Abnormal expression of tyrosine hydroxylase immunoreactivity in cerebellar cortex of ataxic mutant mice
Expression of tyrosine hydroxylase (TH) was examined immunohistochemically in the cerebellum of two ataxic mutants, Rolling mouse Nagoya (RMN) and dilute-lethal mice (DL). In littermate controls of both mutants, a few TH-positive Purkinje cells were distributed sparsely and their number was smaller...
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Veröffentlicht in: | Brain research 1999-05, Vol.829 (1), p.107-112 |
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creator | Sawada, Kazuhiko Komatsu, Suguru Haga, Hiromi Sun, Xue-Zhi Hisano, Setsuji Fukui, Yoshihiro |
description | Expression of tyrosine hydroxylase (TH) was examined immunohistochemically in the cerebellum of two ataxic mutants, Rolling mouse Nagoya (RMN) and
dilute-lethal mice (DL). In littermate controls of both mutants, a few TH-positive Purkinje cells were distributed sparsely and their number was smaller than in the mutants at any ages examined. In RMN, TH-positive Purkinje cells were distributed in lobule IX and X, and were arranged into parasagittal bands at 2 weeks of age. TH-positive Purkinje cells increased in number and were widely distributed throughout the vermis at 3 weeks of age. In adult RMN, TH-positive Purkinje cells were found in all lobules of the cerebellum. Their parasagittal bands also became evident in the hemisphere. In DL, TH-positive Purkinje cells were mainly distributed in vermal lobules IX and X, and the flocculus at 3 weeks of age. They were also found as bands in lobules IX and X. The results suggest that abnormal expression of TH in Purkinje cells may not be specific to the allelic group. Since TH promoter is activated by Ca
2+, TH expression in the mutant Purkinje cells may predict neuronal dysfunction caused by alterations in cellular Ca
2+ currents. |
doi_str_mv | 10.1016/S0006-8993(99)01347-5 |
format | Article |
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dilute-lethal mice (DL). In littermate controls of both mutants, a few TH-positive Purkinje cells were distributed sparsely and their number was smaller than in the mutants at any ages examined. In RMN, TH-positive Purkinje cells were distributed in lobule IX and X, and were arranged into parasagittal bands at 2 weeks of age. TH-positive Purkinje cells increased in number and were widely distributed throughout the vermis at 3 weeks of age. In adult RMN, TH-positive Purkinje cells were found in all lobules of the cerebellum. Their parasagittal bands also became evident in the hemisphere. In DL, TH-positive Purkinje cells were mainly distributed in vermal lobules IX and X, and the flocculus at 3 weeks of age. They were also found as bands in lobules IX and X. The results suggest that abnormal expression of TH in Purkinje cells may not be specific to the allelic group. Since TH promoter is activated by Ca
2+, TH expression in the mutant Purkinje cells may predict neuronal dysfunction caused by alterations in cellular Ca
2+ currents.</description><identifier>ISSN: 0006-8993</identifier><identifier>EISSN: 1872-6240</identifier><identifier>DOI: 10.1016/S0006-8993(99)01347-5</identifier><identifier>PMID: 10350535</identifier><identifier>CODEN: BRREAP</identifier><language>eng</language><publisher>London: Elsevier B.V</publisher><subject>Animals ; Biological and medical sciences ; Calcium Channels - physiology ; Cerebellar Ataxia - enzymology ; Cerebellum ; Hereditary ataxia ; Immunohistochemistry ; Medical sciences ; Mice ; Mice, Neurologic Mutants ; Nervous system involvement in other diseases. Miscellaneous ; Neurology ; Neurons - enzymology ; Purkinje cell ; Tyrosine 3-Monooxygenase - analysis ; Tyrosine hydroxylase</subject><ispartof>Brain research, 1999-05, Vol.829 (1), p.107-112</ispartof><rights>1999 Elsevier Science B.V.</rights><rights>1999 INIST-CNRS</rights><rights>Copyright 1999 Elsevier Science B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c539t-ff08c4e2dba396418f3e48354ccc2e07f643e98362eba52941c1111292f7cad53</citedby><cites>FETCH-LOGICAL-c539t-ff08c4e2dba396418f3e48354ccc2e07f643e98362eba52941c1111292f7cad53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0006-8993(99)01347-5$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27926,27927,45997</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1832251$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10350535$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sawada, Kazuhiko</creatorcontrib><creatorcontrib>Komatsu, Suguru</creatorcontrib><creatorcontrib>Haga, Hiromi</creatorcontrib><creatorcontrib>Sun, Xue-Zhi</creatorcontrib><creatorcontrib>Hisano, Setsuji</creatorcontrib><creatorcontrib>Fukui, Yoshihiro</creatorcontrib><title>Abnormal expression of tyrosine hydroxylase immunoreactivity in cerebellar cortex of ataxic mutant mice</title><title>Brain research</title><addtitle>Brain Res</addtitle><description>Expression of tyrosine hydroxylase (TH) was examined immunohistochemically in the cerebellum of two ataxic mutants, Rolling mouse Nagoya (RMN) and
dilute-lethal mice (DL). In littermate controls of both mutants, a few TH-positive Purkinje cells were distributed sparsely and their number was smaller than in the mutants at any ages examined. In RMN, TH-positive Purkinje cells were distributed in lobule IX and X, and were arranged into parasagittal bands at 2 weeks of age. TH-positive Purkinje cells increased in number and were widely distributed throughout the vermis at 3 weeks of age. In adult RMN, TH-positive Purkinje cells were found in all lobules of the cerebellum. Their parasagittal bands also became evident in the hemisphere. In DL, TH-positive Purkinje cells were mainly distributed in vermal lobules IX and X, and the flocculus at 3 weeks of age. They were also found as bands in lobules IX and X. The results suggest that abnormal expression of TH in Purkinje cells may not be specific to the allelic group. Since TH promoter is activated by Ca
2+, TH expression in the mutant Purkinje cells may predict neuronal dysfunction caused by alterations in cellular Ca
2+ currents.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Calcium Channels - physiology</subject><subject>Cerebellar Ataxia - enzymology</subject><subject>Cerebellum</subject><subject>Hereditary ataxia</subject><subject>Immunohistochemistry</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Neurologic Mutants</subject><subject>Nervous system involvement in other diseases. Miscellaneous</subject><subject>Neurology</subject><subject>Neurons - enzymology</subject><subject>Purkinje cell</subject><subject>Tyrosine 3-Monooxygenase - analysis</subject><subject>Tyrosine hydroxylase</subject><issn>0006-8993</issn><issn>1872-6240</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU9v1DAQxS0EotvCRwD5gBAcAv4TJ5lTVVUUkCpxAM6WM5mAURIvtlNtvj1JdwXcOpfRSL-ZeXqPsRdSvJNCVu-_CiGqogHQbwDeCqnLujCP2E42tSoqVYrHbPcXOWPnKf1aR61BPGVnUmgjjDY79uOqnUIc3cDpsI-Ukg8TDz3PSwzJT8R_Ll0Mh2Vwibgfx3mlyWH2dz4v3E8cKVJLw-AixxAzHbZtl93BIx_n7KbMR4_0jD3p3ZDo-alfsO83H75dfypuv3z8fH11W6DRkIu-Fw2WpLrWaahK2fSaykabEhEVibqvSk3Q6EpR64yCUqJcS4Hqa3Sd0Rfs9fHuPobfM6VsR59w0zdRmJOtoAYDIB8EZa0aDVCvoDmCuDqSIvV2H_3o4mKlsFsU9j4Ku_lsAex9FHZT8vL0YG5H6v7bOnq_Aq9OgEvohj66CX36xzVaKbMJvTxitNp25ynahJ4mpM5Hwmy74B9Q8gcvWac4</recordid><startdate>19990522</startdate><enddate>19990522</enddate><creator>Sawada, Kazuhiko</creator><creator>Komatsu, Suguru</creator><creator>Haga, Hiromi</creator><creator>Sun, Xue-Zhi</creator><creator>Hisano, Setsuji</creator><creator>Fukui, Yoshihiro</creator><general>Elsevier B.V</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>19990522</creationdate><title>Abnormal expression of tyrosine hydroxylase immunoreactivity in cerebellar cortex of ataxic mutant mice</title><author>Sawada, Kazuhiko ; Komatsu, Suguru ; Haga, Hiromi ; Sun, Xue-Zhi ; Hisano, Setsuji ; Fukui, Yoshihiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c539t-ff08c4e2dba396418f3e48354ccc2e07f643e98362eba52941c1111292f7cad53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Calcium Channels - physiology</topic><topic>Cerebellar Ataxia - enzymology</topic><topic>Cerebellum</topic><topic>Hereditary ataxia</topic><topic>Immunohistochemistry</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Neurologic Mutants</topic><topic>Nervous system involvement in other diseases. Miscellaneous</topic><topic>Neurology</topic><topic>Neurons - enzymology</topic><topic>Purkinje cell</topic><topic>Tyrosine 3-Monooxygenase - analysis</topic><topic>Tyrosine hydroxylase</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sawada, Kazuhiko</creatorcontrib><creatorcontrib>Komatsu, Suguru</creatorcontrib><creatorcontrib>Haga, Hiromi</creatorcontrib><creatorcontrib>Sun, Xue-Zhi</creatorcontrib><creatorcontrib>Hisano, Setsuji</creatorcontrib><creatorcontrib>Fukui, Yoshihiro</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>Brain research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sawada, Kazuhiko</au><au>Komatsu, Suguru</au><au>Haga, Hiromi</au><au>Sun, Xue-Zhi</au><au>Hisano, Setsuji</au><au>Fukui, Yoshihiro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Abnormal expression of tyrosine hydroxylase immunoreactivity in cerebellar cortex of ataxic mutant mice</atitle><jtitle>Brain research</jtitle><addtitle>Brain Res</addtitle><date>1999-05-22</date><risdate>1999</risdate><volume>829</volume><issue>1</issue><spage>107</spage><epage>112</epage><pages>107-112</pages><issn>0006-8993</issn><eissn>1872-6240</eissn><coden>BRREAP</coden><abstract>Expression of tyrosine hydroxylase (TH) was examined immunohistochemically in the cerebellum of two ataxic mutants, Rolling mouse Nagoya (RMN) and
dilute-lethal mice (DL). In littermate controls of both mutants, a few TH-positive Purkinje cells were distributed sparsely and their number was smaller than in the mutants at any ages examined. In RMN, TH-positive Purkinje cells were distributed in lobule IX and X, and were arranged into parasagittal bands at 2 weeks of age. TH-positive Purkinje cells increased in number and were widely distributed throughout the vermis at 3 weeks of age. In adult RMN, TH-positive Purkinje cells were found in all lobules of the cerebellum. Their parasagittal bands also became evident in the hemisphere. In DL, TH-positive Purkinje cells were mainly distributed in vermal lobules IX and X, and the flocculus at 3 weeks of age. They were also found as bands in lobules IX and X. The results suggest that abnormal expression of TH in Purkinje cells may not be specific to the allelic group. Since TH promoter is activated by Ca
2+, TH expression in the mutant Purkinje cells may predict neuronal dysfunction caused by alterations in cellular Ca
2+ currents.</abstract><cop>London</cop><cop>Amsterdam</cop><cop>New York, NY</cop><pub>Elsevier B.V</pub><pmid>10350535</pmid><doi>10.1016/S0006-8993(99)01347-5</doi><tpages>6</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Calcium Channels - physiology Cerebellar Ataxia - enzymology Cerebellum Hereditary ataxia Immunohistochemistry Medical sciences Mice Mice, Neurologic Mutants Nervous system involvement in other diseases. Miscellaneous Neurology Neurons - enzymology Purkinje cell Tyrosine 3-Monooxygenase - analysis Tyrosine hydroxylase |
title | Abnormal expression of tyrosine hydroxylase immunoreactivity in cerebellar cortex of ataxic mutant mice |
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