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Human ApoD an apolipoprotein up-regulated in neurodegenerative diseases extends lifespan and increases stress resistance in Drosophila

机译:人ApoD是一种在神经退行性疾病中上调的载脂蛋白可延长果蝇的寿命并提高其抗逆性

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摘要

Apolipoprotein D (ApoD) expression increases in several neurological disorders and in spinal cord injury. We provide a report of a physiological role for human ApoD (hApoD): Flies overexpressing hApoD are long-lived and protected against stress conditions associated with aging and neurodegeneration, including hyperoxia, dietary paraquat, and heat stress. We show that the fly ortholog, Glial Lazarillo, is strongly up-regulated in response to these extrinsic stresses and also can protect in vitro-cultured cells in situations modeling Alzheimer's disease (AD) and Parkinson's disease (PD). In adult flies, hApoD overexpression reduces age-associated lipid peroxide accumulation, suggesting a proximal mechanism of action. Similar data obtained in the mouse [Ganfornina, M.D., et al., (2008) Apolipoprotein D is involved in the mechanisms regulating protection from oxidative stress. Aging Cell 10.1111/j.1474-9726.2008.00395.] as well as in plants (Charron et al., personal communication) suggest that ApoD and its orthologs play an evolutionarily conserved role in response to stress, possibly managing or preventing lipid peroxidation.
机译:在一些神经系统疾病和脊髓损伤中,载脂蛋白D(ApoD)的表达增加。我们提供了有关人类ApoD(hApoD)的生理作用的报告:过表达hApoD的果蝇是长寿的,可以抵御与衰老和神经退行性变有关的应激条件,包括高氧血症,饮食百草枯和热应激。我们显示苍蝇直向同源物,胶质Lazarillo,强烈响应这些外在压力上调,并且还可以在建模阿尔茨海默氏病(AD)和帕金森氏病(PD)的情况下保护体外培养的细胞。在成年果蝇中,hApoD的过度表达减少了与年龄相关的脂质过氧化物的积累,表明了近端的作用机制。在小鼠中获得的相似数据[Ganfornina,M.D。等人,(2008)载脂蛋白D参与调节保护免受氧化应激的机制。 [Aging Cell 10.1111 / j.1474-9726.2008.00395。]以及在植物中(Charron等人,个人交流)表明,ApoD及其直系同源物在对压力的响应中起进化上保守的作用,可能控制或预防脂质过氧化。

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