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 |
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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 |
format | Article |
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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.</description><identifier>ISSN: 0028-0836</identifier><identifier>EISSN: 1476-4687</identifier><identifier>DOI: 10.1038/nature12776</identifier><identifier>PMID: 24270812</identifier><identifier>CODEN: NATUAS</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>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</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&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. 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.</description><subject>13/1</subject><subject>13/106</subject><subject>13/31</subject><subject>13/51</subject><subject>14/19</subject><subject>14/28</subject><subject>631/378/2596/1308</subject><subject>64/110</subject><subject>9/74</subject><subject>Animals</subject><subject>Astrocytes</subject><subject>Astrocytes - cytology</subject><subject>Astrocytes - metabolism</subject><subject>Biological and medical sciences</subject><subject>Brain - cytology</subject><subject>c-Mer Tyrosine Kinase</subject><subject>Cellular signal transduction</subject><subject>Central nervous system</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene expression</subject><subject>Health aspects</subject><subject>Humanities and Social Sciences</subject><subject>In Vitro Techniques</subject><subject>Insects</subject><subject>Kinases</subject><subject>Laboratory animals</subject><subject>Lateral Thalamic Nuclei - cytology</subject><subject>Lateral Thalamic Nuclei - metabolism</subject><subject>Learning - physiology</subject><subject>Membrane Proteins - deficiency</subject><subject>Membrane Proteins - genetics</subject><subject>Membrane Proteins - metabolism</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>Microscopy</subject><subject>multidisciplinary</subject><subject>Neural circuitry</subject><subject>Neural Pathways - cytology</subject><subject>Neural Pathways - metabolism</subject><subject>Phagocytosis</subject><subject>Physiological aspects</subject><subject>Protein expression</subject><subject>Proteins</subject><subject>Proto-Oncogene Proteins - deficiency</subject><subject>Proto-Oncogene Proteins - genetics</subject><subject>Proto-Oncogene Proteins - metabolism</subject><subject>Receptor Protein-Tyrosine Kinases - deficiency</subject><subject>Receptor Protein-Tyrosine Kinases - genetics</subject><subject>Receptor Protein-Tyrosine Kinases - metabolism</subject><subject>Retina - physiology</subject><subject>Science</subject><subject>Synapses</subject><subject>Synapses - metabolism</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0028-0836</issn><issn>1476-4687</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNpt0s9v0zAUB3ALgVgpnLijiAkJBBm24zjOBama9ksMIY1xtlznJfWU2J3tAP3vcdWytajKIZH9yfe9OA-h1wSfEFyIz1bF0QOhVcWfoAlhFc8ZF9VTNMGYihyLgh-hFyHcYYxLUrHn6IgyWmFB6ARdzkL0Tq8ihGyAxqgIWVhZtQyQQW8Gk9KNs1lceDd2i-zb2cU5wZmyTXq8uf2aLVVc_Far8BI9a1Uf4NX2PkU_z89uTy_z6-8XV6ez61xzRmPeEFWSco6VEtCIBrOmbucNp6UuoOa4nUOtBa_aomm5Tm3qgoCqS9XWuOCEQDFFXza5y3GeGtZgo1e9XHozKL-SThm5v2PNQnbulyxqXmPKUsD7bYB39yOEKAcTNPS9suDGIAmrcVUwkgpO0fF_9M6N3qbPSyodoEh59FF1qgdpbOtSXb0OlTNeUFZzKkhS-QHVgYXUpLPQmrS8598e8Hpp7uUuOjmA0tXAYPTB1A97LyQT4U_s1BiCvPpxs28_bqz2LgQP7cMhEyzXkyd3Ji_pN7v_5cH-G7UE3m2BClr1rVdWm_DoRBpOwdZlP21cSFu2A79z6Afq_gVxPe0H</recordid><startdate>20131219</startdate><enddate>20131219</enddate><creator>Chung, Won-Suk</creator><creator>Clarke, Laura E.</creator><creator>Wang, Gordon X.</creator><creator>Stafford, Benjamin K.</creator><creator>Sher, Alexander</creator><creator>Chakraborty, Chandrani</creator><creator>Joung, Julia</creator><creator>Foo, Lynette C.</creator><creator>Thompson, Andrew</creator><creator>Chen, Chinfei</creator><creator>Smith, Stephen J.</creator><creator>Barres, Ben A.</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7T5</scope><scope>7TG</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88G</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>BKSAR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M2O</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PCBAR</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PSYQQ</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>Q9U</scope><scope>R05</scope><scope>RC3</scope><scope>S0X</scope><scope>SOI</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20131219</creationdate><title>Astrocytes mediate synapse elimination through MEGF10 and MERTK pathways</title><author>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.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c642t-d1a515b0aa8ed8d04d9fbd625c3e960fbe9c867f3df6c242c31ea95af903611e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>13/1</topic><topic>13/106</topic><topic>13/31</topic><topic>13/51</topic><topic>14/19</topic><topic>14/28</topic><topic>631/378/2596/1308</topic><topic>64/110</topic><topic>9/74</topic><topic>Animals</topic><topic>Astrocytes</topic><topic>Astrocytes - 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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> |
fulltext | fulltext |
identifier | ISSN: 0028-0836 |
ispartof | Nature (London), 2013-12, Vol.504 (7480), p.394-400 |
issn | 0028-0836 1476-4687 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3969024 |
source | MEDLINE; Nature; Alma/SFX Local Collection |
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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