Cytotoxicity in cytokine stimulated astrocyte cultures: Role of IL-6 and nitric oxide
Makaleler > Tam Makale · 2004
Yazarlar: Özlem YILMAZ, Dilek TAŞKIRAN, S AYDAR
NEUROSCIENCE RESEARCH COMMUNICATIONS, SCI Expanded İndekslerine Giren Dergi, Uluslararası, 2004, cilt 34, ss 82-91
DOI: 10.1002/nrc.20002
Özet
The cytokines interleukin 1 (IL-1) and tumor necrosis factor alpha (TNF-alpha), produced by glial cells within the brain, appear to contribute to the neuropathogenesis of several inflammatory neurodegenerative diseases. However, little is known about the mechanism underlying cytokine-induced neurotoxicity. Using astroglial cultures obtained from fetal rat brain, we investigated the effects of lipopolysacchanides (LPS) and cytokines (IL-1beta and TNF-alpha). Primary cell cultures treated with LPS, IL-1beta plus TNF-alpha generated substantial amounts of nitric oxide (NO), elevated interleukin 6 (IL-6) levels and caused astroglial injury measured by lactate dehydrogenase (LDH) activity. However, blockade of NO production with nitric oxide synthase (NOS) inhibitors did not affect cell death, suggesting that NO is not responsible for cytokine-induced astroglial cell death under the experimental conditions employed.