ACS Chem Neurosci. 2010 Mar 17;1(3):194-203. doi: 10.1021/cn900021z. Epub 2009 Dec 17.
Chronic exposure to manganese results in neurological symptoms referred to as manganism and is identified as a risk factor for Parkinson's disease. In vitro, manganese induces cell death in the dopaminergic cells, but the mechanisms of manganese cytotoxicity are still unexplained. In particular, the subcellular distribution of manganese and its interaction with other trace elements needed to be assessed. Applying synchrotron X-ray fluorescence nanoimaging, we found that manganese was located within the Golgi apparatus of PC12 dopaminergic cells at physiologic concentrations. At increasing concentrations, manganese accumulates within the Golgi apparatus until cytotoxic concentrations are reached resulting in a higher cytoplasmic content probably after the Golgi apparatus storage capacity is exceeded. Cell exposure to manganese and brefeldin A, a molecule known to specifically cause the collapse of the Golgi apparatus, results in the striking intracellular redistribution of manganese, which accumulates in the cytoplasm and the nucleus. These results indicate that the Golgi apparatus plays an important role in the cellular detoxification of manganese. In addition manganese exposure induces a decrease in total iron content, which could contribute to the overall neurotoxicity.
慢性锰暴露会导致神经症状,称为锰中毒,被认为是帕金森病的一个危险因素。在体外,锰会诱导多巴胺能细胞死亡,但锰细胞毒性的机制仍不清楚。特别是需要评估锰的亚细胞分布及其与其他必需微量元素的相互作用。应用同步加速器 X 射线荧光纳米成像技术,我们发现锰在生理浓度下位于 PC12 多巴胺能细胞的高尔基体中。随着浓度的增加,锰在高尔基体中积累,直到达到细胞毒性浓度,导致细胞质内容物升高,可能是高尔基体的储存容量超过之后的结果。细胞暴露于锰和布雷菲德菌素 A(一种已知可特异性导致高尔基体崩溃的分子)会导致锰在细胞内的显著重新分布,锰在细胞质和核内积累。这些结果表明高尔基体在锰的细胞解毒中起着重要作用。此外,锰暴露会诱导总铁含量的减少,这可能导致整体神经毒性。