Swerdlow R H, Parks J K, Cassarino D S, Binder D R, Bennett J P, Di Iorio G, Golbe L I, Parker W D
Center for the Study of Neurodegenerative Diseases, University of Virginia Health System, Charlottesville, Virginia, USA.
Exp Neurol. 2001 Jun;169(2):479-85. doi: 10.1006/exnr.2001.7674.
Complex I activity is reduced in cytoplasmic hybrid (cybrid) cell lines that contain mitochondrial DNA (mtDNA) from sporadic Parkinson's disease (PD) patients. This implies that mtDNA aberration occurs in sporadic PD. To assess the integrity of mtDNA in autosomal dominant PD arising from mutation of the alpha-synuclein gene, we transferred mitochondrial genes from PD-affected members of the Italian-American Contursi kindred to cells previously depleted of their endogenous mtDNA. Unlike cybrid cell lines expressing mtDNA from persons with sporadic or maternally inherited PD, the resultant Contursi cybrid lines did not manifest complex I deficiency, indicating that in Contursi PD mtDNA integrity is relatively preserved. Compared to control cybrids, however, Contursi cybrid lines did show some evidence of oxidative stress. For reasons that are unclear, at least a limited amount of mtDNA damage may nevertheless develop in PD patients with alpha-synuclein mutation.
在含有散发性帕金森病(PD)患者线粒体DNA(mtDNA)的细胞质杂种(cybrid)细胞系中,复合体I活性降低。这意味着散发性PD中发生了mtDNA畸变。为了评估由α-突触核蛋白基因突变引起的常染色体显性PD中mtDNA的完整性,我们将来自意大利裔美国人孔图尔西家族受PD影响成员的线粒体基因转移到先前已耗尽其内源性mtDNA的细胞中。与表达散发性或母系遗传性PD患者mtDNA的cybrid细胞系不同,所得的孔图尔西cybrid细胞系未表现出复合体I缺陷,这表明在孔图尔西PD中mtDNA完整性相对得以保留。然而,与对照cybrid相比,孔图尔西cybrid细胞系确实显示出一些氧化应激的证据。由于尚不清楚的原因,在具有α-突触核蛋白突变的PD患者中,至少可能会发生有限程度的mtDNA损伤。