Alignment of EphA4 and ephrin‐B2 expression patterns with developing modularity in the lateral cortex of the inferior colliculus
In the multimodal lateral cortex of the inferior colliculus (LCIC), there are two neurochemically and connectionally distinct compartments, termed modular and extramodular zones. Modular fields span LCIC layer 2 and are recipients of somatosensory afferents, while encompassing extramodular domains r...
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description | In the multimodal lateral cortex of the inferior colliculus (LCIC), there are two neurochemically and connectionally distinct compartments, termed modular and extramodular zones. Modular fields span LCIC layer 2 and are recipients of somatosensory afferents, while encompassing extramodular domains receive auditory inputs. Recently, in developing mice, we identified several markers (among them glutamic acid decarboxylase, GAD) that consistently label the same modular set, and a reliable extramodular marker, calretinin, (CR). Previous reports from our lab show similar modular–extramodular patterns for certain Eph–ephrin guidance members, although their precise alignment with the developing LCIC neurochemical framework has yet to be addressed. Here we confirm in the nascent LCIC complementary GAD/CR‐positive compartments, and characterize the registry of EphA4 and ephrin‐B2 expression patterns with respect to its emerging modular–extramodular organization. Immunocytochemical approaches in GAD67‐GFP knock‐in mice reveal patchy EphA4 and ephrin‐B2 domains that precisely align with GAD‐positive LCIC modules, and are complementary to CR‐defined extramodular zones. Such patterning was detectable neonatally, yielding discrete compartments prior to hearing onset. A dense plexus of EphA4‐positive fibers filled modules, surrounding labeled ephrin‐B2 and GAD cell populations. The majority of observed GABAergic neurons within modular boundaries were also positive for ephrin‐B2. These results suggest an early compartmentalization of the LCIC that is likely instructed in part through Eph–ephrin guidance mechanisms. The overlap of developing LCIC neurochemical and guidance patterns is discussed in the context of its seemingly segregated multimodal input–output streams.
Multiple‐labeling immunocytochemical experiments in the lateral cortex of the inferior colliculus in GAD67‐GFP mice reveal patchy EphA4 and ephrin‐B2 expression that overlaps with its modular–extramodular neurochemical compartments. This registry is apparent at birth and throughout the early postnatal period, providing a framework for its multimodal input–output arrays. |
doi_str_mv | 10.1002/cne.24525 |
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Multiple‐labeling immunocytochemical experiments in the lateral cortex of the inferior colliculus in GAD67‐GFP mice reveal patchy EphA4 and ephrin‐B2 expression that overlaps with its modular–extramodular neurochemical compartments. This registry is apparent at birth and throughout the early postnatal period, providing a framework for its multimodal input–output arrays.</description><identifier>ISSN: 0021-9967</identifier><identifier>EISSN: 1096-9861</identifier><identifier>DOI: 10.1002/cne.24525</identifier><identifier>PMID: 30156295</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley & Sons, Inc</publisher><subject>Animals ; Auditory Pathways - cytology ; Auditory Pathways - growth & development ; Auditory Pathways - metabolism ; Calretinin ; Eph ; EphA4 protein ; ephrin ; Ephrin-B2 - analysis ; Ephrin-B2 - biosynthesis ; Female ; Glutamate decarboxylase ; Glutamic acid ; guidance ; immunocytochemistry ; Inferior Colliculi - cytology ; Inferior Colliculi - growth & development ; Inferior Colliculi - metabolism ; Inferior colliculus ; Male ; Mice ; Mice, Inbred C57BL ; modularity ; multimodal ; Neurogenesis - physiology ; Neurons - cytology ; Neurons - metabolism ; patch‐matrix ; Receptor, EphA4 - analysis ; Receptor, EphA4 - biosynthesis ; RRID: AB_2619710 ; RRID:AB_2095679 ; RRID:AB_2095700 ; RRID:AB_2099371 ; RRID:AB_2278725 ; Sensory neurons ; Somatosensory cortex ; Somatosensory system ; γ-Aminobutyric acid</subject><ispartof>Journal of comparative neurology (1911), 2018-11, Vol.526 (16), p.2706-2721</ispartof><rights>2018 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4435-271d01a1f8fc590a86e9b61be746d3302acb5f30d822e734d1b7a0c305820cb43</citedby><cites>FETCH-LOGICAL-c4435-271d01a1f8fc590a86e9b61be746d3302acb5f30d822e734d1b7a0c305820cb43</cites><orcidid>0000-0003-1035-4104</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fcne.24525$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fcne.24525$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,780,784,885,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30156295$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gay, Sean M.</creatorcontrib><creatorcontrib>Brett, Cooper A.</creatorcontrib><creatorcontrib>Stinson, Jeremiah P.C.</creatorcontrib><creatorcontrib>Gabriele, Mark L.</creatorcontrib><title>Alignment of EphA4 and ephrin‐B2 expression patterns with developing modularity in the lateral cortex of the inferior colliculus</title><title>Journal of comparative neurology (1911)</title><addtitle>J Comp Neurol</addtitle><description>In the multimodal lateral cortex of the inferior colliculus (LCIC), there are two neurochemically and connectionally distinct compartments, termed modular and extramodular zones. Modular fields span LCIC layer 2 and are recipients of somatosensory afferents, while encompassing extramodular domains receive auditory inputs. Recently, in developing mice, we identified several markers (among them glutamic acid decarboxylase, GAD) that consistently label the same modular set, and a reliable extramodular marker, calretinin, (CR). Previous reports from our lab show similar modular–extramodular patterns for certain Eph–ephrin guidance members, although their precise alignment with the developing LCIC neurochemical framework has yet to be addressed. Here we confirm in the nascent LCIC complementary GAD/CR‐positive compartments, and characterize the registry of EphA4 and ephrin‐B2 expression patterns with respect to its emerging modular–extramodular organization. Immunocytochemical approaches in GAD67‐GFP knock‐in mice reveal patchy EphA4 and ephrin‐B2 domains that precisely align with GAD‐positive LCIC modules, and are complementary to CR‐defined extramodular zones. Such patterning was detectable neonatally, yielding discrete compartments prior to hearing onset. A dense plexus of EphA4‐positive fibers filled modules, surrounding labeled ephrin‐B2 and GAD cell populations. The majority of observed GABAergic neurons within modular boundaries were also positive for ephrin‐B2. These results suggest an early compartmentalization of the LCIC that is likely instructed in part through Eph–ephrin guidance mechanisms. The overlap of developing LCIC neurochemical and guidance patterns is discussed in the context of its seemingly segregated multimodal input–output streams.
Multiple‐labeling immunocytochemical experiments in the lateral cortex of the inferior colliculus in GAD67‐GFP mice reveal patchy EphA4 and ephrin‐B2 expression that overlaps with its modular–extramodular neurochemical compartments. This registry is apparent at birth and throughout the early postnatal period, providing a framework for its multimodal input–output arrays.</description><subject>Animals</subject><subject>Auditory Pathways - cytology</subject><subject>Auditory Pathways - growth & development</subject><subject>Auditory Pathways - metabolism</subject><subject>Calretinin</subject><subject>Eph</subject><subject>EphA4 protein</subject><subject>ephrin</subject><subject>Ephrin-B2 - analysis</subject><subject>Ephrin-B2 - biosynthesis</subject><subject>Female</subject><subject>Glutamate decarboxylase</subject><subject>Glutamic acid</subject><subject>guidance</subject><subject>immunocytochemistry</subject><subject>Inferior Colliculi - cytology</subject><subject>Inferior Colliculi - growth & development</subject><subject>Inferior Colliculi - metabolism</subject><subject>Inferior colliculus</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>modularity</subject><subject>multimodal</subject><subject>Neurogenesis - physiology</subject><subject>Neurons - cytology</subject><subject>Neurons - metabolism</subject><subject>patch‐matrix</subject><subject>Receptor, EphA4 - analysis</subject><subject>Receptor, EphA4 - biosynthesis</subject><subject>RRID: AB_2619710</subject><subject>RRID:AB_2095679</subject><subject>RRID:AB_2095700</subject><subject>RRID:AB_2099371</subject><subject>RRID:AB_2278725</subject><subject>Sensory neurons</subject><subject>Somatosensory cortex</subject><subject>Somatosensory system</subject><subject>γ-Aminobutyric acid</subject><issn>0021-9967</issn><issn>1096-9861</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kctu1DAUhiMEokNhwQsgS2xgkdaX2Ik3SMNouEgVbGBtOc7JxJVjBztpOzvEE_CMPAkeplSAxMrSOZ8-_cd_UTwl-IxgTM-NhzNaccrvFSuCpShlI8j9YpV3pJRS1CfFo5QuMcZSsuZhccIw4YJKviq-rZ3d-RH8jEKPttOwrpD2HYJpiNb_-Pr9NUVwM0VIyQaPJj3PEH1C13YeUAdX4MJk_Q6NoVucjnbeI-vRPAByOpPaIRPiDDcH-2FqfQ_RhpjHzlmzuCU9Lh702iV4cvueFp_fbD9t3pUXH9--36wvSlNVjJe0Jh0mmvRNb7jEuhEgW0FaqCvRMYapNi3vGe4aSqFmVUfaWmPDMG8oNm3FTotXR--0tCN0Jt-c86kp2lHHvQraqr833g5qF66UqIjgRGbBi1tBDF8WSLMabTLgnPYQlqRo_nrOqajqjD7_B70MS_T5PEUJqyiRuBGZenmkTAwpRejvwhCsDs2q3Kz61Wxmn_2Z_o78XWUGzo_AtXWw_79JbT5sj8qfQYywJw</recordid><startdate>20181101</startdate><enddate>20181101</enddate><creator>Gay, Sean M.</creator><creator>Brett, Cooper A.</creator><creator>Stinson, Jeremiah P.C.</creator><creator>Gabriele, Mark L.</creator><general>John Wiley & Sons, Inc</general><general>Wiley Subscription Services, Inc</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>7QR</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-1035-4104</orcidid></search><sort><creationdate>20181101</creationdate><title>Alignment of EphA4 and ephrin‐B2 expression patterns with developing modularity in the lateral cortex of the inferior colliculus</title><author>Gay, Sean M. ; Brett, Cooper A. ; Stinson, Jeremiah P.C. ; Gabriele, Mark L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4435-271d01a1f8fc590a86e9b61be746d3302acb5f30d822e734d1b7a0c305820cb43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Animals</topic><topic>Auditory Pathways - cytology</topic><topic>Auditory Pathways - growth & development</topic><topic>Auditory Pathways - metabolism</topic><topic>Calretinin</topic><topic>Eph</topic><topic>EphA4 protein</topic><topic>ephrin</topic><topic>Ephrin-B2 - analysis</topic><topic>Ephrin-B2 - biosynthesis</topic><topic>Female</topic><topic>Glutamate decarboxylase</topic><topic>Glutamic acid</topic><topic>guidance</topic><topic>immunocytochemistry</topic><topic>Inferior Colliculi - cytology</topic><topic>Inferior Colliculi - growth & development</topic><topic>Inferior Colliculi - metabolism</topic><topic>Inferior colliculus</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>modularity</topic><topic>multimodal</topic><topic>Neurogenesis - physiology</topic><topic>Neurons - cytology</topic><topic>Neurons - metabolism</topic><topic>patch‐matrix</topic><topic>Receptor, EphA4 - analysis</topic><topic>Receptor, EphA4 - biosynthesis</topic><topic>RRID: AB_2619710</topic><topic>RRID:AB_2095679</topic><topic>RRID:AB_2095700</topic><topic>RRID:AB_2099371</topic><topic>RRID:AB_2278725</topic><topic>Sensory neurons</topic><topic>Somatosensory cortex</topic><topic>Somatosensory system</topic><topic>γ-Aminobutyric acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gay, Sean M.</creatorcontrib><creatorcontrib>Brett, Cooper A.</creatorcontrib><creatorcontrib>Stinson, Jeremiah P.C.</creatorcontrib><creatorcontrib>Gabriele, Mark L.</creatorcontrib><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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of comparative neurology (1911)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gay, Sean M.</au><au>Brett, Cooper A.</au><au>Stinson, Jeremiah P.C.</au><au>Gabriele, Mark L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Alignment of EphA4 and ephrin‐B2 expression patterns with developing modularity in the lateral cortex of the inferior colliculus</atitle><jtitle>Journal of comparative neurology (1911)</jtitle><addtitle>J Comp Neurol</addtitle><date>2018-11-01</date><risdate>2018</risdate><volume>526</volume><issue>16</issue><spage>2706</spage><epage>2721</epage><pages>2706-2721</pages><issn>0021-9967</issn><eissn>1096-9861</eissn><abstract>In the multimodal lateral cortex of the inferior colliculus (LCIC), there are two neurochemically and connectionally distinct compartments, termed modular and extramodular zones. Modular fields span LCIC layer 2 and are recipients of somatosensory afferents, while encompassing extramodular domains receive auditory inputs. Recently, in developing mice, we identified several markers (among them glutamic acid decarboxylase, GAD) that consistently label the same modular set, and a reliable extramodular marker, calretinin, (CR). Previous reports from our lab show similar modular–extramodular patterns for certain Eph–ephrin guidance members, although their precise alignment with the developing LCIC neurochemical framework has yet to be addressed. Here we confirm in the nascent LCIC complementary GAD/CR‐positive compartments, and characterize the registry of EphA4 and ephrin‐B2 expression patterns with respect to its emerging modular–extramodular organization. Immunocytochemical approaches in GAD67‐GFP knock‐in mice reveal patchy EphA4 and ephrin‐B2 domains that precisely align with GAD‐positive LCIC modules, and are complementary to CR‐defined extramodular zones. Such patterning was detectable neonatally, yielding discrete compartments prior to hearing onset. A dense plexus of EphA4‐positive fibers filled modules, surrounding labeled ephrin‐B2 and GAD cell populations. The majority of observed GABAergic neurons within modular boundaries were also positive for ephrin‐B2. These results suggest an early compartmentalization of the LCIC that is likely instructed in part through Eph–ephrin guidance mechanisms. The overlap of developing LCIC neurochemical and guidance patterns is discussed in the context of its seemingly segregated multimodal input–output streams.
Multiple‐labeling immunocytochemical experiments in the lateral cortex of the inferior colliculus in GAD67‐GFP mice reveal patchy EphA4 and ephrin‐B2 expression that overlaps with its modular–extramodular neurochemical compartments. This registry is apparent at birth and throughout the early postnatal period, providing a framework for its multimodal input–output arrays.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><pmid>30156295</pmid><doi>10.1002/cne.24525</doi><tpages>16</tpages><orcidid>https://orcid.org/0000-0003-1035-4104</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Animals Auditory Pathways - cytology Auditory Pathways - growth & development Auditory Pathways - metabolism Calretinin Eph EphA4 protein ephrin Ephrin-B2 - analysis Ephrin-B2 - biosynthesis Female Glutamate decarboxylase Glutamic acid guidance immunocytochemistry Inferior Colliculi - cytology Inferior Colliculi - growth & development Inferior Colliculi - metabolism Inferior colliculus Male Mice Mice, Inbred C57BL modularity multimodal Neurogenesis - physiology Neurons - cytology Neurons - metabolism patch‐matrix Receptor, EphA4 - analysis Receptor, EphA4 - biosynthesis RRID: AB_2619710 RRID:AB_2095679 RRID:AB_2095700 RRID:AB_2099371 RRID:AB_2278725 Sensory neurons Somatosensory cortex Somatosensory system γ-Aminobutyric acid |
title | Alignment of EphA4 and ephrin‐B2 expression patterns with developing modularity in the lateral cortex of the inferior colliculus |
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