Calcium currents in rat cerebellar purkinje cells maintained in culture
Calcium permeabilities were examined in large cerebellar neurons maintained in culture, and morphologically identified as Purkinje cells. When cells were supplied with a Dulbecco Minimum Eagle's Medium with 10% horse serum added (5–10 days), somatic recordings revealed complex spikes and these...
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Veröffentlicht in: | Neuroscience 1989, Vol.30 (3), p.605-617 |
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description | Calcium permeabilities were examined in large cerebellar neurons maintained in culture, and morphologically identified as Purkinje cells. When cells were supplied with a Dulbecco Minimum Eagle's Medium with 10% horse serum added (5–10 days), somatic recordings revealed complex spikes and these were shown to be generated by Na and Ca components, the Na one being tetrodotoxin-sensitive. At the dendritic level, Ca currents were better resolved than at the soma. In dendrites, Ca entry was shown to occur through at least two distinct currents. The first was a low-threshold transient current (elicited above −60 mV from a holding potential of −80 mV) which was reduced by almost 30% by 50μ M cadmium. The second was a high-threshold current (above −20 mV) which gave rise to (1) a transient component exhibiting a steady-state inactivation and so requiring holding potentials at −80 mV, and (2) a sustained component. Both components were suppressed by 50 μm cadmium. We measured a total Ca current at the dendritic level reaching values of up to 1 nA.
In another culture medium (Leibovitz medium) known to allow expression of three types of calcium currents in nodose cells we observed the development of the dendritic tree of Purkinje cells but with no simultaneous expression of the high-threshold Ca current. |
doi_str_mv | 10.1016/0306-4522(89)90155-3 |
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In another culture medium (Leibovitz medium) known to allow expression of three types of calcium currents in nodose cells we observed the development of the dendritic tree of Purkinje cells but with no simultaneous expression of the high-threshold Ca current.</description><identifier>ISSN: 0306-4522</identifier><identifier>EISSN: 1873-7544</identifier><identifier>DOI: 10.1016/0306-4522(89)90155-3</identifier><identifier>PMID: 2771040</identifier><identifier>CODEN: NRSCDN</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Action Potentials - drug effects ; Animals ; Animals, Newborn ; Biological and medical sciences ; Cadmium - pharmacology ; Calcium - physiology ; Cells, Cultured ; Central nervous system ; Dendrites - physiology ; Electrophysiology ; Fundamental and applied biological sciences. Psychology ; Purkinje Cells - cytology ; Purkinje Cells - drug effects ; Purkinje Cells - physiology ; Rats ; Tetrodotoxin - pharmacology ; Vertebrates: nervous system and sense organs</subject><ispartof>Neuroscience, 1989, Vol.30 (3), p.605-617</ispartof><rights>1989 IBRO</rights><rights>1990 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c512t-5099fe2e20da7588d3066654f6eb3c298b0eca02c9087f614af951870d149a13</citedby><cites>FETCH-LOGICAL-c512t-5099fe2e20da7588d3066654f6eb3c298b0eca02c9087f614af951870d149a13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/0306452289901553$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,4009,27902,27903,27904,65309</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=6829011$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2771040$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bossu, J.-L.</creatorcontrib><creatorcontrib>Dupont, J.-L.</creatorcontrib><creatorcontrib>Feltz, A.</creatorcontrib><title>Calcium currents in rat cerebellar purkinje cells maintained in culture</title><title>Neuroscience</title><addtitle>Neuroscience</addtitle><description>Calcium permeabilities were examined in large cerebellar neurons maintained in culture, and morphologically identified as Purkinje cells. When cells were supplied with a Dulbecco Minimum Eagle's Medium with 10% horse serum added (5–10 days), somatic recordings revealed complex spikes and these were shown to be generated by Na and Ca components, the Na one being tetrodotoxin-sensitive. At the dendritic level, Ca currents were better resolved than at the soma. In dendrites, Ca entry was shown to occur through at least two distinct currents. The first was a low-threshold transient current (elicited above −60 mV from a holding potential of −80 mV) which was reduced by almost 30% by 50μ M cadmium. The second was a high-threshold current (above −20 mV) which gave rise to (1) a transient component exhibiting a steady-state inactivation and so requiring holding potentials at −80 mV, and (2) a sustained component. Both components were suppressed by 50 μm cadmium. We measured a total Ca current at the dendritic level reaching values of up to 1 nA.
In another culture medium (Leibovitz medium) known to allow expression of three types of calcium currents in nodose cells we observed the development of the dendritic tree of Purkinje cells but with no simultaneous expression of the high-threshold Ca current.</description><subject>Action Potentials - drug effects</subject><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Biological and medical sciences</subject><subject>Cadmium - pharmacology</subject><subject>Calcium - physiology</subject><subject>Cells, Cultured</subject><subject>Central nervous system</subject><subject>Dendrites - physiology</subject><subject>Electrophysiology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Purkinje Cells - cytology</subject><subject>Purkinje Cells - drug effects</subject><subject>Purkinje Cells - physiology</subject><subject>Rats</subject><subject>Tetrodotoxin - pharmacology</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0306-4522</issn><issn>1873-7544</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1LxDAQhoMo67r6DxR6ENFDNZ9tchFk0VVY8LL3kKZTiKbtmrSC_97UXfZoIARmnhnePAhdEnxPMCkeMMNFzgWlt1LdKUyEyNkRmhNZsrwUnB-j-QE5RWcxfuB0BGczNKNlSTDHc7RaGm_d2GZ2DAG6IWauy4IZMgsBKvDehGw7hk_XfUCqeR-z1rhuSBfqibWjH8YA5-ikMT7Cxf5doM3L82b5mq_fV2_Lp3VuBaFDLrBSDVCguDalkLJOAYtC8KaAilmqZIXBGkytwrJsCsJNo0T6Ea4JV4awBbrZrd2G_muEOOjWxSmW6aAfoyaCEUK5SiDfgTb0MQZo9Da41oQfTbCe9OnJjZ7caKn0nz7N0tjVfv9YtVAfhva-Uv963zfRGt8E01kXD1ghado0xXzcYZBUfDsIOloHnYXaBbCDrnv3f45fO66KZQ</recordid><startdate>1989</startdate><enddate>1989</enddate><creator>Bossu, J.-L.</creator><creator>Dupont, J.-L.</creator><creator>Feltz, A.</creator><general>Elsevier Ltd</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>7QP</scope><scope>7TK</scope></search><sort><creationdate>1989</creationdate><title>Calcium currents in rat cerebellar purkinje cells maintained in culture</title><author>Bossu, J.-L. ; Dupont, J.-L. ; Feltz, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c512t-5099fe2e20da7588d3066654f6eb3c298b0eca02c9087f614af951870d149a13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Action Potentials - drug effects</topic><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Biological and medical sciences</topic><topic>Cadmium - pharmacology</topic><topic>Calcium - physiology</topic><topic>Cells, Cultured</topic><topic>Central nervous system</topic><topic>Dendrites - physiology</topic><topic>Electrophysiology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Purkinje Cells - cytology</topic><topic>Purkinje Cells - drug effects</topic><topic>Purkinje Cells - physiology</topic><topic>Rats</topic><topic>Tetrodotoxin - pharmacology</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bossu, J.-L.</creatorcontrib><creatorcontrib>Dupont, J.-L.</creatorcontrib><creatorcontrib>Feltz, A.</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>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><jtitle>Neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bossu, J.-L.</au><au>Dupont, J.-L.</au><au>Feltz, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Calcium currents in rat cerebellar purkinje cells maintained in culture</atitle><jtitle>Neuroscience</jtitle><addtitle>Neuroscience</addtitle><date>1989</date><risdate>1989</risdate><volume>30</volume><issue>3</issue><spage>605</spage><epage>617</epage><pages>605-617</pages><issn>0306-4522</issn><eissn>1873-7544</eissn><coden>NRSCDN</coden><abstract>Calcium permeabilities were examined in large cerebellar neurons maintained in culture, and morphologically identified as Purkinje cells. When cells were supplied with a Dulbecco Minimum Eagle's Medium with 10% horse serum added (5–10 days), somatic recordings revealed complex spikes and these were shown to be generated by Na and Ca components, the Na one being tetrodotoxin-sensitive. At the dendritic level, Ca currents were better resolved than at the soma. In dendrites, Ca entry was shown to occur through at least two distinct currents. The first was a low-threshold transient current (elicited above −60 mV from a holding potential of −80 mV) which was reduced by almost 30% by 50μ M cadmium. The second was a high-threshold current (above −20 mV) which gave rise to (1) a transient component exhibiting a steady-state inactivation and so requiring holding potentials at −80 mV, and (2) a sustained component. Both components were suppressed by 50 μm cadmium. We measured a total Ca current at the dendritic level reaching values of up to 1 nA.
In another culture medium (Leibovitz medium) known to allow expression of three types of calcium currents in nodose cells we observed the development of the dendritic tree of Purkinje cells but with no simultaneous expression of the high-threshold Ca current.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>2771040</pmid><doi>10.1016/0306-4522(89)90155-3</doi><tpages>13</tpages></addata></record> |
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subjects | Action Potentials - drug effects Animals Animals, Newborn Biological and medical sciences Cadmium - pharmacology Calcium - physiology Cells, Cultured Central nervous system Dendrites - physiology Electrophysiology Fundamental and applied biological sciences. Psychology Purkinje Cells - cytology Purkinje Cells - drug effects Purkinje Cells - physiology Rats Tetrodotoxin - pharmacology Vertebrates: nervous system and sense organs |
title | Calcium currents in rat cerebellar purkinje cells maintained in culture |
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