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EphA7 expression identifies a unique neuronal compartment in the rat striatum
Prior studies have identified two anatomically and neurochemically distinct cellular compartments within the mammalian striatum, termed striosomes and matrix, which express μ‐opioid receptors (μOR) and EphA4, respectively. Here we identify and characterize an additional compartment in the rat striat...
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Published in: | Journal of comparative neurology (1911) 2013-08, Vol.521 (12), p.2663-2679 |
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description | Prior studies have identified two anatomically and neurochemically distinct cellular compartments within the mammalian striatum, termed striosomes and matrix, which express μ‐opioid receptors (μOR) and EphA4, respectively. Here we identify and characterize an additional compartment in the rat striatum composed of neurons that express EphA7. In situ hybridization and immunohistochemical data indicate that neurons expressing EphA7 mRNA and protein are arranged in a banded “matrisome‐like” pattern confined to the matrix in the dorsal striatum. Within the ventral striatum, EphA7‐positive (+) neurons have a less organized mosaic pattern that partially overlaps areas expressing μOR. Immunolabeling data demonstrate that EphA7+ striatofugal axons form distinct fascicles leaving the striatum. Within the globus pallidus, EphA7+ axons terminate primarily within ventromedial areas of the nucleus and along its striatal border. EphA7+ axons avoid regions containing dopamine neurons within the substantia nigra and preferentially innervate areas near the rostral and caudal margins of the nucleus. Within both nuclei, EphA7+ axons have similar but more restricted terminal fields than the entire population of EphA4+ matrix axons, indicating that EphA7+ axons comprise a subpopulation of matrix axons. Ligand binding data demonstrate that ephrin‐A5 selectively binds areas of the striatum, globus pallidus, and substantia nigra containing EphA7+ neurons and axons, but not areas expressing only EphA4. Our findings demonstrate that EphA7 expression identifies a novel “matrisome” compartment within the matrix that binds ephrin‐A5 and possesses unique axonal projections. Our findings also suggest that EphA7 and ephrin‐A5 may participate in the formation of this matrisome subcompartment and its striatofugal projections. J. Comp. Neurol. 521:2663–2679, 2013. © 2013 Wiley Periodicals, Inc.
The EphA7 receptor is a member of the Eph/ephrin family of molecules, which are known to participate in axonal guidance and cell boundary formation during development. In the postnatal striatum, EphA7 expression delineates a novel striatal compartment. These “matrisome” compartments are located entirely within the striatal matrix and are organized into bands paralleling the curvature of the external capsule. The postnatal expression pattern of EphA7 suggests it plays a role in striatal compartment formation and/or the formation of striatal connections. |
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The EphA7 receptor is a member of the Eph/ephrin family of molecules, which are known to participate in axonal guidance and cell boundary formation during development. In the postnatal striatum, EphA7 expression delineates a novel striatal compartment. These “matrisome” compartments are located entirely within the striatal matrix and are organized into bands paralleling the curvature of the external capsule. The postnatal expression pattern of EphA7 suggests it plays a role in striatal compartment formation and/or the formation of striatal connections.</description><identifier>ISSN: 0021-9967</identifier><identifier>EISSN: 1096-9861</identifier><identifier>DOI: 10.1002/cne.23308</identifier><identifier>PMID: 23348681</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>anatomy ; Animals ; Animals, Newborn ; Axon guidance ; Axons - metabolism ; basal ganglia ; Corpus Striatum - cytology ; Corpus Striatum - metabolism ; ephrin ; Female ; Male ; matrisome ; matrix ; Neural Pathways - physiology ; Neurons - cytology ; Neurons - metabolism ; Pregnancy ; Rats ; Rats, Sprague-Dawley ; Receptor, EphA5 - metabolism ; Receptor, EphA7 - genetics ; Receptor, EphA7 - metabolism ; Receptors, Opioid, mu - genetics ; Receptors, Opioid, mu - metabolism ; RNA, Messenger - metabolism ; striosomes ; Tyrosine 3-Monooxygenase - metabolism</subject><ispartof>Journal of comparative neurology (1911), 2013-08, Vol.521 (12), p.2663-2679</ispartof><rights>Copyright © 2013 Wiley Periodicals, Inc., A Wiley Company</rights><rights>Copyright © 2013 Wiley Periodicals, Inc., A Wiley Company.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4908-a8c2adec2df1b6998102dad55dbfbff1e7f49c154d23aad2061ad74aad8380083</citedby><cites>FETCH-LOGICAL-c4908-a8c2adec2df1b6998102dad55dbfbff1e7f49c154d23aad2061ad74aad8380083</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23348681$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tai, Alexander X.</creatorcontrib><creatorcontrib>Cassidy, Robert M.</creatorcontrib><creatorcontrib>Kromer, Lawrence F.</creatorcontrib><title>EphA7 expression identifies a unique neuronal compartment in the rat striatum</title><title>Journal of comparative neurology (1911)</title><addtitle>J. Comp. Neurol</addtitle><description>Prior studies have identified two anatomically and neurochemically distinct cellular compartments within the mammalian striatum, termed striosomes and matrix, which express μ‐opioid receptors (μOR) and EphA4, respectively. Here we identify and characterize an additional compartment in the rat striatum composed of neurons that express EphA7. In situ hybridization and immunohistochemical data indicate that neurons expressing EphA7 mRNA and protein are arranged in a banded “matrisome‐like” pattern confined to the matrix in the dorsal striatum. Within the ventral striatum, EphA7‐positive (+) neurons have a less organized mosaic pattern that partially overlaps areas expressing μOR. Immunolabeling data demonstrate that EphA7+ striatofugal axons form distinct fascicles leaving the striatum. Within the globus pallidus, EphA7+ axons terminate primarily within ventromedial areas of the nucleus and along its striatal border. EphA7+ axons avoid regions containing dopamine neurons within the substantia nigra and preferentially innervate areas near the rostral and caudal margins of the nucleus. Within both nuclei, EphA7+ axons have similar but more restricted terminal fields than the entire population of EphA4+ matrix axons, indicating that EphA7+ axons comprise a subpopulation of matrix axons. Ligand binding data demonstrate that ephrin‐A5 selectively binds areas of the striatum, globus pallidus, and substantia nigra containing EphA7+ neurons and axons, but not areas expressing only EphA4. Our findings demonstrate that EphA7 expression identifies a novel “matrisome” compartment within the matrix that binds ephrin‐A5 and possesses unique axonal projections. Our findings also suggest that EphA7 and ephrin‐A5 may participate in the formation of this matrisome subcompartment and its striatofugal projections. J. Comp. Neurol. 521:2663–2679, 2013. © 2013 Wiley Periodicals, Inc.
The EphA7 receptor is a member of the Eph/ephrin family of molecules, which are known to participate in axonal guidance and cell boundary formation during development. In the postnatal striatum, EphA7 expression delineates a novel striatal compartment. These “matrisome” compartments are located entirely within the striatal matrix and are organized into bands paralleling the curvature of the external capsule. The postnatal expression pattern of EphA7 suggests it plays a role in striatal compartment formation and/or the formation of striatal connections.</description><subject>anatomy</subject><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Axon guidance</subject><subject>Axons - metabolism</subject><subject>basal ganglia</subject><subject>Corpus Striatum - cytology</subject><subject>Corpus Striatum - metabolism</subject><subject>ephrin</subject><subject>Female</subject><subject>Male</subject><subject>matrisome</subject><subject>matrix</subject><subject>Neural Pathways - physiology</subject><subject>Neurons - cytology</subject><subject>Neurons - metabolism</subject><subject>Pregnancy</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptor, EphA5 - metabolism</subject><subject>Receptor, EphA7 - genetics</subject><subject>Receptor, EphA7 - metabolism</subject><subject>Receptors, Opioid, mu - genetics</subject><subject>Receptors, Opioid, mu - metabolism</subject><subject>RNA, Messenger - metabolism</subject><subject>striosomes</subject><subject>Tyrosine 3-Monooxygenase - metabolism</subject><issn>0021-9967</issn><issn>1096-9861</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqN0U1rFDEYB_BQFLtWD_0CEvCih2mfJ5nJy7Fd1iqsWyhajyE7ydDUeWsyg9tvb-q2PQiCpwTye_4k-RNyjHCCAOy07v0J4xzUAVkgaFFoJfAFWeQzLLQW8pC8TukWALTm6hU5zLhUQuGCfF2NN2eS-t0YfUph6Glwvp9CE3yils59uJs97f0ch962tB660capy4SGnk43nkY70TTFYKe5e0NeNrZN_u3jekS-f1p9W34u1pcXX5Zn66IuNajCqppZ52vmGtwKrRUCc9ZVlds226ZBL5tS11iVjnFrHQOB1skybxVXAIofkQ_73DEO-X5pMl1ItW9b2_thTgZLXgJK0P9BuQRkAniZ6fu_6O0wx_zsByU0clYBZvVxr-o4pBR9Y8YYOhvvDYJ5qMPkOsyfOrJ995g4bzvvnuXT_2dwuge_Quvv_51klpvVU2Sxnwhp8rvnCRt_GiG5rMyPzYW5UtfyerM-N0v-GztUonk</recordid><startdate>20130815</startdate><enddate>20130815</enddate><creator>Tai, Alexander X.</creator><creator>Cassidy, Robert M.</creator><creator>Kromer, Lawrence F.</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</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>7QR</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20130815</creationdate><title>EphA7 expression identifies a unique neuronal compartment in the rat striatum</title><author>Tai, Alexander X. ; Cassidy, Robert M. ; Kromer, Lawrence F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4908-a8c2adec2df1b6998102dad55dbfbff1e7f49c154d23aad2061ad74aad8380083</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>anatomy</topic><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Axon guidance</topic><topic>Axons - metabolism</topic><topic>basal ganglia</topic><topic>Corpus Striatum - cytology</topic><topic>Corpus Striatum - metabolism</topic><topic>ephrin</topic><topic>Female</topic><topic>Male</topic><topic>matrisome</topic><topic>matrix</topic><topic>Neural Pathways - physiology</topic><topic>Neurons - cytology</topic><topic>Neurons - metabolism</topic><topic>Pregnancy</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptor, EphA5 - metabolism</topic><topic>Receptor, EphA7 - genetics</topic><topic>Receptor, EphA7 - metabolism</topic><topic>Receptors, Opioid, mu - genetics</topic><topic>Receptors, Opioid, mu - metabolism</topic><topic>RNA, Messenger - metabolism</topic><topic>striosomes</topic><topic>Tyrosine 3-Monooxygenase - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tai, Alexander X.</creatorcontrib><creatorcontrib>Cassidy, Robert M.</creatorcontrib><creatorcontrib>Kromer, Lawrence F.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of comparative neurology (1911)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tai, Alexander X.</au><au>Cassidy, Robert M.</au><au>Kromer, Lawrence F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>EphA7 expression identifies a unique neuronal compartment in the rat striatum</atitle><jtitle>Journal of comparative neurology (1911)</jtitle><addtitle>J. Comp. Neurol</addtitle><date>2013-08-15</date><risdate>2013</risdate><volume>521</volume><issue>12</issue><spage>2663</spage><epage>2679</epage><pages>2663-2679</pages><issn>0021-9967</issn><eissn>1096-9861</eissn><abstract>Prior studies have identified two anatomically and neurochemically distinct cellular compartments within the mammalian striatum, termed striosomes and matrix, which express μ‐opioid receptors (μOR) and EphA4, respectively. Here we identify and characterize an additional compartment in the rat striatum composed of neurons that express EphA7. In situ hybridization and immunohistochemical data indicate that neurons expressing EphA7 mRNA and protein are arranged in a banded “matrisome‐like” pattern confined to the matrix in the dorsal striatum. Within the ventral striatum, EphA7‐positive (+) neurons have a less organized mosaic pattern that partially overlaps areas expressing μOR. Immunolabeling data demonstrate that EphA7+ striatofugal axons form distinct fascicles leaving the striatum. Within the globus pallidus, EphA7+ axons terminate primarily within ventromedial areas of the nucleus and along its striatal border. EphA7+ axons avoid regions containing dopamine neurons within the substantia nigra and preferentially innervate areas near the rostral and caudal margins of the nucleus. Within both nuclei, EphA7+ axons have similar but more restricted terminal fields than the entire population of EphA4+ matrix axons, indicating that EphA7+ axons comprise a subpopulation of matrix axons. Ligand binding data demonstrate that ephrin‐A5 selectively binds areas of the striatum, globus pallidus, and substantia nigra containing EphA7+ neurons and axons, but not areas expressing only EphA4. Our findings demonstrate that EphA7 expression identifies a novel “matrisome” compartment within the matrix that binds ephrin‐A5 and possesses unique axonal projections. Our findings also suggest that EphA7 and ephrin‐A5 may participate in the formation of this matrisome subcompartment and its striatofugal projections. J. Comp. Neurol. 521:2663–2679, 2013. © 2013 Wiley Periodicals, Inc.
The EphA7 receptor is a member of the Eph/ephrin family of molecules, which are known to participate in axonal guidance and cell boundary formation during development. In the postnatal striatum, EphA7 expression delineates a novel striatal compartment. These “matrisome” compartments are located entirely within the striatal matrix and are organized into bands paralleling the curvature of the external capsule. The postnatal expression pattern of EphA7 suggests it plays a role in striatal compartment formation and/or the formation of striatal connections.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>23348681</pmid><doi>10.1002/cne.23308</doi><tpages>17</tpages></addata></record> |
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subjects | anatomy Animals Animals, Newborn Axon guidance Axons - metabolism basal ganglia Corpus Striatum - cytology Corpus Striatum - metabolism ephrin Female Male matrisome matrix Neural Pathways - physiology Neurons - cytology Neurons - metabolism Pregnancy Rats Rats, Sprague-Dawley Receptor, EphA5 - metabolism Receptor, EphA7 - genetics Receptor, EphA7 - metabolism Receptors, Opioid, mu - genetics Receptors, Opioid, mu - metabolism RNA, Messenger - metabolism striosomes Tyrosine 3-Monooxygenase - metabolism |
title | EphA7 expression identifies a unique neuronal compartment in the rat striatum |
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