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Reduced Immunoproteasome Formation and Accumulation of Immunoproteasomal Precursors in the Brains of Lymphocytic Choriomeningitis Virus-Infected Mice

Reduced Immunoproteasome Formation and Accumulation of Immunoproteasomal Precursors in the Brains of Lymphocytic Choriomeningitis Virus-Infected Mice

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KREMER, Marcel, Anja HENN, Cornelia KOLB, Michael BASLER, Jacqueline MOEBIUS, Benoît GUILLAUME, Marcel LEIST, Benoît J. van den EYNDE, Marcus GRÖTTRUP, 2010. Reduced Immunoproteasome Formation and Accumulation of Immunoproteasomal Precursors in the Brains of Lymphocytic Choriomeningitis Virus-Infected Mice. In: The Journal of Immunology. 185(9), pp. 5549-5560. ISSN 0022-1767. eISSN 1550-6606

@article{Kremer2010-11-01Reduc-12520, title={Reduced Immunoproteasome Formation and Accumulation of Immunoproteasomal Precursors in the Brains of Lymphocytic Choriomeningitis Virus-Infected Mice}, year={2010}, doi={10.4049/jimmunol.1001517}, number={9}, volume={185}, issn={0022-1767}, journal={The Journal of Immunology}, pages={5549--5560}, author={Kremer, Marcel and Henn, Anja and Kolb, Cornelia and Basler, Michael and Moebius, Jacqueline and Guillaume, Benoît and Leist, Marcel and Eynde, Benoît J. van den and Gröttrup, Marcus} }

<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:bibo="http://purl.org/ontology/bibo/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:xsd="http://www.w3.org/2001/XMLSchema#" > <rdf:Description rdf:about="https://kops.uni-konstanz.de/rdf/resource/123456789/12520"> <dc:rights>deposit-license</dc:rights> <dc:creator>Henn, Anja</dc:creator> <dc:creator>Guillaume, Benoît</dc:creator> <dc:contributor>Eynde, Benoît J. van den</dc:contributor> <dc:contributor>Kolb, Cornelia</dc:contributor> <dc:creator>Leist, Marcel</dc:creator> <dc:contributor>Moebius, Jacqueline</dc:contributor> <bibo:uri rdf:resource="http://kops.uni-konstanz.de/handle/123456789/12520"/> <dc:creator>Basler, Michael</dc:creator> <dc:creator>Kolb, Cornelia</dc:creator> <dc:contributor>Gröttrup, Marcus</dc:contributor> <dcterms:rights rdf:resource="http://nbn-resolving.org/urn:nbn:de:bsz:352-20140905103605204-4002607-1"/> <dc:contributor>Basler, Michael</dc:contributor> <dc:contributor>Guillaume, Benoît</dc:contributor> <dcterms:issued>2010-11-01</dcterms:issued> <dc:language>eng</dc:language> <dcterms:title>Reduced Immunoproteasome Formation and Accumulation of Immunoproteasomal Precursors in the Brains of Lymphocytic Choriomeningitis Virus-Infected Mice</dcterms:title> <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2011-06-20T09:32:03Z</dc:date> <dc:contributor>Henn, Anja</dc:contributor> <dc:creator>Gröttrup, Marcus</dc:creator> <dcterms:bibliographicCitation>First publ. in: Journal of Immunology ; 185 (2010), 9. - pp. 5549-5560</dcterms:bibliographicCitation> <dc:creator>Kremer, Marcel</dc:creator> <dc:creator>Eynde, Benoît J. van den</dc:creator> <dc:contributor>Kremer, Marcel</dc:contributor> <dc:contributor>Leist, Marcel</dc:contributor> <dc:creator>Moebius, Jacqueline</dc:creator> <dcterms:abstract xml:lang="eng">Tissue inflammation is accompanied by the cytokine-mediated replacement of constitutive proteasomes by immunoproteasomes that finally leads to an optimized generation of MHC class I restricted epitopes for Ag presentation. The brain is considered an immunoprivileged organ, where both the special anatomy as well as active tolerance mechanisms repress the development of inflammatory responses and help to prevent immunopathological damage. We analyzed the immunoproteasome expression in the brain after an infection with lymphocytic choriomeningitis virus (LCMV) and could show that LCMV-infection of mice leads to the transcriptional induction of inducible proteasome subunits in the brain. However, compared with other organs, i.p. and even intracranial infection with LCMV only led to a faint expression of mature immunoproteasome in the brain and resulted in the accumulation of immunoproteasomal precursors. By immunohistology, we could identify microglia-like cells as the main producers of immunoproteasome, whereas in astrocytes immunoproteasome expression was almost exclusively restricted to nuclei. Neither the immunoproteasome subunits low molecular mass polypeptide 2 nor multicatalytic endopeptidase complex-like–1 were detected in neurons or oligodendrocytes. In vitro studies of IFN-γ–stimulated primary astrocytes suggested that the observed accumulation of immunoproteasomal precursor complexes takes place in this cell population. Functionally, the lack of immunoproteasomes protracted and lowered the severity of LCMV-induced meningitis in LMP7−/− mice suggesting a contribution of immunoproteasomes in microglia to exacerbate immunopathological damage. We postulate a posttranslationally regulated mechanism that prevents abundant and inappropriate immunoproteasome assembly in the brain and may contribute to the protection of poorly regenerating cells of the CNS from immunopathological destruction.</dcterms:abstract> <dcterms:available rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2011-06-20T09:32:03Z</dcterms:available> </rdf:Description> </rdf:RDF>

Dateiabrufe seit 01.10.2014 (Informationen über die Zugriffsstatistik)

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