001     137048
005     20240321220159.0
024 7 _ |a 10.1084/jem.20122143
|2 doi
024 7 _ |a pmid:23999498
|2 pmid
024 7 _ |a pmc:PMC3782053
|2 pmc
024 7 _ |a 0022-1007
|2 ISSN
024 7 _ |a 1540-9358
|2 ISSN
024 7 _ |a 1540-9538
|2 ISSN
037 _ _ |a DZNE-2020-03370
041 _ _ |a English
082 _ _ |a 610
100 1 _ |a Kreutzfeldt, Mario
|0 P:(DE-HGF)0
|b 0
245 _ _ |a Neuroprotective intervention by interferon-γ blockade prevents CD8+ T cell-mediated dendrite and synapse loss.
260 _ _ |a New York, NY
|c 2013
|b Rockefeller Univ. Press
264 _ 1 |3 online
|2 Crossref
|b Rockefeller University Press
|c 2013-09-02
264 _ 1 |3 print
|2 Crossref
|b Rockefeller University Press
|c 2013-09-23
336 7 _ |a article
|2 DRIVER
336 7 _ |a Output Types/Journal article
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336 7 _ |a Journal Article
|b journal
|m journal
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|s 1588243704_17523
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336 7 _ |a ARTICLE
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336 7 _ |a JOURNAL_ARTICLE
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336 7 _ |a Journal Article
|0 0
|2 EndNote
520 _ _ |a Neurons are postmitotic and thus irreplaceable cells of the central nervous system (CNS). Accordingly, CNS inflammation with resulting neuronal damage can have devastating consequences. We investigated molecular mediators and structural consequences of CD8(+) T lymphocyte (CTL) attack on neurons in vivo. In a viral encephalitis model in mice, disease depended on CTL-derived interferon-γ (IFN-γ) and neuronal IFN-γ signaling. Downstream STAT1 phosphorylation and nuclear translocation in neurons were associated with dendrite and synapse loss (deafferentation). Analogous molecular and structural alterations were also found in human Rasmussen encephalitis, a CTL-mediated human autoimmune disorder of the CNS. Importantly, therapeutic intervention by IFN-γ blocking antibody prevented neuronal deafferentation and clinical disease without reducing CTL responses or CNS infiltration. These findings identify neuronal IFN-γ signaling as a novel target for neuroprotective interventions in CTL-mediated CNS disease.
536 _ _ |a 341 - Molecular Signaling (POF3-341)
|0 G:(DE-HGF)POF3-341
|c POF3-341
|f POF III
|x 0
588 _ _ |a Dataset connected to CrossRef, PubMed,
650 _ 7 |a Receptors, Interferon
|2 NLM Chemicals
650 _ 7 |a STAT1 Transcription Factor
|2 NLM Chemicals
650 _ 7 |a fas Receptor
|2 NLM Chemicals
650 _ 7 |a interferon gamma receptor
|0 07MXG07O12
|2 NLM Chemicals
650 _ 7 |a Perforin
|0 126465-35-8
|2 NLM Chemicals
650 _ 7 |a Interferon-gamma
|0 82115-62-6
|2 NLM Chemicals
650 _ 2 |a Adolescent
|2 MeSH
650 _ 2 |a Adult
|2 MeSH
650 _ 2 |a Animals
|2 MeSH
650 _ 2 |a CD8-Positive T-Lymphocytes: immunology
|2 MeSH
650 _ 2 |a Cell Nucleus: metabolism
|2 MeSH
650 _ 2 |a Child
|2 MeSH
650 _ 2 |a Dendrites: immunology
|2 MeSH
650 _ 2 |a Humans
|2 MeSH
650 _ 2 |a Interferon-gamma: antagonists & inhibitors
|2 MeSH
650 _ 2 |a Interferon-gamma: metabolism
|2 MeSH
650 _ 2 |a Lymphocytic Choriomeningitis: immunology
|2 MeSH
650 _ 2 |a Lymphocytic Choriomeningitis: metabolism
|2 MeSH
650 _ 2 |a Lymphocytic Choriomeningitis: prevention & control
|2 MeSH
650 _ 2 |a Lymphocytic choriomeningitis virus: immunology
|2 MeSH
650 _ 2 |a Mice
|2 MeSH
650 _ 2 |a Mice, Transgenic
|2 MeSH
650 _ 2 |a Neurons: immunology
|2 MeSH
650 _ 2 |a Neurons: metabolism
|2 MeSH
650 _ 2 |a Neurons: virology
|2 MeSH
650 _ 2 |a Perforin: genetics
|2 MeSH
650 _ 2 |a Perforin: metabolism
|2 MeSH
650 _ 2 |a Phosphorylation
|2 MeSH
650 _ 2 |a Protein Transport
|2 MeSH
650 _ 2 |a Receptors, Interferon: genetics
|2 MeSH
650 _ 2 |a Receptors, Interferon: metabolism
|2 MeSH
650 _ 2 |a STAT1 Transcription Factor: metabolism
|2 MeSH
650 _ 2 |a Signal Transduction
|2 MeSH
650 _ 2 |a Spinal Cord: immunology
|2 MeSH
650 _ 2 |a Spinal Cord: metabolism
|2 MeSH
650 _ 2 |a Spinal Cord: pathology
|2 MeSH
650 _ 2 |a Synapses: immunology
|2 MeSH
650 _ 2 |a T-Lymphocytes, Cytotoxic: immunology
|2 MeSH
650 _ 2 |a Young Adult
|2 MeSH
650 _ 2 |a fas Receptor: genetics
|2 MeSH
650 _ 2 |a fas Receptor: metabolism
|2 MeSH
700 1 _ |a Bergthaler, Andreas
|0 P:(DE-HGF)0
|b 1
700 1 _ |a Fernandez, Marylise
|0 P:(DE-HGF)0
|b 2
700 1 _ |a Brück, Wolfgang
|0 P:(DE-HGF)0
|b 3
700 1 _ |a Steinbach, Karin
|0 P:(DE-HGF)0
|b 4
700 1 _ |a Vorm, Mariann
|0 P:(DE-HGF)0
|b 5
700 1 _ |a Coras, Roland
|0 P:(DE-HGF)0
|b 6
700 1 _ |a Blümcke, Ingmar
|0 P:(DE-HGF)0
|b 7
700 1 _ |a Bonilla, Weldy V
|0 P:(DE-HGF)0
|b 8
700 1 _ |a Fleige, Anne
|0 P:(DE-HGF)0
|b 9
700 1 _ |a Forman, Ruth
|0 P:(DE-HGF)0
|b 10
700 1 _ |a Müller, Werner
|0 P:(DE-HGF)0
|b 11
700 1 _ |a Becher, Burkhard
|0 P:(DE-HGF)0
|b 12
700 1 _ |a Misgeld, Thomas
|0 P:(DE-2719)2810727
|b 13
|u dzne
700 1 _ |a Kerschensteiner, Martin
|0 P:(DE-HGF)0
|b 14
700 1 _ |a Pinschewer, Daniel D
|0 P:(DE-HGF)0
|b 15
700 1 _ |a Merkler, Doron
|0 P:(DE-HGF)0
|b 16
|e Corresponding author
773 1 8 |a 10.1084/jem.20122143
|b : Rockefeller University Press, 2013-09-02
|n 10
|p 2087-2103
|3 journal-article
|2 Crossref
|t The Journal of Experimental Medicine
|v 210
|y 2013
|x 1540-9538
773 _ _ |a 10.1084/jem.20122143
|g Vol. 210, no. 10, p. 2087 - 2103
|0 PERI:(DE-600)1477240-1
|n 10
|q 210:10<2087 - 2103
|p 2087-2103
|t Journal of experimental medicine
|v 210
|y 2013
|x 1540-9538
856 7 _ |2 Pubmed Central
|u http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3782053
909 C O |o oai:pub.dzne.de:137048
|p VDB
910 1 _ |a Deutsches Zentrum für Neurodegenerative Erkrankungen
|0 I:(DE-588)1065079516
|k DZNE
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913 1 _ |a DE-HGF
|b Forschungsbereich Gesundheit
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914 1 _ |y 2013
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LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21