Serum from Sydenham's chorea patients modifies intracellular calcium levels in PC12 cells by a complement-independent mechanism.
Identifieur interne : 003120 ( PubMed/Corpus ); précédent : 003119; suivant : 003121Serum from Sydenham's chorea patients modifies intracellular calcium levels in PC12 cells by a complement-independent mechanism.
Auteurs : Antonio L. Teixeira ; Melissa M. Guimarães ; Marco Aurélio Romano-Silva ; Francisco CardosoSource :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 2005.
English descriptors
- KwdEn :
- Adolescent, Animals, Antibodies (pharmacology), Basal Ganglia (immunology), Calcium (metabolism), Child, Chorea (blood), Chorea (immunology), Complement System Proteins (pharmacology), Enzyme-Linked Immunosorbent Assay (methods), Female, Humans, Intracellular Fluid (metabolism), Microscopy, Confocal (methods), PC12 Cells (drug effects), Potassium Chloride (pharmacology), Rats, Serum (metabolism).
- MESH :
- chemical , metabolism : Calcium.
- chemical , pharmacology : Antibodies, Complement System Proteins, Potassium Chloride.
- blood : Chorea.
- drug effects : PC12 Cells.
- immunology : Basal Ganglia, Chorea.
- metabolism : Intracellular Fluid, Serum.
- methods : Enzyme-Linked Immunosorbent Assay, Microscopy, Confocal.
- Adolescent, Animals, Child, Female, Humans, Rats.
Abstract
The proposed pathogenesis of Sydenham's chorea (SC) is an autoantibody-mediated basal ganglia dysfunction. Our study has shown that incubation of PC12 cells with complement-inactivated serum from SC patients was associated with a significant increase in Ca2+ levels evoked by KCl stimulus (mean +/- SEM, 341.0 +/- 8.7% of fluorescence intensity, arbitrary units) when compared with incubation with control serum (313.8 +/- 8.7% of fluorescence intensity, arbitrary units; P = 0.01). The increase in Ca2+ levels determined by SC patients sera correlated directly with the enzyme-linked immunosorbent assay optical density values for anti-basal ganglia antibodies. Our study supports the hypothesis that antibodies against basal ganglia in SC may cause their dysfunction.
DOI: 10.1002/mds.20418
PubMed: 15747354
Links to Exploration step
pubmed:15747354Le document en format XML
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<author><name sortKey="Teixeira, Antonio L" sort="Teixeira, Antonio L" uniqKey="Teixeira A" first="Antonio L" last="Teixeira">Antonio L. Teixeira</name>
<affiliation><nlm:affiliation>Movement Disorders Clinic, Hospital das Clínicas, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Guimaraes, Melissa M" sort="Guimaraes, Melissa M" uniqKey="Guimaraes M" first="Melissa M" last="Guimarães">Melissa M. Guimarães</name>
</author>
<author><name sortKey="Romano Silva, Marco Aurelio" sort="Romano Silva, Marco Aurelio" uniqKey="Romano Silva M" first="Marco Aurélio" last="Romano-Silva">Marco Aurélio Romano-Silva</name>
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<author><name sortKey="Cardoso, Francisco" sort="Cardoso, Francisco" uniqKey="Cardoso F" first="Francisco" last="Cardoso">Francisco Cardoso</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Serum from Sydenham's chorea patients modifies intracellular calcium levels in PC12 cells by a complement-independent mechanism.</title>
<author><name sortKey="Teixeira, Antonio L" sort="Teixeira, Antonio L" uniqKey="Teixeira A" first="Antonio L" last="Teixeira">Antonio L. Teixeira</name>
<affiliation><nlm:affiliation>Movement Disorders Clinic, Hospital das Clínicas, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.</nlm:affiliation>
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<author><name sortKey="Guimaraes, Melissa M" sort="Guimaraes, Melissa M" uniqKey="Guimaraes M" first="Melissa M" last="Guimarães">Melissa M. Guimarães</name>
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<author><name sortKey="Romano Silva, Marco Aurelio" sort="Romano Silva, Marco Aurelio" uniqKey="Romano Silva M" first="Marco Aurélio" last="Romano-Silva">Marco Aurélio Romano-Silva</name>
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<author><name sortKey="Cardoso, Francisco" sort="Cardoso, Francisco" uniqKey="Cardoso F" first="Francisco" last="Cardoso">Francisco Cardoso</name>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adolescent</term>
<term>Animals</term>
<term>Antibodies (pharmacology)</term>
<term>Basal Ganglia (immunology)</term>
<term>Calcium (metabolism)</term>
<term>Child</term>
<term>Chorea (blood)</term>
<term>Chorea (immunology)</term>
<term>Complement System Proteins (pharmacology)</term>
<term>Enzyme-Linked Immunosorbent Assay (methods)</term>
<term>Female</term>
<term>Humans</term>
<term>Intracellular Fluid (metabolism)</term>
<term>Microscopy, Confocal (methods)</term>
<term>PC12 Cells (drug effects)</term>
<term>Potassium Chloride (pharmacology)</term>
<term>Rats</term>
<term>Serum (metabolism)</term>
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<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Calcium</term>
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<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en"><term>Antibodies</term>
<term>Complement System Proteins</term>
<term>Potassium Chloride</term>
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<keywords scheme="MESH" qualifier="blood" xml:lang="en"><term>Chorea</term>
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<keywords scheme="MESH" qualifier="drug effects" xml:lang="en"><term>PC12 Cells</term>
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<keywords scheme="MESH" qualifier="immunology" xml:lang="en"><term>Basal Ganglia</term>
<term>Chorea</term>
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<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Intracellular Fluid</term>
<term>Serum</term>
</keywords>
<keywords scheme="MESH" qualifier="methods" xml:lang="en"><term>Enzyme-Linked Immunosorbent Assay</term>
<term>Microscopy, Confocal</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Adolescent</term>
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<front><div type="abstract" xml:lang="en">The proposed pathogenesis of Sydenham's chorea (SC) is an autoantibody-mediated basal ganglia dysfunction. Our study has shown that incubation of PC12 cells with complement-inactivated serum from SC patients was associated with a significant increase in Ca2+ levels evoked by KCl stimulus (mean +/- SEM, 341.0 +/- 8.7% of fluorescence intensity, arbitrary units) when compared with incubation with control serum (313.8 +/- 8.7% of fluorescence intensity, arbitrary units; P = 0.01). The increase in Ca2+ levels determined by SC patients sera correlated directly with the enzyme-linked immunosorbent assay optical density values for anti-basal ganglia antibodies. Our study supports the hypothesis that antibodies against basal ganglia in SC may cause their dysfunction.</div>
</front>
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<Day>13</Day>
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<ArticleTitle>Serum from Sydenham's chorea patients modifies intracellular calcium levels in PC12 cells by a complement-independent mechanism.</ArticleTitle>
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<Abstract><AbstractText>The proposed pathogenesis of Sydenham's chorea (SC) is an autoantibody-mediated basal ganglia dysfunction. Our study has shown that incubation of PC12 cells with complement-inactivated serum from SC patients was associated with a significant increase in Ca2+ levels evoked by KCl stimulus (mean +/- SEM, 341.0 +/- 8.7% of fluorescence intensity, arbitrary units) when compared with incubation with control serum (313.8 +/- 8.7% of fluorescence intensity, arbitrary units; P = 0.01). The increase in Ca2+ levels determined by SC patients sera correlated directly with the enzyme-linked immunosorbent assay optical density values for anti-basal ganglia antibodies. Our study supports the hypothesis that antibodies against basal ganglia in SC may cause their dysfunction.</AbstractText>
<CopyrightInformation>Copyright 2005 Movement Disorder Society.</CopyrightInformation>
</Abstract>
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<ForeName>Antonio L</ForeName>
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