Gamma-protocadherins are targeted to subsets of synapses and intracellular organelles in neurons
The clustered protocadherins (Pcdhs) comprise >50 putative synaptic recognition molecules that are related to classical cadherins and highly expressed in the nervous system. Pcdhs are organized into three gene clusters (alpha, beta, and gamma). Within the alpha and gamma clusters, three exons enc...
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Veröffentlicht in: | The Journal of neuroscience 2003-06, Vol.23 (12), p.5096-5104 |
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description | The clustered protocadherins (Pcdhs) comprise >50 putative synaptic recognition molecules that are related to classical cadherins and highly expressed in the nervous system. Pcdhs are organized into three gene clusters (alpha, beta, and gamma). Within the alpha and gamma clusters, three exons encode the cytoplasmic domain for each Pcdh, making these domains identical within a cluster. Using an antibody to the Pcdh-gamma constant cytoplasmic domain, we find that all interneurons in cultured hippocampal neurons express high levels of Pcdh-gamma(s) in a nonsynaptic distribution. In contrast, only 48% of pyramidal-like cells expressed appreciable levels of these molecules. In these cells, Pcdh-gamma(s) were associated with a subset of excitatory synapses in which they may mediate presynaptic to postsynaptic recognition in concert with classical cadherins. Immunogold localization in hippocampal tissue showed Pcdh-gamma(s) at some synapses, in nonsynaptic plasma membranes, and in axonal and dendritic tubulovesicular structures, indicating that they may be exchanged among synapses and intracellular compartments. Our results show that although Pcdh-gamma(s) can be synaptic molecules, synapses form lacking Pcdh-gamma(s). Thus, Pcdh-gamma(s) and their relatives may be late additions to the classical cadherin-based synaptic adhesive scaffold; their presence in intracellular compartments suggests a role in modifying synaptic physiology or stability. |
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Pcdhs are organized into three gene clusters (alpha, beta, and gamma). Within the alpha and gamma clusters, three exons encode the cytoplasmic domain for each Pcdh, making these domains identical within a cluster. Using an antibody to the Pcdh-gamma constant cytoplasmic domain, we find that all interneurons in cultured hippocampal neurons express high levels of Pcdh-gamma(s) in a nonsynaptic distribution. In contrast, only 48% of pyramidal-like cells expressed appreciable levels of these molecules. In these cells, Pcdh-gamma(s) were associated with a subset of excitatory synapses in which they may mediate presynaptic to postsynaptic recognition in concert with classical cadherins. Immunogold localization in hippocampal tissue showed Pcdh-gamma(s) at some synapses, in nonsynaptic plasma membranes, and in axonal and dendritic tubulovesicular structures, indicating that they may be exchanged among synapses and intracellular compartments. Our results show that although Pcdh-gamma(s) can be synaptic molecules, synapses form lacking Pcdh-gamma(s). Thus, Pcdh-gamma(s) and their relatives may be late additions to the classical cadherin-based synaptic adhesive scaffold; their presence in intracellular compartments suggests a role in modifying synaptic physiology or stability.</description><identifier>ISSN: 0270-6474</identifier><identifier>EISSN: 1529-2401</identifier><identifier>DOI: 10.1523/jneurosci.23-12-05096.2003</identifier><identifier>PMID: 12832533</identifier><language>eng</language><publisher>United States: Society for Neuroscience</publisher><subject>Alternative Splicing ; Animals ; Antibody Specificity ; Cadherins - biosynthesis ; Cadherins - genetics ; Cadherins - metabolism ; Cell Adhesion - physiology ; Cells, Cultured ; Cellular/Molecular ; g-Protocadherin ; Glutamate Decarboxylase ; Hippocampus - cytology ; Immunohistochemistry ; Interneurons - cytology ; Interneurons - metabolism ; Mice ; Nerve Tissue Proteins - biosynthesis ; Neurons - cytology ; Neurons - metabolism ; Organelles - metabolism ; Protein Transport - physiology ; Pyramidal Cells - cytology ; Pyramidal Cells - metabolism ; Rats ; Signal Transduction - physiology ; Subcellular Fractions - metabolism ; Synapses - metabolism</subject><ispartof>The Journal of neuroscience, 2003-06, Vol.23 (12), p.5096-5104</ispartof><rights>Copyright © 2003 Society for Neuroscience 0270-6474/03/235096-09.00/0 2003</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c510t-957c46286d9e6428ff270f8c2c8f6ed611674b6eeb694c2d0b9e66c3e431afe83</citedby><cites>FETCH-LOGICAL-c510t-957c46286d9e6428ff270f8c2c8f6ed611674b6eeb694c2d0b9e66c3e431afe83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6741188/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6741188/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12832533$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Phillips, Greg R</creatorcontrib><creatorcontrib>Tanaka, Hidekazu</creatorcontrib><creatorcontrib>Frank, Marcus</creatorcontrib><creatorcontrib>Elste, Alice</creatorcontrib><creatorcontrib>Fidler, Lazar</creatorcontrib><creatorcontrib>Benson, Deanna L</creatorcontrib><creatorcontrib>Colman, David R</creatorcontrib><title>Gamma-protocadherins are targeted to subsets of synapses and intracellular organelles in neurons</title><title>The Journal of neuroscience</title><addtitle>J Neurosci</addtitle><description>The clustered protocadherins (Pcdhs) comprise >50 putative synaptic recognition molecules that are related to classical cadherins and highly expressed in the nervous system. Pcdhs are organized into three gene clusters (alpha, beta, and gamma). Within the alpha and gamma clusters, three exons encode the cytoplasmic domain for each Pcdh, making these domains identical within a cluster. Using an antibody to the Pcdh-gamma constant cytoplasmic domain, we find that all interneurons in cultured hippocampal neurons express high levels of Pcdh-gamma(s) in a nonsynaptic distribution. In contrast, only 48% of pyramidal-like cells expressed appreciable levels of these molecules. In these cells, Pcdh-gamma(s) were associated with a subset of excitatory synapses in which they may mediate presynaptic to postsynaptic recognition in concert with classical cadherins. Immunogold localization in hippocampal tissue showed Pcdh-gamma(s) at some synapses, in nonsynaptic plasma membranes, and in axonal and dendritic tubulovesicular structures, indicating that they may be exchanged among synapses and intracellular compartments. Our results show that although Pcdh-gamma(s) can be synaptic molecules, synapses form lacking Pcdh-gamma(s). Thus, Pcdh-gamma(s) and their relatives may be late additions to the classical cadherin-based synaptic adhesive scaffold; their presence in intracellular compartments suggests a role in modifying synaptic physiology or stability.</description><subject>Alternative Splicing</subject><subject>Animals</subject><subject>Antibody Specificity</subject><subject>Cadherins - biosynthesis</subject><subject>Cadherins - genetics</subject><subject>Cadherins - metabolism</subject><subject>Cell Adhesion - physiology</subject><subject>Cells, Cultured</subject><subject>Cellular/Molecular</subject><subject>g-Protocadherin</subject><subject>Glutamate Decarboxylase</subject><subject>Hippocampus - cytology</subject><subject>Immunohistochemistry</subject><subject>Interneurons - cytology</subject><subject>Interneurons - metabolism</subject><subject>Mice</subject><subject>Nerve Tissue Proteins - biosynthesis</subject><subject>Neurons - cytology</subject><subject>Neurons - metabolism</subject><subject>Organelles - metabolism</subject><subject>Protein Transport - physiology</subject><subject>Pyramidal Cells - cytology</subject><subject>Pyramidal Cells - metabolism</subject><subject>Rats</subject><subject>Signal Transduction - physiology</subject><subject>Subcellular Fractions - metabolism</subject><subject>Synapses - metabolism</subject><issn>0270-6474</issn><issn>1529-2401</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1r3DAQxUVoSTYf_0IRPfTmjUaSZbuHQlk2X4QG2uSsyPJ442BLW8kO5L-PnCxteuppGOY3j_d4hHwGtoSci9NHh1Pw0XZLLjLgGctZpZacMbFHFomoMi4ZfCALxguWKVnIA3IY4yNjrGBQ7JMD4KXguRALcn9uhsFk2-BHb03zgKFzkZqAdDRhgyM2dPQ0TnXEMVLf0vjszDZiYlxDOzcGY7Hvp94E6sPGuLSkY-foq0kXj8nH1vQRT3bziNydrW9XF9n1zfnl6vt1ZnNgY1blhZWKl6qpUEletm3y3paW27JV2CgAVchaIdaqkpY3rE6csgKlANNiKY7Itzfd7VQP2FicrfV6G7rBhGftTaf_vbjuQW_8k066AOUs8GUnEPzvCeOohy7O2VImP0VdCMk5VPy_IJSVqIocEvj1DbSprRiw_eMGmJ6b1Fc_1nc_b36tLnVagOvXJvXcZHr-9D7P39dddeIFhTufgw</recordid><startdate>20030615</startdate><enddate>20030615</enddate><creator>Phillips, Greg R</creator><creator>Tanaka, Hidekazu</creator><creator>Frank, Marcus</creator><creator>Elste, Alice</creator><creator>Fidler, Lazar</creator><creator>Benson, Deanna L</creator><creator>Colman, David R</creator><general>Society for Neuroscience</general><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><scope>5PM</scope></search><sort><creationdate>20030615</creationdate><title>Gamma-protocadherins are targeted to subsets of synapses and intracellular organelles in neurons</title><author>Phillips, Greg R ; Tanaka, Hidekazu ; Frank, Marcus ; Elste, Alice ; Fidler, Lazar ; Benson, Deanna L ; Colman, David R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c510t-957c46286d9e6428ff270f8c2c8f6ed611674b6eeb694c2d0b9e66c3e431afe83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Alternative Splicing</topic><topic>Animals</topic><topic>Antibody Specificity</topic><topic>Cadherins - biosynthesis</topic><topic>Cadherins - genetics</topic><topic>Cadherins - metabolism</topic><topic>Cell Adhesion - physiology</topic><topic>Cells, Cultured</topic><topic>Cellular/Molecular</topic><topic>g-Protocadherin</topic><topic>Glutamate Decarboxylase</topic><topic>Hippocampus - cytology</topic><topic>Immunohistochemistry</topic><topic>Interneurons - cytology</topic><topic>Interneurons - metabolism</topic><topic>Mice</topic><topic>Nerve Tissue Proteins - biosynthesis</topic><topic>Neurons - cytology</topic><topic>Neurons - metabolism</topic><topic>Organelles - metabolism</topic><topic>Protein Transport - physiology</topic><topic>Pyramidal Cells - cytology</topic><topic>Pyramidal Cells - metabolism</topic><topic>Rats</topic><topic>Signal Transduction - physiology</topic><topic>Subcellular Fractions - metabolism</topic><topic>Synapses - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Phillips, Greg R</creatorcontrib><creatorcontrib>Tanaka, Hidekazu</creatorcontrib><creatorcontrib>Frank, Marcus</creatorcontrib><creatorcontrib>Elste, Alice</creatorcontrib><creatorcontrib>Fidler, Lazar</creatorcontrib><creatorcontrib>Benson, Deanna L</creatorcontrib><creatorcontrib>Colman, David R</creatorcontrib><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><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Phillips, Greg R</au><au>Tanaka, Hidekazu</au><au>Frank, Marcus</au><au>Elste, Alice</au><au>Fidler, Lazar</au><au>Benson, Deanna L</au><au>Colman, David R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Gamma-protocadherins are targeted to subsets of synapses and intracellular organelles in neurons</atitle><jtitle>The Journal of neuroscience</jtitle><addtitle>J Neurosci</addtitle><date>2003-06-15</date><risdate>2003</risdate><volume>23</volume><issue>12</issue><spage>5096</spage><epage>5104</epage><pages>5096-5104</pages><issn>0270-6474</issn><eissn>1529-2401</eissn><abstract>The clustered protocadherins (Pcdhs) comprise >50 putative synaptic recognition molecules that are related to classical cadherins and highly expressed in the nervous system. Pcdhs are organized into three gene clusters (alpha, beta, and gamma). Within the alpha and gamma clusters, three exons encode the cytoplasmic domain for each Pcdh, making these domains identical within a cluster. Using an antibody to the Pcdh-gamma constant cytoplasmic domain, we find that all interneurons in cultured hippocampal neurons express high levels of Pcdh-gamma(s) in a nonsynaptic distribution. In contrast, only 48% of pyramidal-like cells expressed appreciable levels of these molecules. In these cells, Pcdh-gamma(s) were associated with a subset of excitatory synapses in which they may mediate presynaptic to postsynaptic recognition in concert with classical cadherins. Immunogold localization in hippocampal tissue showed Pcdh-gamma(s) at some synapses, in nonsynaptic plasma membranes, and in axonal and dendritic tubulovesicular structures, indicating that they may be exchanged among synapses and intracellular compartments. Our results show that although Pcdh-gamma(s) can be synaptic molecules, synapses form lacking Pcdh-gamma(s). Thus, Pcdh-gamma(s) and their relatives may be late additions to the classical cadherin-based synaptic adhesive scaffold; their presence in intracellular compartments suggests a role in modifying synaptic physiology or stability.</abstract><cop>United States</cop><pub>Society for Neuroscience</pub><pmid>12832533</pmid><doi>10.1523/jneurosci.23-12-05096.2003</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Alternative Splicing Animals Antibody Specificity Cadherins - biosynthesis Cadherins - genetics Cadherins - metabolism Cell Adhesion - physiology Cells, Cultured Cellular/Molecular g-Protocadherin Glutamate Decarboxylase Hippocampus - cytology Immunohistochemistry Interneurons - cytology Interneurons - metabolism Mice Nerve Tissue Proteins - biosynthesis Neurons - cytology Neurons - metabolism Organelles - metabolism Protein Transport - physiology Pyramidal Cells - cytology Pyramidal Cells - metabolism Rats Signal Transduction - physiology Subcellular Fractions - metabolism Synapses - metabolism |
title | Gamma-protocadherins are targeted to subsets of synapses and intracellular organelles in neurons |
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