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PMID: 15385607 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Tumor necrosis factor-like weak inducer of apoptosis-induced neurodegeneration.

Potrovita I, Zhang W, Burkly L, Hahm K, Lincecum J, Wang MZ, Maurer MH, Rossner M, Schneider A, Schwaninger M

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 properties in vivo and 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 ischemia in vivo or 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)-kappaB-luciferase fusion gene demonstrated that TWEAK stimulated transcriptional activity of NF-kappaB through Fn14 and the IkappaB kinase. Inhibition of NF-kappaB reduced TWEAK-stimulated neuronal cell death, suggesting that NF-kappaB 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 neurodegeneration in vivo.

MeSH Terms
Animals Antibodies/administration & dosage,pharmacology Apoptosis Regulatory Proteins Brain Ischemia/complications,metabolism,pathology Carrier Proteins/antagonists & inhibitors,genetics,metabolism Cell Death/genetics,physiology Cells, Cultured Cerebral Infarction/genetics,pathology,prevention & control Cytokine TWEAK Disease Models, Animal Gene Expression Profiling Humans I-kappa B Kinase Male Mice Mice, Inbred Strains Mice, Knockout NF-kappa B/biosynthesis,genetics Nerve Degeneration/etiology,metabolism,pathology Neurons/metabolism,pathology Protein Serine-Threonine Kinases/metabolism RNA/biosynthesis,genetics Receptors, Tumor Necrosis Factor/biosynthesis,genetics Recombinant Fusion Proteins/genetics,metabolism Stroke/complications,metabolism,pathology TWEAK Receptor Transfection Tumor Necrosis Factors Up-Regulation/genetics
Chemicals
Antibodies Apoptosis Regulatory Proteins Carrier Proteins Cytokine TWEAK NF-kappa B Receptors, Tumor Necrosis Factor Recombinant Fusion Proteins TNFRSF12A protein, human TNFSF12 protein, human TWEAK Receptor Tnfrsf12a protein, mouse Tumor Necrosis Factors RNA Protein Serine-Threonine Kinases CHUK protein, human Chuk protein, mouse I-kappa B Kinase IKBKB protein, human IKBKE protein, human Ikbkb protein, mouse Ikbke protein, mouse
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Potrovita Ioana
Department of Neurology, University of Heidelberg, D-69120 Heidelberg, Germany.
Zhang Wen
Burkly Linda
Hahm Kyungmin
Lincecum John
Wang Monica Z
Maurer Martin H
Rossner Moritz
Schneider Armin
Schwaninger Markus
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Article Info
Journal
The Journal of neuroscience : the official journal of the Society for Neuroscience
Abbr.
J Neurosci
ISSN
1529-2401
Published
2004-09-22
Pages
8237-44
Language
English
Region
United States
NLM ID
8102140
PMCID
PMC6729692
Subset
IM
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