Cerebellar modules in the olivo‐cortico‐nuclear loop demarcated by pcdh10 expression in the adult mouse
Topographic connection between corresponding compartments of the cerebellar cortex, cerebellar nuclei, and inferior olive form parallel modules, which are essential for the cerebellar function. Compared to the striped cortical compartmentalization which are labeled by molecular markers, such as aldo...
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description | Topographic connection between corresponding compartments of the cerebellar cortex, cerebellar nuclei, and inferior olive form parallel modules, which are essential for the cerebellar function. Compared to the striped cortical compartmentalization which are labeled by molecular markers, such as aldolase C (Aldoc) or zebrin II, the presumed corresponding organization of the cerebellar nuclei and inferior olivary nucleus has not been much clarified. We focused on the expression pattern of pcdh10 gene coding cell adhesion molecule protocadherin 10 (Pcdh10) in adult mice. In the cortex, pcdh10 was strongly expressed in (a) Aldoc‐positive vermal stripes a+//2+ in lobules VI–VII, (b) paravermal narrow stripes c+, d+, 4b+, 5a+ in crus I and neighboring lobules, and (c) paravermal stripes 4+//5+ across all lobules from lobule III to paraflocculus. In the cerebellar nuclei, pcdh10 was expressed strongly in the caudal part of the medial nucleus and the lateral part of the posterior interposed nucleus which project less to the medulla or to the red nucleus than to other metencephalic, mesencephalic, and diencephalic areas. In the inferior olive, pcdh10 was expressed strongly in the rostral and medioventrocaudal parts of the medial accessory olive which has connection with the mesencephalic areas rather than the spinal cord. Olivocerebellar and corticonuclear axonal labeling confirmed that the three cortical pcdh10‐positive areas were topographically connected to the nuclear and olivary pcdh10‐positive areas, demonstrating their coincidence with modular structures in the olivo‐cortico‐nuclear loop. We speculate that some of these modules are functionally involved in various nonsomatosensorimotor tasks via their afferent and efferent connections.
Pcdh10 was expressed in particular Aldoc‐positive stripes in the cerebellar cortex (center), and in particular areas in the cerebellar nuclei (top) and inferior olive (bottom). These pcdh10‐positive areas were topographically connected (arrows) to form cerebellar modules, some of which may be involved in nonsomatosensorimotor function. |
doi_str_mv | 10.1002/cne.24499 |
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Pcdh10 was expressed in particular Aldoc‐positive stripes in the cerebellar cortex (center), and in particular areas in the cerebellar nuclei (top) and inferior olive (bottom). These pcdh10‐positive areas were topographically connected (arrows) to form cerebellar modules, some of which may be involved in nonsomatosensorimotor function.</description><identifier>ISSN: 0021-9967</identifier><identifier>EISSN: 1096-9861</identifier><identifier>DOI: 10.1002/cne.24499</identifier><identifier>PMID: 30004589</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley & Sons, Inc</publisher><subject><![CDATA[Animals ; Cadherins - genetics ; Cadherins - metabolism ; Cell adhesion & migration ; cell adhesion molecule ; Cell adhesion molecules ; cerebellar cortex ; Cerebellar Cortex - anatomy & histology ; Cerebellar Cortex - metabolism ; cerebellar nuclei ; Cerebellar Nuclei - anatomy & histology ; Cerebellar Nuclei - metabolism ; Cerebellum ; Cerebral Cortex - anatomy & histology ; Cerebral Cortex - metabolism ; Cortex ; Immunohistochemistry ; Inferior olivary nucleus ; inferior olive ; Male ; Medulla oblongata ; Mice ; Mice, Inbred C57BL ; Neural Pathways - anatomy & histology ; Neural Pathways - metabolism ; Olivary Nucleus - anatomy & histology ; Olivary Nucleus - metabolism ; Phenotype ; Protocadherin ; Purkinje Cells - physiology ; Red nucleus ; RRID:AB_2017112 ; RRID:AB_2313920 ; Sensory neurons ; Spinal cord ; Zebrin II]]></subject><ispartof>Journal of comparative neurology (1911), 2018-10, Vol.526 (15), p.2406-2427</ispartof><rights>2018 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5039-6952d93b0b5cbac0514bee2af8f40ba3b74047415fca4cf2cd9e7866c595e73c3</citedby><cites>FETCH-LOGICAL-c5039-6952d93b0b5cbac0514bee2af8f40ba3b74047415fca4cf2cd9e7866c595e73c3</cites><orcidid>0000-0002-1397-0669 ; 0000-0002-4598-9882 ; 0000-0001-9630-2756</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.24499$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fcne.24499$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30004589$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sarpong, Gideon A.</creatorcontrib><creatorcontrib>Vibulyaseck, Suteera</creatorcontrib><creatorcontrib>Luo, Yuanjun</creatorcontrib><creatorcontrib>Biswas, Mohammad S.</creatorcontrib><creatorcontrib>Fujita, Hirofumi</creatorcontrib><creatorcontrib>Hirano, Shinji</creatorcontrib><creatorcontrib>Sugihara, Izumi</creatorcontrib><title>Cerebellar modules in the olivo‐cortico‐nuclear loop demarcated by pcdh10 expression in the adult mouse</title><title>Journal of comparative neurology (1911)</title><addtitle>J Comp Neurol</addtitle><description>Topographic connection between corresponding compartments of the cerebellar cortex, cerebellar nuclei, and inferior olive form parallel modules, which are essential for the cerebellar function. Compared to the striped cortical compartmentalization which are labeled by molecular markers, such as aldolase C (Aldoc) or zebrin II, the presumed corresponding organization of the cerebellar nuclei and inferior olivary nucleus has not been much clarified. We focused on the expression pattern of pcdh10 gene coding cell adhesion molecule protocadherin 10 (Pcdh10) in adult mice. In the cortex, pcdh10 was strongly expressed in (a) Aldoc‐positive vermal stripes a+//2+ in lobules VI–VII, (b) paravermal narrow stripes c+, d+, 4b+, 5a+ in crus I and neighboring lobules, and (c) paravermal stripes 4+//5+ across all lobules from lobule III to paraflocculus. In the cerebellar nuclei, pcdh10 was expressed strongly in the caudal part of the medial nucleus and the lateral part of the posterior interposed nucleus which project less to the medulla or to the red nucleus than to other metencephalic, mesencephalic, and diencephalic areas. In the inferior olive, pcdh10 was expressed strongly in the rostral and medioventrocaudal parts of the medial accessory olive which has connection with the mesencephalic areas rather than the spinal cord. Olivocerebellar and corticonuclear axonal labeling confirmed that the three cortical pcdh10‐positive areas were topographically connected to the nuclear and olivary pcdh10‐positive areas, demonstrating their coincidence with modular structures in the olivo‐cortico‐nuclear loop. We speculate that some of these modules are functionally involved in various nonsomatosensorimotor tasks via their afferent and efferent connections.
Pcdh10 was expressed in particular Aldoc‐positive stripes in the cerebellar cortex (center), and in particular areas in the cerebellar nuclei (top) and inferior olive (bottom). These pcdh10‐positive areas were topographically connected (arrows) to form cerebellar modules, some of which may be involved in nonsomatosensorimotor function.</description><subject>Animals</subject><subject>Cadherins - genetics</subject><subject>Cadherins - metabolism</subject><subject>Cell adhesion & migration</subject><subject>cell adhesion molecule</subject><subject>Cell adhesion molecules</subject><subject>cerebellar cortex</subject><subject>Cerebellar Cortex - anatomy & histology</subject><subject>Cerebellar Cortex - metabolism</subject><subject>cerebellar nuclei</subject><subject>Cerebellar Nuclei - anatomy & histology</subject><subject>Cerebellar Nuclei - metabolism</subject><subject>Cerebellum</subject><subject>Cerebral Cortex - anatomy & histology</subject><subject>Cerebral Cortex - metabolism</subject><subject>Cortex</subject><subject>Immunohistochemistry</subject><subject>Inferior olivary nucleus</subject><subject>inferior olive</subject><subject>Male</subject><subject>Medulla oblongata</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Neural Pathways - anatomy & histology</subject><subject>Neural Pathways - metabolism</subject><subject>Olivary Nucleus - anatomy & histology</subject><subject>Olivary Nucleus - metabolism</subject><subject>Phenotype</subject><subject>Protocadherin</subject><subject>Purkinje Cells - physiology</subject><subject>Red nucleus</subject><subject>RRID:AB_2017112</subject><subject>RRID:AB_2313920</subject><subject>Sensory neurons</subject><subject>Spinal cord</subject><subject>Zebrin II</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>eNp1kc1O3DAQx62qqLt8HHgBFIlLOWQZfyXxEa0oICG4tGfLdiYiSzYOdtJ2b32EPiNPUm-X7QGppxlpfvppZv6EnFJYUAB26XpcMCGU-kDmFFSRq6qgH8k8zWiuVFHOyGGMKwBQilefyIynVshKzcnzEgNa7DoTsrWvpw5j1vbZ-ISZ79rv_vXXb-fD2Lpt10-uwwR23g9ZjWsTnBmxzuwmG1z9RCHDn0PAGFvf7y0mOcekniIek4PGdBFP3uoR-fbl-uvyNr9_vLlbXt3nTgJXeaEkqxW3YKWzxoGkwiIy01SNAGu4LQWIUlDZOCNcw1ytsKyKwkklseSOH5HPO-8Q_MuEcdTrNrrtjT2mPTSDEphgsoCEnr9DV34KfdpOM8q44MBLmqiLHeWCjzFgo4fQpus3moLeJqBTAvpvAok9ezNOdo31P3L_8gRc7oAfbYeb_5v08uF6p_wDPEKR_g</recordid><startdate>20181015</startdate><enddate>20181015</enddate><creator>Sarpong, Gideon A.</creator><creator>Vibulyaseck, Suteera</creator><creator>Luo, Yuanjun</creator><creator>Biswas, Mohammad S.</creator><creator>Fujita, Hirofumi</creator><creator>Hirano, Shinji</creator><creator>Sugihara, Izumi</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><orcidid>https://orcid.org/0000-0002-1397-0669</orcidid><orcidid>https://orcid.org/0000-0002-4598-9882</orcidid><orcidid>https://orcid.org/0000-0001-9630-2756</orcidid></search><sort><creationdate>20181015</creationdate><title>Cerebellar modules in the olivo‐cortico‐nuclear loop demarcated by pcdh10 expression in the adult mouse</title><author>Sarpong, Gideon A. ; Vibulyaseck, Suteera ; Luo, Yuanjun ; Biswas, Mohammad S. ; Fujita, Hirofumi ; Hirano, Shinji ; Sugihara, Izumi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5039-6952d93b0b5cbac0514bee2af8f40ba3b74047415fca4cf2cd9e7866c595e73c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Animals</topic><topic>Cadherins - genetics</topic><topic>Cadherins - metabolism</topic><topic>Cell adhesion & migration</topic><topic>cell adhesion molecule</topic><topic>Cell adhesion molecules</topic><topic>cerebellar cortex</topic><topic>Cerebellar Cortex - anatomy & histology</topic><topic>Cerebellar Cortex - metabolism</topic><topic>cerebellar nuclei</topic><topic>Cerebellar Nuclei - anatomy & histology</topic><topic>Cerebellar Nuclei - metabolism</topic><topic>Cerebellum</topic><topic>Cerebral Cortex - anatomy & histology</topic><topic>Cerebral Cortex - metabolism</topic><topic>Cortex</topic><topic>Immunohistochemistry</topic><topic>Inferior olivary nucleus</topic><topic>inferior olive</topic><topic>Male</topic><topic>Medulla oblongata</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Neural Pathways - anatomy & histology</topic><topic>Neural Pathways - metabolism</topic><topic>Olivary Nucleus - anatomy & histology</topic><topic>Olivary Nucleus - metabolism</topic><topic>Phenotype</topic><topic>Protocadherin</topic><topic>Purkinje Cells - physiology</topic><topic>Red nucleus</topic><topic>RRID:AB_2017112</topic><topic>RRID:AB_2313920</topic><topic>Sensory neurons</topic><topic>Spinal cord</topic><topic>Zebrin II</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sarpong, Gideon A.</creatorcontrib><creatorcontrib>Vibulyaseck, Suteera</creatorcontrib><creatorcontrib>Luo, Yuanjun</creatorcontrib><creatorcontrib>Biswas, Mohammad S.</creatorcontrib><creatorcontrib>Fujita, Hirofumi</creatorcontrib><creatorcontrib>Hirano, Shinji</creatorcontrib><creatorcontrib>Sugihara, Izumi</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><jtitle>Journal of comparative neurology (1911)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sarpong, Gideon A.</au><au>Vibulyaseck, Suteera</au><au>Luo, Yuanjun</au><au>Biswas, Mohammad S.</au><au>Fujita, Hirofumi</au><au>Hirano, Shinji</au><au>Sugihara, Izumi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cerebellar modules in the olivo‐cortico‐nuclear loop demarcated by pcdh10 expression in the adult mouse</atitle><jtitle>Journal of comparative neurology (1911)</jtitle><addtitle>J Comp Neurol</addtitle><date>2018-10-15</date><risdate>2018</risdate><volume>526</volume><issue>15</issue><spage>2406</spage><epage>2427</epage><pages>2406-2427</pages><issn>0021-9967</issn><eissn>1096-9861</eissn><abstract>Topographic connection between corresponding compartments of the cerebellar cortex, cerebellar nuclei, and inferior olive form parallel modules, which are essential for the cerebellar function. Compared to the striped cortical compartmentalization which are labeled by molecular markers, such as aldolase C (Aldoc) or zebrin II, the presumed corresponding organization of the cerebellar nuclei and inferior olivary nucleus has not been much clarified. We focused on the expression pattern of pcdh10 gene coding cell adhesion molecule protocadherin 10 (Pcdh10) in adult mice. In the cortex, pcdh10 was strongly expressed in (a) Aldoc‐positive vermal stripes a+//2+ in lobules VI–VII, (b) paravermal narrow stripes c+, d+, 4b+, 5a+ in crus I and neighboring lobules, and (c) paravermal stripes 4+//5+ across all lobules from lobule III to paraflocculus. In the cerebellar nuclei, pcdh10 was expressed strongly in the caudal part of the medial nucleus and the lateral part of the posterior interposed nucleus which project less to the medulla or to the red nucleus than to other metencephalic, mesencephalic, and diencephalic areas. In the inferior olive, pcdh10 was expressed strongly in the rostral and medioventrocaudal parts of the medial accessory olive which has connection with the mesencephalic areas rather than the spinal cord. Olivocerebellar and corticonuclear axonal labeling confirmed that the three cortical pcdh10‐positive areas were topographically connected to the nuclear and olivary pcdh10‐positive areas, demonstrating their coincidence with modular structures in the olivo‐cortico‐nuclear loop. We speculate that some of these modules are functionally involved in various nonsomatosensorimotor tasks via their afferent and efferent connections.
Pcdh10 was expressed in particular Aldoc‐positive stripes in the cerebellar cortex (center), and in particular areas in the cerebellar nuclei (top) and inferior olive (bottom). These pcdh10‐positive areas were topographically connected (arrows) to form cerebellar modules, some of which may be involved in nonsomatosensorimotor function.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><pmid>30004589</pmid><doi>10.1002/cne.24499</doi><tpages>22</tpages><orcidid>https://orcid.org/0000-0002-1397-0669</orcidid><orcidid>https://orcid.org/0000-0002-4598-9882</orcidid><orcidid>https://orcid.org/0000-0001-9630-2756</orcidid></addata></record> |
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subjects | Animals Cadherins - genetics Cadherins - metabolism Cell adhesion & migration cell adhesion molecule Cell adhesion molecules cerebellar cortex Cerebellar Cortex - anatomy & histology Cerebellar Cortex - metabolism cerebellar nuclei Cerebellar Nuclei - anatomy & histology Cerebellar Nuclei - metabolism Cerebellum Cerebral Cortex - anatomy & histology Cerebral Cortex - metabolism Cortex Immunohistochemistry Inferior olivary nucleus inferior olive Male Medulla oblongata Mice Mice, Inbred C57BL Neural Pathways - anatomy & histology Neural Pathways - metabolism Olivary Nucleus - anatomy & histology Olivary Nucleus - metabolism Phenotype Protocadherin Purkinje Cells - physiology Red nucleus RRID:AB_2017112 RRID:AB_2313920 Sensory neurons Spinal cord Zebrin II |
title | Cerebellar modules in the olivo‐cortico‐nuclear loop demarcated by pcdh10 expression in the adult mouse |
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