Monoclonal antibody Cat-315 detects a glycoform of receptor protein tyrosine phosphatase beta/phosphacan early in CNS development that localizes to extrasynaptic sites prior to synapse formation
Perineuronal nets (PNs) are lattice-like condensations of the extracellular matrix (ECM) that envelop synapses and decorate the surface of subsets of neurons in the CNS. Previous work has suggested that, despite the fact that PNs themselves are not visualized until later in development, some PN comp...
Gespeichert in:
Veröffentlicht in: | Neuroscience 2006-11, Vol.142 (4), p.1055-1069 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1069 |
---|---|
container_issue | 4 |
container_start_page | 1055 |
container_title | Neuroscience |
container_volume | 142 |
creator | Dino, M.R. Harroch, S. Hockfield, S. Matthews, R.T. |
description | Perineuronal nets (PNs) are lattice-like condensations of the extracellular matrix (ECM) that envelop synapses and decorate the surface of subsets of neurons in the CNS. Previous work has suggested that, despite the fact that PNs themselves are not visualized until later in development, some PN component molecules are expressed in the rodent CNS even before synaptogenesis. In the adult mammalian brain, monoclonal antibody Cat-315 recognizes a glycoform of aggrecan, a major component of PNs. In primary cortical cultures, a Cat-315-reactive chondroitin sulfate proteoglycan (CSPG) is also expressed on neuronal surfaces and is secreted into culture media as early as 24 h after plating. In this study, we show that in primary cortical cultures, the Cat-315 CSPG detected in early neural development is expressed in extrasynaptic sites prior to synapse formation. This suggests that ECM components in the CNS, as in the neuromuscular junction (NMJ), may prepattern neuronal surfaces prior to innervation. We further show that while the Cat-315-reactive carbohydrate decorates aggrecan in the adult, it decorates a different CSPG in the developing CNS. Using receptor protein tyrosine phosphatase beta (RPTPβ/protein tyrosine phosphatase zeta) knock-out mice and immunoprecipitation techniques, we demonstrate here that in the developing rodent brain Cat-315 recognizes RPTPβ isoforms. Our further examination of the Cat-315 epitope suggests that it is an O-mannose linked epitope in the HNK-1 family. The presence of the Cat-315 reactive carbohydrate on different PN components—RPTPβ and aggrecan—at different stages of synapse development suggests a potential role for this neuron-specific carbohydrate motif in synaptogenesis. |
doi_str_mv | 10.1016/j.neuroscience.2006.07.054 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_69024925</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0306452206009845</els_id><sourcerecordid>19374340</sourcerecordid><originalsourceid>FETCH-LOGICAL-c439t-4a90958ac984d53ad25c22499ac17b034833b519f9e115f0e3ce91106e0c00e03</originalsourceid><addsrcrecordid>eNqNkU2P0zAQhi0EYkvhLyALCW7p2rGdxNxQly9pgQNwtqbOhHWV2sF2V4Sfxy_DpZGWG_hiaeaZdz5eQp5xtuGMN5f7jcdjDMk69BY3NWPNhrUbpuQ9suJdK6pWSXmfrJhgTSVVXV-QRyntWXlKiofkgje601rJFfn1Ifhgx-BhpOCz24V-plvIleCK9pjR5kSBfhtnG4YQDzQMNKLFKYdIpxgyOk_zXKZxHul0E9J0AxkS0h1muFwCFjxFiONMC739-Lko3-IYpgP6THMpoGOwMLqfmGgOFH_kCGn2MGVnaXK5hKfoSseS_BMv-qdpILvgH5MHA4wJnyz_mnx98_rL9l11_ent--2r68pKoXMlQTOtOrC6k70S0NfK1rXUGixvd0zIToid4nrQyLkaGAqLmnPWILOMIRNr8uKsW9b-fsSUzcEli-MIHsMxmUazIlerf4Jci1YKeVJ8eQZtuV-KOJiy5QHibDgzJ6vN3vxttTlZbVhrTjauydOly3F3wP6udPG2AM8XAFI57hDBW5fuuK5uFRNN4a7OHJbj3TqMZmnXu-J0Nn1w_zPPb74V014</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>19374340</pqid></control><display><type>article</type><title>Monoclonal antibody Cat-315 detects a glycoform of receptor protein tyrosine phosphatase beta/phosphacan early in CNS development that localizes to extrasynaptic sites prior to synapse formation</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals Complete</source><creator>Dino, M.R. ; Harroch, S. ; Hockfield, S. ; Matthews, R.T.</creator><creatorcontrib>Dino, M.R. ; Harroch, S. ; Hockfield, S. ; Matthews, R.T.</creatorcontrib><description>Perineuronal nets (PNs) are lattice-like condensations of the extracellular matrix (ECM) that envelop synapses and decorate the surface of subsets of neurons in the CNS. Previous work has suggested that, despite the fact that PNs themselves are not visualized until later in development, some PN component molecules are expressed in the rodent CNS even before synaptogenesis. In the adult mammalian brain, monoclonal antibody Cat-315 recognizes a glycoform of aggrecan, a major component of PNs. In primary cortical cultures, a Cat-315-reactive chondroitin sulfate proteoglycan (CSPG) is also expressed on neuronal surfaces and is secreted into culture media as early as 24 h after plating. In this study, we show that in primary cortical cultures, the Cat-315 CSPG detected in early neural development is expressed in extrasynaptic sites prior to synapse formation. This suggests that ECM components in the CNS, as in the neuromuscular junction (NMJ), may prepattern neuronal surfaces prior to innervation. We further show that while the Cat-315-reactive carbohydrate decorates aggrecan in the adult, it decorates a different CSPG in the developing CNS. Using receptor protein tyrosine phosphatase beta (RPTPβ/protein tyrosine phosphatase zeta) knock-out mice and immunoprecipitation techniques, we demonstrate here that in the developing rodent brain Cat-315 recognizes RPTPβ isoforms. Our further examination of the Cat-315 epitope suggests that it is an O-mannose linked epitope in the HNK-1 family. The presence of the Cat-315 reactive carbohydrate on different PN components—RPTPβ and aggrecan—at different stages of synapse development suggests a potential role for this neuron-specific carbohydrate motif in synaptogenesis.</description><identifier>ISSN: 0306-4522</identifier><identifier>EISSN: 1873-7544</identifier><identifier>DOI: 10.1016/j.neuroscience.2006.07.054</identifier><identifier>PMID: 16989954</identifier><identifier>CODEN: NRSCDN</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>aggrecan ; Aggrecans - chemistry ; Aggrecans - immunology ; Aggrecans - metabolism ; Amino Acid Motifs - immunology ; Animals ; Antibodies, Monoclonal - immunology ; Antibody Specificity - immunology ; Biological and medical sciences ; CD57 Antigens - chemistry ; CD57 Antigens - immunology ; Cell Differentiation - physiology ; Cells, Cultured ; Central Nervous System - embryology ; Central Nervous System - growth & development ; Central Nervous System - ultrastructure ; Chondroitin Sulfate Proteoglycans - chemistry ; Chondroitin Sulfate Proteoglycans - immunology ; Chondroitin Sulfate Proteoglycans - metabolism ; CSPGs ; Epitopes - chemistry ; Epitopes - immunology ; extracellular matrix ; Extracellular Matrix - metabolism ; Fundamental and applied biological sciences. Psychology ; Growth Cones - metabolism ; Growth Cones - ultrastructure ; Immunohistochemistry - methods ; Mice ; Mice, Knockout ; perineuronal net ; phosphacan ; Protein Tyrosine Phosphatases - chemistry ; Protein Tyrosine Phosphatases - genetics ; Protein Tyrosine Phosphatases - immunology ; Rats ; Rats, Sprague-Dawley ; Receptor-Like Protein Tyrosine Phosphatases, Class 5 ; RPTPβ ; Synapses - metabolism ; Synapses - ultrastructure ; Vertebrates: nervous system and sense organs</subject><ispartof>Neuroscience, 2006-11, Vol.142 (4), p.1055-1069</ispartof><rights>2006 IBRO</rights><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c439t-4a90958ac984d53ad25c22499ac17b034833b519f9e115f0e3ce91106e0c00e03</citedby><cites>FETCH-LOGICAL-c439t-4a90958ac984d53ad25c22499ac17b034833b519f9e115f0e3ce91106e0c00e03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.neuroscience.2006.07.054$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18275036$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16989954$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dino, M.R.</creatorcontrib><creatorcontrib>Harroch, S.</creatorcontrib><creatorcontrib>Hockfield, S.</creatorcontrib><creatorcontrib>Matthews, R.T.</creatorcontrib><title>Monoclonal antibody Cat-315 detects a glycoform of receptor protein tyrosine phosphatase beta/phosphacan early in CNS development that localizes to extrasynaptic sites prior to synapse formation</title><title>Neuroscience</title><addtitle>Neuroscience</addtitle><description>Perineuronal nets (PNs) are lattice-like condensations of the extracellular matrix (ECM) that envelop synapses and decorate the surface of subsets of neurons in the CNS. Previous work has suggested that, despite the fact that PNs themselves are not visualized until later in development, some PN component molecules are expressed in the rodent CNS even before synaptogenesis. In the adult mammalian brain, monoclonal antibody Cat-315 recognizes a glycoform of aggrecan, a major component of PNs. In primary cortical cultures, a Cat-315-reactive chondroitin sulfate proteoglycan (CSPG) is also expressed on neuronal surfaces and is secreted into culture media as early as 24 h after plating. In this study, we show that in primary cortical cultures, the Cat-315 CSPG detected in early neural development is expressed in extrasynaptic sites prior to synapse formation. This suggests that ECM components in the CNS, as in the neuromuscular junction (NMJ), may prepattern neuronal surfaces prior to innervation. We further show that while the Cat-315-reactive carbohydrate decorates aggrecan in the adult, it decorates a different CSPG in the developing CNS. Using receptor protein tyrosine phosphatase beta (RPTPβ/protein tyrosine phosphatase zeta) knock-out mice and immunoprecipitation techniques, we demonstrate here that in the developing rodent brain Cat-315 recognizes RPTPβ isoforms. Our further examination of the Cat-315 epitope suggests that it is an O-mannose linked epitope in the HNK-1 family. The presence of the Cat-315 reactive carbohydrate on different PN components—RPTPβ and aggrecan—at different stages of synapse development suggests a potential role for this neuron-specific carbohydrate motif in synaptogenesis.</description><subject>aggrecan</subject><subject>Aggrecans - chemistry</subject><subject>Aggrecans - immunology</subject><subject>Aggrecans - metabolism</subject><subject>Amino Acid Motifs - immunology</subject><subject>Animals</subject><subject>Antibodies, Monoclonal - immunology</subject><subject>Antibody Specificity - immunology</subject><subject>Biological and medical sciences</subject><subject>CD57 Antigens - chemistry</subject><subject>CD57 Antigens - immunology</subject><subject>Cell Differentiation - physiology</subject><subject>Cells, Cultured</subject><subject>Central Nervous System - embryology</subject><subject>Central Nervous System - growth & development</subject><subject>Central Nervous System - ultrastructure</subject><subject>Chondroitin Sulfate Proteoglycans - chemistry</subject><subject>Chondroitin Sulfate Proteoglycans - immunology</subject><subject>Chondroitin Sulfate Proteoglycans - metabolism</subject><subject>CSPGs</subject><subject>Epitopes - chemistry</subject><subject>Epitopes - immunology</subject><subject>extracellular matrix</subject><subject>Extracellular Matrix - metabolism</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Growth Cones - metabolism</subject><subject>Growth Cones - ultrastructure</subject><subject>Immunohistochemistry - methods</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>perineuronal net</subject><subject>phosphacan</subject><subject>Protein Tyrosine Phosphatases - chemistry</subject><subject>Protein Tyrosine Phosphatases - genetics</subject><subject>Protein Tyrosine Phosphatases - immunology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptor-Like Protein Tyrosine Phosphatases, Class 5</subject><subject>RPTPβ</subject><subject>Synapses - metabolism</subject><subject>Synapses - ultrastructure</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0306-4522</issn><issn>1873-7544</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU2P0zAQhi0EYkvhLyALCW7p2rGdxNxQly9pgQNwtqbOhHWV2sF2V4Sfxy_DpZGWG_hiaeaZdz5eQp5xtuGMN5f7jcdjDMk69BY3NWPNhrUbpuQ9suJdK6pWSXmfrJhgTSVVXV-QRyntWXlKiofkgje601rJFfn1Ifhgx-BhpOCz24V-plvIleCK9pjR5kSBfhtnG4YQDzQMNKLFKYdIpxgyOk_zXKZxHul0E9J0AxkS0h1muFwCFjxFiONMC739-Lko3-IYpgP6THMpoGOwMLqfmGgOFH_kCGn2MGVnaXK5hKfoSseS_BMv-qdpILvgH5MHA4wJnyz_mnx98_rL9l11_ent--2r68pKoXMlQTOtOrC6k70S0NfK1rXUGixvd0zIToid4nrQyLkaGAqLmnPWILOMIRNr8uKsW9b-fsSUzcEli-MIHsMxmUazIlerf4Jci1YKeVJ8eQZtuV-KOJiy5QHibDgzJ6vN3vxttTlZbVhrTjauydOly3F3wP6udPG2AM8XAFI57hDBW5fuuK5uFRNN4a7OHJbj3TqMZmnXu-J0Nn1w_zPPb74V014</recordid><startdate>20061103</startdate><enddate>20061103</enddate><creator>Dino, M.R.</creator><creator>Harroch, S.</creator><creator>Hockfield, S.</creator><creator>Matthews, R.T.</creator><general>Elsevier Ltd</general><general>Elsevier</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>7TK</scope><scope>7X8</scope></search><sort><creationdate>20061103</creationdate><title>Monoclonal antibody Cat-315 detects a glycoform of receptor protein tyrosine phosphatase beta/phosphacan early in CNS development that localizes to extrasynaptic sites prior to synapse formation</title><author>Dino, M.R. ; Harroch, S. ; Hockfield, S. ; Matthews, R.T.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c439t-4a90958ac984d53ad25c22499ac17b034833b519f9e115f0e3ce91106e0c00e03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>aggrecan</topic><topic>Aggrecans - chemistry</topic><topic>Aggrecans - immunology</topic><topic>Aggrecans - metabolism</topic><topic>Amino Acid Motifs - immunology</topic><topic>Animals</topic><topic>Antibodies, Monoclonal - immunology</topic><topic>Antibody Specificity - immunology</topic><topic>Biological and medical sciences</topic><topic>CD57 Antigens - chemistry</topic><topic>CD57 Antigens - immunology</topic><topic>Cell Differentiation - physiology</topic><topic>Cells, Cultured</topic><topic>Central Nervous System - embryology</topic><topic>Central Nervous System - growth & development</topic><topic>Central Nervous System - ultrastructure</topic><topic>Chondroitin Sulfate Proteoglycans - chemistry</topic><topic>Chondroitin Sulfate Proteoglycans - immunology</topic><topic>Chondroitin Sulfate Proteoglycans - metabolism</topic><topic>CSPGs</topic><topic>Epitopes - chemistry</topic><topic>Epitopes - immunology</topic><topic>extracellular matrix</topic><topic>Extracellular Matrix - metabolism</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Growth Cones - metabolism</topic><topic>Growth Cones - ultrastructure</topic><topic>Immunohistochemistry - methods</topic><topic>Mice</topic><topic>Mice, Knockout</topic><topic>perineuronal net</topic><topic>phosphacan</topic><topic>Protein Tyrosine Phosphatases - chemistry</topic><topic>Protein Tyrosine Phosphatases - genetics</topic><topic>Protein Tyrosine Phosphatases - immunology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptor-Like Protein Tyrosine Phosphatases, Class 5</topic><topic>RPTPβ</topic><topic>Synapses - metabolism</topic><topic>Synapses - ultrastructure</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dino, M.R.</creatorcontrib><creatorcontrib>Harroch, S.</creatorcontrib><creatorcontrib>Hockfield, S.</creatorcontrib><creatorcontrib>Matthews, R.T.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dino, M.R.</au><au>Harroch, S.</au><au>Hockfield, S.</au><au>Matthews, R.T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Monoclonal antibody Cat-315 detects a glycoform of receptor protein tyrosine phosphatase beta/phosphacan early in CNS development that localizes to extrasynaptic sites prior to synapse formation</atitle><jtitle>Neuroscience</jtitle><addtitle>Neuroscience</addtitle><date>2006-11-03</date><risdate>2006</risdate><volume>142</volume><issue>4</issue><spage>1055</spage><epage>1069</epage><pages>1055-1069</pages><issn>0306-4522</issn><eissn>1873-7544</eissn><coden>NRSCDN</coden><abstract>Perineuronal nets (PNs) are lattice-like condensations of the extracellular matrix (ECM) that envelop synapses and decorate the surface of subsets of neurons in the CNS. Previous work has suggested that, despite the fact that PNs themselves are not visualized until later in development, some PN component molecules are expressed in the rodent CNS even before synaptogenesis. In the adult mammalian brain, monoclonal antibody Cat-315 recognizes a glycoform of aggrecan, a major component of PNs. In primary cortical cultures, a Cat-315-reactive chondroitin sulfate proteoglycan (CSPG) is also expressed on neuronal surfaces and is secreted into culture media as early as 24 h after plating. In this study, we show that in primary cortical cultures, the Cat-315 CSPG detected in early neural development is expressed in extrasynaptic sites prior to synapse formation. This suggests that ECM components in the CNS, as in the neuromuscular junction (NMJ), may prepattern neuronal surfaces prior to innervation. We further show that while the Cat-315-reactive carbohydrate decorates aggrecan in the adult, it decorates a different CSPG in the developing CNS. Using receptor protein tyrosine phosphatase beta (RPTPβ/protein tyrosine phosphatase zeta) knock-out mice and immunoprecipitation techniques, we demonstrate here that in the developing rodent brain Cat-315 recognizes RPTPβ isoforms. Our further examination of the Cat-315 epitope suggests that it is an O-mannose linked epitope in the HNK-1 family. The presence of the Cat-315 reactive carbohydrate on different PN components—RPTPβ and aggrecan—at different stages of synapse development suggests a potential role for this neuron-specific carbohydrate motif in synaptogenesis.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>16989954</pmid><doi>10.1016/j.neuroscience.2006.07.054</doi><tpages>15</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0306-4522 |
ispartof | Neuroscience, 2006-11, Vol.142 (4), p.1055-1069 |
issn | 0306-4522 1873-7544 |
language | eng |
recordid | cdi_proquest_miscellaneous_69024925 |
source | MEDLINE; Elsevier ScienceDirect Journals Complete |
subjects | aggrecan Aggrecans - chemistry Aggrecans - immunology Aggrecans - metabolism Amino Acid Motifs - immunology Animals Antibodies, Monoclonal - immunology Antibody Specificity - immunology Biological and medical sciences CD57 Antigens - chemistry CD57 Antigens - immunology Cell Differentiation - physiology Cells, Cultured Central Nervous System - embryology Central Nervous System - growth & development Central Nervous System - ultrastructure Chondroitin Sulfate Proteoglycans - chemistry Chondroitin Sulfate Proteoglycans - immunology Chondroitin Sulfate Proteoglycans - metabolism CSPGs Epitopes - chemistry Epitopes - immunology extracellular matrix Extracellular Matrix - metabolism Fundamental and applied biological sciences. Psychology Growth Cones - metabolism Growth Cones - ultrastructure Immunohistochemistry - methods Mice Mice, Knockout perineuronal net phosphacan Protein Tyrosine Phosphatases - chemistry Protein Tyrosine Phosphatases - genetics Protein Tyrosine Phosphatases - immunology Rats Rats, Sprague-Dawley Receptor-Like Protein Tyrosine Phosphatases, Class 5 RPTPβ Synapses - metabolism Synapses - ultrastructure Vertebrates: nervous system and sense organs |
title | Monoclonal antibody Cat-315 detects a glycoform of receptor protein tyrosine phosphatase beta/phosphacan early in CNS development that localizes to extrasynaptic sites prior to synapse formation |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T05%3A50%3A22IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Monoclonal%20antibody%20Cat-315%20detects%20a%20glycoform%20of%20receptor%20protein%20tyrosine%20phosphatase%20beta/phosphacan%20early%20in%20CNS%20development%20that%20localizes%20to%20extrasynaptic%20sites%20prior%20to%20synapse%20formation&rft.jtitle=Neuroscience&rft.au=Dino,%20M.R.&rft.date=2006-11-03&rft.volume=142&rft.issue=4&rft.spage=1055&rft.epage=1069&rft.pages=1055-1069&rft.issn=0306-4522&rft.eissn=1873-7544&rft.coden=NRSCDN&rft_id=info:doi/10.1016/j.neuroscience.2006.07.054&rft_dat=%3Cproquest_cross%3E19374340%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=19374340&rft_id=info:pmid/16989954&rft_els_id=S0306452206009845&rfr_iscdi=true |