Guo Jun Tang, Chen An Qi, Kong Qi, Zhu Hua, Ma Chun Mei, Qin Chuan
Institute of Laboratory Animal Sciences, Chinese Academy of Medical Sciences, Peking Union Medical College, 5 Panjiayuannanli, Beijing, 100021, China.
Cell Mol Neurobiol. 2008 Jan;28(1):35-47. doi: 10.1007/s10571-007-9227-0. Epub 2007 Nov 6.
alpha-Synuclein plays a key role in the pathological neurodegeneration in Parkinson's disease. Although its contribution to normal physiology remains elusive, the selective degeneration of alpha-synuclein-containing dopaminergic neurons in Parkinson's disease may be linked to abnormal alpha-synuclein induced toxicity. In the present study, a complex of alpha-synuclein and vesicular monoamine transporter-2 was identified by GST-Pull Down experiment. In wild-type alpha-synuclein stably transfected SH-SY5Y cell lines, the activity of vesicular monoamine transporter-2 decreased by 31% as determined by [(3)H] dopamine uptake, and its expression also decreased in both protein and mRNA levels using western and northern blot analysis. Overexpression of wild-type alpha-synuclein did not induce cell death or apoptosis, but significantly enhanced the intracellular reactive oxygen species level as assayed by flow cytometry. These data suggest that Up-regulated alpha-synuclein expression inhibits the activity of vesicular monoamine transporter-2, thereby interrupting dopamine homeostasis and resulting in dopaminergic neuron injury in Parkinson's disease.
α-突触核蛋白在帕金森病的病理性神经退行性变中起关键作用。尽管其对正常生理功能的贡献仍不清楚,但帕金森病中含α-突触核蛋白的多巴胺能神经元的选择性变性可能与异常α-突触核蛋白诱导的毒性有关。在本研究中,通过GST下拉实验鉴定了α-突触核蛋白与囊泡单胺转运体2的复合物。在稳定转染野生型α-突触核蛋白的SH-SY5Y细胞系中,通过[³H]多巴胺摄取测定,囊泡单胺转运体2的活性降低了31%,并且使用蛋白质印迹和Northern印迹分析,其在蛋白质和mRNA水平的表达也降低。野生型α-突触核蛋白的过表达未诱导细胞死亡或凋亡,但通过流式细胞术检测,显著提高了细胞内活性氧水平。这些数据表明,α-突触核蛋白表达上调抑制囊泡单胺转运体2的活性,从而破坏多巴胺稳态并导致帕金森病中的多巴胺能神经元损伤。