Application of Fluoro-Jade C in Acute and Chronic Neurodegeneration Models: Utilities and Staining Differences
Recent neuropathological studies have shown that Fluoro-Jade C (FJC), an anionic fluorescent dye, is a good marker of degenerating neurons. However, those studies have mostly examined acute rather than chronic models of neurodegeneration. We therefore compared FJC staining using the intrastriatal 6-...
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Veröffentlicht in: | ACTA HISTOCHEMICA ET CYTOCHEMICA 2009, Vol.42(6), pp.171-179 |
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description | Recent neuropathological studies have shown that Fluoro-Jade C (FJC), an anionic fluorescent dye, is a good marker of degenerating neurons. However, those studies have mostly examined acute rather than chronic models of neurodegeneration. We therefore compared FJC staining using the intrastriatal 6-hydroxydopamine (6-OHDA)-injected rat as an acute model and the zitter rat as a chronic model, as both show dopaminergic (DA) neurodegeneration. In the 6-OHDA-injected rat, FJC-positive neurons were found in the substantia nigra pars compacta (SNc) before the loss of tyrosine hydroxylase (TH)-positive DA neurons. In the zitter rat, FJC-labeled fibers were first detected at 1 month old (1M) and were considerably increased in the striatum at 4M, whereas FJC-labeled cell bodies were found at 4M, but not at 1M in the SNc. Furthermore, FJC-labeled neurons of the zitter rat showed TH-immunoreactivity in fibers, but little in cell bodies, while those from the 6-OHDA-injected rat showed TH-immunoreactivity even in the cell bodies. These results demonstrate that FJC is a useful tool for detecting chronically degenerating neurons, and suggest that intracellular substances bound to FJC may accumulate in the cell bodies from fibers at a slower rate in the chronic model than in the acute model. |
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However, those studies have mostly examined acute rather than chronic models of neurodegeneration. We therefore compared FJC staining using the intrastriatal 6-hydroxydopamine (6-OHDA)-injected rat as an acute model and the zitter rat as a chronic model, as both show dopaminergic (DA) neurodegeneration. In the 6-OHDA-injected rat, FJC-positive neurons were found in the substantia nigra pars compacta (SNc) before the loss of tyrosine hydroxylase (TH)-positive DA neurons. In the zitter rat, FJC-labeled fibers were first detected at 1 month old (1M) and were considerably increased in the striatum at 4M, whereas FJC-labeled cell bodies were found at 4M, but not at 1M in the SNc. Furthermore, FJC-labeled neurons of the zitter rat showed TH-immunoreactivity in fibers, but little in cell bodies, while those from the 6-OHDA-injected rat showed TH-immunoreactivity even in the cell bodies. These results demonstrate that FJC is a useful tool for detecting chronically degenerating neurons, and suggest that intracellular substances bound to FJC may accumulate in the cell bodies from fibers at a slower rate in the chronic model than in the acute model.</description><identifier>ISSN: 0044-5991</identifier><identifier>EISSN: 1347-5800</identifier><identifier>DOI: 10.1267/ahc.09018</identifier><identifier>PMID: 20126570</identifier><language>eng</language><publisher>Japan: JAPAN SOCIETY OF HISTOCHEMISTRY AND CYTOCHEMISTRY</publisher><subject>6-OHDA ; chronic neurodegenerative model ; dopaminergic neurons ; Fluoro-Jade C ; Regular ; zitter rat</subject><ispartof>ACTA HISTOCHEMICA ET CYTOCHEMICA, 2009, Vol.42(6), pp.171-179</ispartof><rights>2009 By the Japan Society of Histochemistry and Cytochemistry</rights><rights>2009 The Japan Society of Histochemistry and Cytochemistry 2009</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c652t-381a54378eeb4df5be689332f611034c4806373099cb6e17fca95c82b6c75fc93</citedby><cites>FETCH-LOGICAL-c652t-381a54378eeb4df5be689332f611034c4806373099cb6e17fca95c82b6c75fc93</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/PMC2808500/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2808500/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,1883,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20126570$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ehara, Ayuka</creatorcontrib><creatorcontrib>Ueda, Shuichi</creatorcontrib><title>Application of Fluoro-Jade C in Acute and Chronic Neurodegeneration Models: Utilities and Staining Differences</title><title>ACTA HISTOCHEMICA ET CYTOCHEMICA</title><addtitle>Acta Histochem. Cytochem.</addtitle><description>Recent neuropathological studies have shown that Fluoro-Jade C (FJC), an anionic fluorescent dye, is a good marker of degenerating neurons. However, those studies have mostly examined acute rather than chronic models of neurodegeneration. We therefore compared FJC staining using the intrastriatal 6-hydroxydopamine (6-OHDA)-injected rat as an acute model and the zitter rat as a chronic model, as both show dopaminergic (DA) neurodegeneration. In the 6-OHDA-injected rat, FJC-positive neurons were found in the substantia nigra pars compacta (SNc) before the loss of tyrosine hydroxylase (TH)-positive DA neurons. In the zitter rat, FJC-labeled fibers were first detected at 1 month old (1M) and were considerably increased in the striatum at 4M, whereas FJC-labeled cell bodies were found at 4M, but not at 1M in the SNc. Furthermore, FJC-labeled neurons of the zitter rat showed TH-immunoreactivity in fibers, but little in cell bodies, while those from the 6-OHDA-injected rat showed TH-immunoreactivity even in the cell bodies. These results demonstrate that FJC is a useful tool for detecting chronically degenerating neurons, and suggest that intracellular substances bound to FJC may accumulate in the cell bodies from fibers at a slower rate in the chronic model than in the acute model.</description><subject>6-OHDA</subject><subject>chronic neurodegenerative model</subject><subject>dopaminergic neurons</subject><subject>Fluoro-Jade C</subject><subject>Regular</subject><subject>zitter rat</subject><issn>0044-5991</issn><issn>1347-5800</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNp9kU2PFCEQhonRuOPqwT9gOGk89AoNdIOHNZPR9SOrHnTPhKaLGTY9MAJt4r-XmVknevECoeqpJxVehJ5SckHbrn9lNvaCKELlPbSgjPeNkITcRwtCOG-EUvQMPcr5llSilh6is5bUOdGTBQrL3W7y1hQfA44OX01zTLH5ZEbAK-wDXtq5ADZhxKtNisFb_AXmFEdYQ4B0nPtcn1N-jW-Kn3zxkA_8t2J88GGN33rnIEGwkB-jB85MGZ7c3efo5urd99WH5vrr-4-r5XVjO9GWhklqBGe9BBj46MQAnVSMta6jlDBuuSQd6xlRyg4d0N5Zo4SV7dDZXjir2Dm6PHp387CF0UIoyUx6l_zWpF86Gq__7QS_0ev4U7eSSEFIFby4E6T4Y4Zc9NZnC9NkAsQ5654xwalUtJLP_0u29atJ3-3Bl0fQpphzAndahxK9z1HXHPUhx8o--3v_E_knuAq8OQK3uZg1nACTircTHFS81d3-OChPHbsxSUNgvwHxnLAm</recordid><startdate>20090101</startdate><enddate>20090101</enddate><creator>Ehara, Ayuka</creator><creator>Ueda, Shuichi</creator><general>JAPAN SOCIETY OF HISTOCHEMISTRY AND CYTOCHEMISTRY</general><general>Japan Society of Histochemistry and Cytochemistry</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20090101</creationdate><title>Application of Fluoro-Jade C in Acute and Chronic Neurodegeneration Models: Utilities and Staining Differences</title><author>Ehara, Ayuka ; Ueda, Shuichi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c652t-381a54378eeb4df5be689332f611034c4806373099cb6e17fca95c82b6c75fc93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>6-OHDA</topic><topic>chronic neurodegenerative model</topic><topic>dopaminergic neurons</topic><topic>Fluoro-Jade C</topic><topic>Regular</topic><topic>zitter rat</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ehara, Ayuka</creatorcontrib><creatorcontrib>Ueda, Shuichi</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>ACTA HISTOCHEMICA ET CYTOCHEMICA</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ehara, Ayuka</au><au>Ueda, Shuichi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Application of Fluoro-Jade C in Acute and Chronic Neurodegeneration Models: Utilities and Staining Differences</atitle><jtitle>ACTA HISTOCHEMICA ET CYTOCHEMICA</jtitle><addtitle>Acta Histochem. Cytochem.</addtitle><date>2009-01-01</date><risdate>2009</risdate><volume>42</volume><issue>6</issue><spage>171</spage><epage>179</epage><pages>171-179</pages><issn>0044-5991</issn><eissn>1347-5800</eissn><abstract>Recent neuropathological studies have shown that Fluoro-Jade C (FJC), an anionic fluorescent dye, is a good marker of degenerating neurons. However, those studies have mostly examined acute rather than chronic models of neurodegeneration. We therefore compared FJC staining using the intrastriatal 6-hydroxydopamine (6-OHDA)-injected rat as an acute model and the zitter rat as a chronic model, as both show dopaminergic (DA) neurodegeneration. In the 6-OHDA-injected rat, FJC-positive neurons were found in the substantia nigra pars compacta (SNc) before the loss of tyrosine hydroxylase (TH)-positive DA neurons. In the zitter rat, FJC-labeled fibers were first detected at 1 month old (1M) and were considerably increased in the striatum at 4M, whereas FJC-labeled cell bodies were found at 4M, but not at 1M in the SNc. Furthermore, FJC-labeled neurons of the zitter rat showed TH-immunoreactivity in fibers, but little in cell bodies, while those from the 6-OHDA-injected rat showed TH-immunoreactivity even in the cell bodies. These results demonstrate that FJC is a useful tool for detecting chronically degenerating neurons, and suggest that intracellular substances bound to FJC may accumulate in the cell bodies from fibers at a slower rate in the chronic model than in the acute model.</abstract><cop>Japan</cop><pub>JAPAN SOCIETY OF HISTOCHEMISTRY AND CYTOCHEMISTRY</pub><pmid>20126570</pmid><doi>10.1267/ahc.09018</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 6-OHDA chronic neurodegenerative model dopaminergic neurons Fluoro-Jade C Regular zitter rat |
title | Application of Fluoro-Jade C in Acute and Chronic Neurodegeneration Models: Utilities and Staining Differences |
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