IgG Isolated from LP-BM5 Infected Mouse Brain Activates Ionotropic Glutamate Receptors
Biochemical and immunological studies have shown that mice infected with LP-BM5 virus develop antibodies to ionotropic glutamate receptors. Here, IgG isolated from brain of infected mice has been tested electrophysiologically on cultured rat cortical and hippocampal neurons. The IgG elicited glycine...
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doaj-42616dc36a624019861339009b9581702021-03-20T04:47:21ZengElsevierNeurobiology of Disease1095-953X2001-12-018610691081IgG Isolated from LP-BM5 Infected Mouse Brain Activates Ionotropic Glutamate ReceptorsAnthony S. Basile0Elena Koustova1P. Ioan2S. Rizzoli3Michael A. Rogawski4Peter N.R. Usherwood5Laboratory of Bioorganic Chemistry, NIDDKD, National Institutes of Health, Bethesda, Maryland, 20892; Epilepsy Research Branch, NINDS, National Institutes of Health, Bethesda, Maryland, 20892; Division of Molecular Toxicology, School of Life and Environmental Sciences, University Park, University of Nottingham, Nottingham, NG7 2RD, United KingdomLaboratory of Bioorganic Chemistry, NIDDKD, National Institutes of Health, Bethesda, Maryland, 20892; Epilepsy Research Branch, NINDS, National Institutes of Health, Bethesda, Maryland, 20892; Division of Molecular Toxicology, School of Life and Environmental Sciences, University Park, University of Nottingham, Nottingham, NG7 2RD, United KingdomLaboratory of Bioorganic Chemistry, NIDDKD, National Institutes of Health, Bethesda, Maryland, 20892; Epilepsy Research Branch, NINDS, National Institutes of Health, Bethesda, Maryland, 20892; Division of Molecular Toxicology, School of Life and Environmental Sciences, University Park, University of Nottingham, Nottingham, NG7 2RD, United KingdomLaboratory of Bioorganic Chemistry, NIDDKD, National Institutes of Health, Bethesda, Maryland, 20892; Epilepsy Research Branch, NINDS, National Institutes of Health, Bethesda, Maryland, 20892; Division of Molecular Toxicology, School of Life and Environmental Sciences, University Park, University of Nottingham, Nottingham, NG7 2RD, United KingdomLaboratory of Bioorganic Chemistry, NIDDKD, National Institutes of Health, Bethesda, Maryland, 20892; Epilepsy Research Branch, NINDS, National Institutes of Health, Bethesda, Maryland, 20892; Division of Molecular Toxicology, School of Life and Environmental Sciences, University Park, University of Nottingham, Nottingham, NG7 2RD, United KingdomLaboratory of Bioorganic Chemistry, NIDDKD, National Institutes of Health, Bethesda, Maryland, 20892; Epilepsy Research Branch, NINDS, National Institutes of Health, Bethesda, Maryland, 20892; Division of Molecular Toxicology, School of Life and Environmental Sciences, University Park, University of Nottingham, Nottingham, NG7 2RD, United KingdomBiochemical and immunological studies have shown that mice infected with LP-BM5 virus develop antibodies to ionotropic glutamate receptors. Here, IgG isolated from brain of infected mice has been tested electrophysiologically on cultured rat cortical and hippocampal neurons. The IgG elicited glycine-independent currents that reversed at ∼0 mV. Equivalent concentrations of IgG from uninfected mice were inactive. The glycine-independent currents were less influenced by DNQX and GYKI-52466 than currents elicited by AMPA and KA. The IgG also elicited glycine-dependent currents that reversed at −10 mV and were blocked by dl-AP5, 5,7-DCKA, and polyamine amides. Glycine-dependent and -independent currents were unaffected by tetrodotoxin, strychnine, the transmembrane Cl− gradient or d-tubocurare. Although part of the glycine-independent current remains uncharacterized, these results confirm that a virus-induced immunopathology produces IgG clones that activate ionotropic glutamate receptors and that could, thereby, contribute to the excitotoxic neurological syndrome observed in LP-BM5-infected mice.http://www.sciencedirect.com/science/article/pii/S0969996101904425 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Anthony S. Basile Elena Koustova P. Ioan S. Rizzoli Michael A. Rogawski Peter N.R. Usherwood |
spellingShingle |
Anthony S. Basile Elena Koustova P. Ioan S. Rizzoli Michael A. Rogawski Peter N.R. Usherwood IgG Isolated from LP-BM5 Infected Mouse Brain Activates Ionotropic Glutamate Receptors Neurobiology of Disease |
author_facet |
Anthony S. Basile Elena Koustova P. Ioan S. Rizzoli Michael A. Rogawski Peter N.R. Usherwood |
author_sort |
Anthony S. Basile |
title |
IgG Isolated from LP-BM5 Infected Mouse Brain Activates Ionotropic Glutamate Receptors |
title_short |
IgG Isolated from LP-BM5 Infected Mouse Brain Activates Ionotropic Glutamate Receptors |
title_full |
IgG Isolated from LP-BM5 Infected Mouse Brain Activates Ionotropic Glutamate Receptors |
title_fullStr |
IgG Isolated from LP-BM5 Infected Mouse Brain Activates Ionotropic Glutamate Receptors |
title_full_unstemmed |
IgG Isolated from LP-BM5 Infected Mouse Brain Activates Ionotropic Glutamate Receptors |
title_sort |
igg isolated from lp-bm5 infected mouse brain activates ionotropic glutamate receptors |
publisher |
Elsevier |
series |
Neurobiology of Disease |
issn |
1095-953X |
publishDate |
2001-12-01 |
description |
Biochemical and immunological studies have shown that mice infected with LP-BM5 virus develop antibodies to ionotropic glutamate receptors. Here, IgG isolated from brain of infected mice has been tested electrophysiologically on cultured rat cortical and hippocampal neurons. The IgG elicited glycine-independent currents that reversed at ∼0 mV. Equivalent concentrations of IgG from uninfected mice were inactive. The glycine-independent currents were less influenced by DNQX and GYKI-52466 than currents elicited by AMPA and KA. The IgG also elicited glycine-dependent currents that reversed at −10 mV and were blocked by dl-AP5, 5,7-DCKA, and polyamine amides. Glycine-dependent and -independent currents were unaffected by tetrodotoxin, strychnine, the transmembrane Cl− gradient or d-tubocurare. Although part of the glycine-independent current remains uncharacterized, these results confirm that a virus-induced immunopathology produces IgG clones that activate ionotropic glutamate receptors and that could, thereby, contribute to the excitotoxic neurological syndrome observed in LP-BM5-infected mice. |
url |
http://www.sciencedirect.com/science/article/pii/S0969996101904425 |
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