Kainate-induced endocytosis in retinal amacrine cells
Endocytosis is enhanced in some cases of neuronal death. We report for the first time that intraocular injections, in chick embryos, of excitotoxic doses of kainate induce strong endocytosis in retinal amacrine cells destined to die and that even subtoxic doses can induce some degree of endocytosis....
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Veröffentlicht in: | Journal of comparative neurology (1911) 2003-10, Vol.465 (2), p.286-295 |
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container_title | Journal of comparative neurology (1911) |
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creator | Borsello, Tiziana Bressoud, Raymond Mottier, Vincent González, Nicolas Gomez, Gabriel Clarke, Peter G.H. |
description | Endocytosis is enhanced in some cases of neuronal death. We report for the first time that intraocular injections, in chick embryos, of excitotoxic doses of kainate induce strong endocytosis in retinal amacrine cells destined to die and that even subtoxic doses can induce some degree of endocytosis. That the uptake was due to endocytosis rather than passive diffusion through the plasma membrane was shown ultrastructurally. The endocytosis was demonstrated by using three unrelated tracers—horseradish peroxidase, microperoxidase, and 4.4‐kDa fluorescein isothiocyanate (FITC)‐labeled dextran—suggesting that it does not depend on the binding of the tracers to a particular receptor. However, it appears to be surprisingly sensitive to the size of the ligand, because a heavier (42‐kDa) FITC‐dextran was not endocytosed. The induction of endocytosis by kainate can occur even when protein synthesis is blocked. These results indicate that toxic or near‐toxic doses of kainate induce endocytosis, raising the question of whether this is mechanistically implicated in causing or preventing excitotoxic neuronal death. J. Comp. Neurol. 465:286–295, 2003. © 2003 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/cne.10834 |
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We report for the first time that intraocular injections, in chick embryos, of excitotoxic doses of kainate induce strong endocytosis in retinal amacrine cells destined to die and that even subtoxic doses can induce some degree of endocytosis. That the uptake was due to endocytosis rather than passive diffusion through the plasma membrane was shown ultrastructurally. The endocytosis was demonstrated by using three unrelated tracers—horseradish peroxidase, microperoxidase, and 4.4‐kDa fluorescein isothiocyanate (FITC)‐labeled dextran—suggesting that it does not depend on the binding of the tracers to a particular receptor. However, it appears to be surprisingly sensitive to the size of the ligand, because a heavier (42‐kDa) FITC‐dextran was not endocytosed. The induction of endocytosis by kainate can occur even when protein synthesis is blocked. These results indicate that toxic or near‐toxic doses of kainate induce endocytosis, raising the question of whether this is mechanistically implicated in causing or preventing excitotoxic neuronal death. J. Comp. Neurol. 465:286–295, 2003. © 2003 Wiley‐Liss, Inc.</description><identifier>ISSN: 0021-9967</identifier><identifier>EISSN: 1096-9861</identifier><identifier>DOI: 10.1002/cne.10834</identifier><identifier>PMID: 12949787</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Amacrine Cells - drug effects ; Amacrine Cells - metabolism ; Amacrine Cells - pathology ; Amacrine Cells - ultrastructure ; Animals ; Cell Count ; cell death ; Chick Embryo ; Cycloheximide - pharmacology ; DNA Fragmentation - drug effects ; Dose-Response Relationship, Drug ; Endocytosis - drug effects ; Excitatory Amino Acid Agonists - pharmacology ; excitotoxicity ; Fluorescent Antibody Technique ; In Situ Nick-End Labeling ; Kainic Acid - pharmacology ; Microscopy, Electron ; nervous system ; Protein Synthesis Inhibitors - pharmacology ; retina ; ultrastructure</subject><ispartof>Journal of comparative neurology (1911), 2003-10, Vol.465 (2), p.286-295</ispartof><rights>Copyright © 2003 Wiley‐Liss, Inc.</rights><rights>Copyright 2003 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3904-f36c153ad87301f36837b33781b5882026fa7762fd842f577e024e44239581763</citedby><cites>FETCH-LOGICAL-c3904-f36c153ad87301f36837b33781b5882026fa7762fd842f577e024e44239581763</cites></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.10834$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fcne.10834$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12949787$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Borsello, Tiziana</creatorcontrib><creatorcontrib>Bressoud, Raymond</creatorcontrib><creatorcontrib>Mottier, Vincent</creatorcontrib><creatorcontrib>González, Nicolas</creatorcontrib><creatorcontrib>Gomez, Gabriel</creatorcontrib><creatorcontrib>Clarke, Peter G.H.</creatorcontrib><title>Kainate-induced endocytosis in retinal amacrine cells</title><title>Journal of comparative neurology (1911)</title><addtitle>J. Comp. Neurol</addtitle><description>Endocytosis is enhanced in some cases of neuronal death. We report for the first time that intraocular injections, in chick embryos, of excitotoxic doses of kainate induce strong endocytosis in retinal amacrine cells destined to die and that even subtoxic doses can induce some degree of endocytosis. That the uptake was due to endocytosis rather than passive diffusion through the plasma membrane was shown ultrastructurally. The endocytosis was demonstrated by using three unrelated tracers—horseradish peroxidase, microperoxidase, and 4.4‐kDa fluorescein isothiocyanate (FITC)‐labeled dextran—suggesting that it does not depend on the binding of the tracers to a particular receptor. However, it appears to be surprisingly sensitive to the size of the ligand, because a heavier (42‐kDa) FITC‐dextran was not endocytosed. The induction of endocytosis by kainate can occur even when protein synthesis is blocked. These results indicate that toxic or near‐toxic doses of kainate induce endocytosis, raising the question of whether this is mechanistically implicated in causing or preventing excitotoxic neuronal death. J. Comp. Neurol. 465:286–295, 2003. © 2003 Wiley‐Liss, Inc.</description><subject>Amacrine Cells - drug effects</subject><subject>Amacrine Cells - metabolism</subject><subject>Amacrine Cells - pathology</subject><subject>Amacrine Cells - ultrastructure</subject><subject>Animals</subject><subject>Cell Count</subject><subject>cell death</subject><subject>Chick Embryo</subject><subject>Cycloheximide - pharmacology</subject><subject>DNA Fragmentation - drug effects</subject><subject>Dose-Response Relationship, Drug</subject><subject>Endocytosis - drug effects</subject><subject>Excitatory Amino Acid Agonists - pharmacology</subject><subject>excitotoxicity</subject><subject>Fluorescent Antibody Technique</subject><subject>In Situ Nick-End Labeling</subject><subject>Kainic Acid - pharmacology</subject><subject>Microscopy, Electron</subject><subject>nervous system</subject><subject>Protein Synthesis Inhibitors - pharmacology</subject><subject>retina</subject><subject>ultrastructure</subject><issn>0021-9967</issn><issn>1096-9861</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kEtPwzAQhC0EoqVw4A-gnJA4hPoVP44QlfKoCgcQEhfLdRzJkCbFTgT997ikwInT7mq-Ga0GgGMEzxGEeGxqGxdB6A4YIihZKgVDu2AYNZRKyfgAHITwCiGUkoh9MEBYUskFH4LsTrtatzZ1ddEZWyS2LhqzbpvgQuLqxNs26lWil9p4V9vE2KoKh2Cv1FWwR9s5Ak9Xk8f8Op3dT2_yi1lqiIQ0LQkzKCO6EJxAFC9B-IIQLtAiEwJDzErNOcNlISguM84txNRSionMBOKMjMBpn7vyzXtnQ6uWLmw-0LVtuqCQkBRmkEfwrAeNb0LwtlQr75barxWCatORih2p744ie7IN7RZLW_yR21IiMO6BD1fZ9f9JKp9PfiLT3uFCaz9_Hdq_KcYJz9TzfKou81tJH-iLmpMvzqF80A</recordid><startdate>20031013</startdate><enddate>20031013</enddate><creator>Borsello, Tiziana</creator><creator>Bressoud, Raymond</creator><creator>Mottier, Vincent</creator><creator>González, Nicolas</creator><creator>Gomez, Gabriel</creator><creator>Clarke, Peter G.H.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</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>7TK</scope></search><sort><creationdate>20031013</creationdate><title>Kainate-induced endocytosis in retinal amacrine cells</title><author>Borsello, Tiziana ; Bressoud, Raymond ; Mottier, Vincent ; González, Nicolas ; Gomez, Gabriel ; Clarke, Peter G.H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3904-f36c153ad87301f36837b33781b5882026fa7762fd842f577e024e44239581763</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Amacrine Cells - drug effects</topic><topic>Amacrine Cells - metabolism</topic><topic>Amacrine Cells - pathology</topic><topic>Amacrine Cells - ultrastructure</topic><topic>Animals</topic><topic>Cell Count</topic><topic>cell death</topic><topic>Chick Embryo</topic><topic>Cycloheximide - pharmacology</topic><topic>DNA Fragmentation - drug effects</topic><topic>Dose-Response Relationship, Drug</topic><topic>Endocytosis - drug effects</topic><topic>Excitatory Amino Acid Agonists - pharmacology</topic><topic>excitotoxicity</topic><topic>Fluorescent Antibody Technique</topic><topic>In Situ Nick-End Labeling</topic><topic>Kainic Acid - pharmacology</topic><topic>Microscopy, Electron</topic><topic>nervous system</topic><topic>Protein Synthesis Inhibitors - pharmacology</topic><topic>retina</topic><topic>ultrastructure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Borsello, Tiziana</creatorcontrib><creatorcontrib>Bressoud, Raymond</creatorcontrib><creatorcontrib>Mottier, Vincent</creatorcontrib><creatorcontrib>González, Nicolas</creatorcontrib><creatorcontrib>Gomez, Gabriel</creatorcontrib><creatorcontrib>Clarke, Peter G.H.</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>Neurosciences Abstracts</collection><jtitle>Journal of comparative neurology (1911)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Borsello, Tiziana</au><au>Bressoud, Raymond</au><au>Mottier, Vincent</au><au>González, Nicolas</au><au>Gomez, Gabriel</au><au>Clarke, Peter G.H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Kainate-induced endocytosis in retinal amacrine cells</atitle><jtitle>Journal of comparative neurology (1911)</jtitle><addtitle>J. Comp. Neurol</addtitle><date>2003-10-13</date><risdate>2003</risdate><volume>465</volume><issue>2</issue><spage>286</spage><epage>295</epage><pages>286-295</pages><issn>0021-9967</issn><eissn>1096-9861</eissn><abstract>Endocytosis is enhanced in some cases of neuronal death. We report for the first time that intraocular injections, in chick embryos, of excitotoxic doses of kainate induce strong endocytosis in retinal amacrine cells destined to die and that even subtoxic doses can induce some degree of endocytosis. That the uptake was due to endocytosis rather than passive diffusion through the plasma membrane was shown ultrastructurally. The endocytosis was demonstrated by using three unrelated tracers—horseradish peroxidase, microperoxidase, and 4.4‐kDa fluorescein isothiocyanate (FITC)‐labeled dextran—suggesting that it does not depend on the binding of the tracers to a particular receptor. However, it appears to be surprisingly sensitive to the size of the ligand, because a heavier (42‐kDa) FITC‐dextran was not endocytosed. The induction of endocytosis by kainate can occur even when protein synthesis is blocked. These results indicate that toxic or near‐toxic doses of kainate induce endocytosis, raising the question of whether this is mechanistically implicated in causing or preventing excitotoxic neuronal death. J. Comp. Neurol. 465:286–295, 2003. © 2003 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>12949787</pmid><doi>10.1002/cne.10834</doi><tpages>10</tpages></addata></record> |
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subjects | Amacrine Cells - drug effects Amacrine Cells - metabolism Amacrine Cells - pathology Amacrine Cells - ultrastructure Animals Cell Count cell death Chick Embryo Cycloheximide - pharmacology DNA Fragmentation - drug effects Dose-Response Relationship, Drug Endocytosis - drug effects Excitatory Amino Acid Agonists - pharmacology excitotoxicity Fluorescent Antibody Technique In Situ Nick-End Labeling Kainic Acid - pharmacology Microscopy, Electron nervous system Protein Synthesis Inhibitors - pharmacology retina ultrastructure |
title | Kainate-induced endocytosis in retinal amacrine cells |
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