## Abstract Understanding the regulation of cell death pathways is critical for protecting myelin‐producing cells and their associated axons during injury resulting from multiple sclerosis and other degenerative diseases. The immortalized N20.1 oligodendroglial cell line provides a useful model for
Lipopolysaccharide sensitizes microglia toward Ca2+-induced cell death: Mode of cell death shifts from apoptosis to necrosis
✍ Scribed by Takayuki Nagano; Shinya H. Kimura; Eri Takai; Toshio Matsuda; Motohiko Takemura
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 541 KB
- Volume
- 53
- Category
- Article
- ISSN
- 0894-1491
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Little is known about the effect of microglial activation on cell death. This study examines the effects of lipopolysaccharide (LPS) and interferon‐γ (IFN‐γ), triggers of microglial activation, on cell death induced by several agents in cultured rat microglia. For comparison, the effect of LPS on cell death is also examined in cultured astrocytes. LPS or IFN‐γ enhanced cell death induced by thapsigargin or ionomycin, an agent that increases intracellular Ca^2+^ concentration, although LPS or IFN‐γ alone did not affect cell viability. Thapsigargin or ionomycin induced apoptosis in LPS‐untreated microglia, while they induced necrosis in LPS‐treated microglia, which were partially reversed by O,O′‐bis(2‐aminophenyl)ethyleneglycol‐N,N,N′,N′‐tetraacetic acid tetraacetoxymethyl ester (BAPTA‐AM, an intracellular Ca^2+^ chelator). In contrast, LPS treatment did not affect tunicamycin‐ or staurosporine‐induced apoptosis, while it inhibited S‐nitroso‐N‐acetylpenicillamine‐induced apoptosis. The effect of LPS on thapsigargin or ionomycin‐induced apoptosis was not observed in astrocytes. These results indicate that microglial activation sensitizes the cells toward cell death induced by the change in intracellular Ca^2+^ concentration and shifts the mode of cell death from apoptosis to necrosis. © 2005 Wiley‐Liss, Inc.
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