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Journal of Neuroscience
Article . 2004 . Peer-reviewed
License: CC BY NC SA
Data sources: Crossref
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Tumor Necrosis Factor-Like Weak Inducer of Apoptosis-Induced Neurodegeneration

Authors: Kyungmin Hahm; John Lincecum; Monica Z. Wang; Markus Schwaninger; Moritz J. Rossner; Ioana Potrovita; Wen Zhang; +3 Authors

Tumor Necrosis Factor-Like Weak Inducer of Apoptosis-Induced Neurodegeneration

Abstract

Tumor necrosis factor-like weak inducer of apoptosis (TWEAK) is a member of the tumor necrosis factor (TNF) family of cytokines. It has proangiogenic and proinflammatory propertiesin vivoand induces cell death in tumor cell lines. TWEAK effects are mediated by the membrane receptor Fn14. In a systematic search for genes regulated in a murine stroke model with the tag-sequencing technique massively parallel signature sequencing, we have identified TWEAK as an induced gene. After 24 hr of focal cerebral ischemiain vivoor oxygen glucose deprivation in primary cortical neurons, both TWEAK and its receptor Fn14 were significantly upregulated. TWEAK induced cell death in primary neurons. Transfection of a nuclear factor (NF)-κB-luciferase fusion gene demonstrated that TWEAK stimulated transcriptional activity of NF-κB through Fn14 and the IκB kinase. Inhibition of NF-κB reduced TWEAK-stimulated neuronal cell death, suggesting that NF-κB mediates TWEAK-induced neurodegeneration at least in part. Intraperitoneal injection of a neutralizing anti-TWEAK antibody significantly reduced the infarct size after 48 hr of permanent cerebral ischemia. In summary, our data show that TWEAK induces neuronal cell death and is involved in neurodegenerationin vivo.

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Keywords

Male, Mice, Knockout, Neurons, Cell Death, Gene Expression Profiling, NF-kappa B, Cytokine TWEAK, Mice, Inbred Strains, Cerebral Infarction, Antibodies, Brain Ischemia, I-kappa B Kinase, Disease Models, Animal, Mice, Nerve Degeneration, Animals, Humans, Apoptosis Regulatory Proteins, Carrier Proteins, Cells, Cultured

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    This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    124
    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
    Top 10%
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    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
    Top 10%
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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
124
Top 10%
Top 10%
Top 10%
hybrid