Wang Yi-Min, Pu Pu, Le Wei-Dong
Neural Genomics Laboratory, Institute of Health Sciences, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences/Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.
Neurosci Bull. 2007 Nov;23(6):329-35. doi: 10.1007/s12264-007-0049-3.
To investigate the toxic effect of environmental neurotoxin MPP+ to C. elegans and identify the mechanisms that cause the toxicity.
Human alpha-synuclein transgenic C. elegans was used as the animal model, the toxic effect of MPP+ to dopamine (DA) neurons and the lifespan of worms was tested. The worms were feed with OP50 to determine whether ATP increase can rescue the worm from toxicity. ATP level and aberrant protein accumulation were analyzed in the MPP+ treated worms with or without OP50 addition.
We found that MPP+ induced DA cell death and worm lethality, which could be prevented by OP50 treatment. OP50 exerted the protective effect by up-regulating ATP level, even though it also induced accumulation of alpha-synuclein. Despite the undefined role of protein aggregation to the cell death, our results showed that the toxicity of MPP+ was mainly caused by the ATP depletion in the alpha-synuclein transgenic C. elegans.
MPP+ could induce DA neuronal death and worm lethality in alpha-synuclein transgenic C. elegans; Compared with the aggregation of alpha-synuclein, the major cause of MPP+ toxicity appeared due to ATP depletion.
研究环境神经毒素MPP+对秀丽隐杆线虫的毒性作用,并确定其毒性产生的机制。
以人α-突触核蛋白转基因秀丽隐杆线虫作为动物模型,检测MPP+对多巴胺(DA)神经元的毒性作用及线虫的寿命。用OP50喂养线虫,以确定ATP增加是否能使线虫免受毒性影响。分析添加或不添加OP50的情况下,经MPP+处理的线虫的ATP水平和异常蛋白积累情况。
我们发现MPP+可诱导DA细胞死亡和线虫致死,而OP50处理可预防这种情况。OP50通过上调ATP水平发挥保护作用,尽管它也会诱导α-突触核蛋白的积累。尽管蛋白质聚集对细胞死亡的作用尚不明确,但我们的结果表明,MPP+的毒性主要是由α-突触核蛋白转基因秀丽隐杆线虫中的ATP耗竭引起的。
MPP+可诱导α-突触核蛋白转基因秀丽隐杆线虫中的DA神经元死亡和线虫致死;与α-突触核蛋白的聚集相比,MPP+毒性的主要原因似乎是ATP耗竭。