Non-fibrillar ¥â-amyloid exerts toxic effect on neuronal cells
±èÇöÁø, È«¼ºÃâ,
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±èÇöÁø ( Kim Hyeon-Jin ) - Jinis Biopharmaceuticals Co.
È«¼ºÃâ ( Hong Seong-Tshool ) - Jeonbuk National University Medical School Institute of Cardiovascular Research
Abstract
Alzheimer's disease is the most common form of dementia and no cure is known so far. Extensive genetic works and in vitro experiments combined with clinical observations link amyloid ¥â?protein (A¥â) to the pathogenesis of Alzheimer's disease (AD). It was hypothesized that A¥â becomes toxic when it adopts a fibrillar conformation. Recently, non?fibrillar form of A¥â was observed and the potential role in the pathogenesis of AD became an interesting subject. In this study, the cytotoxicity of non?fibrillar A¥â and fibrillar A¥â was compared on oxidative stress, membrane damage, or nucleosome break down. Non?fibrillar A¥â was not toxic in peripheral nervous system?derived cells but significantly toxic in central nervous system?derived cells while fibrillar A¥â was non?selectively toxic in both cell culture. The neurotoxicity of non?fibrillar A¥â was reproduced in semi?in vivo culture of mouse brain slice. In conclusion, non?fibrillar A¥â could be more relevant to the selective neurodegeneration in Alzheimer's brains than fibrillar A¥â and further research needs to be done for identification of the cause of AD.
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Alzheimer's disease; ¥â-Amyloid; NT2; SHSY5Y; Slice; Neurotoxicity
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