deficiency ; Membrane Proteins - genetics ; Membrane Proteins - metabolism ; Mice ; Mice, Transgenic ; Microscopy ; multidisciplinary ; Neural circuitry ; Neural Pathways - cytology ; Neural Pathways - metabolism ; Phagocytosis ; Physiological aspects ; Protein expression ; Proteins ; Proto-Oncogene Proteins - deficiency ; Proto-Oncogene Proteins - genetics ; Proto-Oncogene Proteins - metabolism ; Receptor Protein-Tyrosine Kinases - deficiency ; Receptor Protein-Tyrosine Kinases - genetics ; Receptor Protein-Tyrosine Kinases - metabolism ; Retina - physiology ; Science ; Synapses ; Synapses - metabolism ; Vertebrates: nervous system and sense organs</subject><ispartof>Nature (London), 2013-12, Vol.504 (7480), p.394-400</ispartof><rights>Springer Nature Limited 2013</rights><rights>2015 INIST-CNRS</rights><rights>COPYRIGHT 2013 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Dec 19-Dec 26, 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c642t-d1a515b0aa8ed8d04d9fbd625c3e960fbe9c867f3df6c242c31ea95af903611e3</citedby><cites>FETCH-LOGICAL-c642t-d1a515b0aa8ed8d04d9fbd625c3e960fbe9c867f3df6c242c31ea95af903611e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=28051841$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24270812$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chung, Won-Suk</creatorcontrib><creatorcontrib>Clarke, Laura E.</creatorcontrib><creatorcontrib>Wang, Gordon X.</creatorcontrib><creatorcontrib>Stafford, Benjamin K.</creatorcontrib><creatorcontrib>Sher, Alexander</creatorcontrib><creatorcontrib>Chakraborty, Chandrani</creatorcontrib><creatorcontrib>Joung, Julia</creatorcontrib><creatorcontrib>Foo, Lynette C.</creatorcontrib><creatorcontrib>Thompson, Andrew</creatorcontrib><creatorcontrib>Chen, Chinfei</creatorcontrib><creatorcontrib>Smith, Stephen J.</creatorcontrib><creatorcontrib>Barres, Ben A.</creatorcontrib><title>Astrocytes mediate synapse elimination through MEGF10 and MERTK pathways</title><title>Nature (London)</title><addtitle>Nature</addtitle><addtitle>Nature</addtitle><description>To achieve its precise neural connectivity, the developing mammalian nervous system undergoes extensive activity-dependent synapse remodelling. 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Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Earth, Atmospheric &amp; Aquatic Science Database</collection><collection>Materials Science Collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest One Psychology</collection><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>ProQuest Central Basic</collection><collection>University of Michigan</collection><collection>Genetics Abstracts</collection><collection>SIRS Editorial</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Nature (London)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chung, Won-Suk</au><au>Clarke, Laura E.</au><au>Wang, Gordon X.</au><au>Stafford, Benjamin K.</au><au>Sher, Alexander</au><au>Chakraborty, Chandrani</au><au>Joung, Julia</au><au>Foo, Lynette C.</au><au>Thompson, Andrew</au><au>Chen, Chinfei</au><au>Smith, Stephen J.</au><au>Barres, Ben A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Astrocytes mediate synapse elimination through MEGF10 and MERTK pathways</atitle><jtitle>Nature (London)</jtitle><stitle>Nature</stitle><addtitle>Nature</addtitle><date>2013-12-19</date><risdate>2013</risdate><volume>504</volume><issue>7480</issue><spage>394</spage><epage>400</epage><pages>394-400</pages><issn>0028-0836</issn><eissn>1476-4687</eissn><coden>NATUAS</coden><abstract>To achieve its precise neural connectivity, the developing mammalian nervous system undergoes extensive activity-dependent synapse remodelling. Recently, microglial cells have been shown to be responsible for a portion of synaptic pruning, but the remaining mechanisms remain unknown. Here we report a new role for astrocytes in actively engulfing central nervous system 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 refine their retinogeniculate connections normally and retain excess functional synapses. Finally, 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 proteins in the synapse remodelling underlying neural circuit refinement, and have important implications for understanding learning and memory as well as neurological disease processes. This study describes comprehensive synaptic engulfment by astrocytes, mediating synapse elimination in an activity-dependent manner; this elimination process involves the MEGF10 and MERTK phagocytic pathways and persists into adulthood, with mutant mice that lack these pathways in astrocytes exhibiting a failure to refine retinogeniculate connections during development. Astrocytes involved in synapse elimination Synapse elimination is an important aspect of brain development in which the number of synaptic contacts is reduced in an activity-dependent manner. Glial cells — non-neural cells that perform a variety of roles in the brain — were recently shown to have a role in synapse remodelling, with the phagocytic microglia responsible for a certain proportion of connection refinement, with little else known regarding the mechanisms underlying this. Here, Won-Suk Chung et al . describe comprehensive synaptic engulfment by astrocytes, mediating synapse elimination in an activity-dependent manner. This elimination process involved the MEGF10 and MERTK phagocytic pathways, with transgenic animals lacking these pathways in astrocytes exhibiting a failure to refine retinogeniculate connections during development. These mechanisms also extend into adulthood. This work has implications for our understanding of learning and memory as well as neurological disease processes.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>24270812</pmid><doi>10.1038/nature12776</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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subjects 13/1
13/106
13/31
13/51
14/19
14/28
631/378/2596/1308
64/110
9/74
Animals
Astrocytes
Astrocytes - cytology
Astrocytes - metabolism
Biological and medical sciences
Brain - cytology
c-Mer Tyrosine Kinase
Cellular signal transduction
Central nervous system
Fundamental and applied biological sciences. Psychology
Gene expression
Health aspects
Humanities and Social Sciences
In Vitro Techniques
Insects
Kinases
Laboratory animals
Lateral Thalamic Nuclei - cytology
Lateral Thalamic Nuclei - metabolism
Learning - physiology
Membrane Proteins - deficiency
Membrane Proteins - genetics
Membrane Proteins - metabolism
Mice
Mice, Transgenic
Microscopy
multidisciplinary
Neural circuitry
Neural Pathways - cytology
Neural Pathways - metabolism
Phagocytosis
Physiological aspects
Protein expression
Proteins
Proto-Oncogene Proteins - deficiency
Proto-Oncogene Proteins - genetics
Proto-Oncogene Proteins - metabolism
Receptor Protein-Tyrosine Kinases - deficiency
Receptor Protein-Tyrosine Kinases - genetics
Receptor Protein-Tyrosine Kinases - metabolism
Retina - physiology
Science
Synapses
Synapses - metabolism
Vertebrates: nervous system and sense organs
title Astrocytes mediate synapse elimination through MEGF10 and MERTK pathways
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