Exner Nicole, Treske Bettina, Paquet Dominik, Holmström Kira, Schiesling Carola, Gispert Suzana, Carballo-Carbajal Iria, Berg Daniela, Hoepken Hans-Hermann, Gasser Thomas, Krüger Rejko, Winklhofer Konstanze F, Vogel Frank, Reichert Andreas S, Auburger Georg, Kahle Philipp J, Schmid Bettina, Haass Christian
Center for Integrated Protein Science Munich and Adolf-Butenandt-Institute, Department of Biochemistry, Laboratory for Alzheimer's and Parkinson's Disease Research, Ludwig-Maximilians-University, 80336 Munich, Germany.
J Neurosci. 2007 Nov 7;27(45):12413-8. doi: 10.1523/JNEUROSCI.0719-07.2007.
Degeneration of dopaminergic neurons in the substantia nigra is characteristic for Parkinson's disease (PD), the second most common neurodegenerative disorder. Mitochondrial dysfunction is believed to contribute to the etiology of PD. Although most cases are sporadic, recent evidence points to a number of genes involved in familial variants of PD. Among them, a loss-of-function of phosphatase and tensin homolog-induced kinase 1 (PINK1; PARK6) is associated with rare cases of autosomal recessive parkinsonism. In HeLa cells, RNA interference-mediated downregulation of PINK1 results in abnormal mitochondrial morphology and altered membrane potential. Morphological changes of mitochondria can be rescued by expression of wild-type PINK1 but not by PD-associated PINK1 mutants. Moreover, primary cells derived from patients with two different PINK1 mutants showed a similar defect in mitochondrial morphology. Human parkin but not PD-associated mutants could rescue mitochondrial pathology in human cells like wild-type PINK1. Our results may therefore suggest that PINK1 deficiency in humans results in mitochondrial abnormalities associated with cellular stress, a pathological phenotype, which can be ameliorated by enhanced expression of parkin.
黑质中多巴胺能神经元的退化是帕金森病(PD)的特征,帕金森病是第二常见的神经退行性疾病。线粒体功能障碍被认为与帕金森病的病因有关。虽然大多数病例是散发性的,但最近的证据表明一些基因与帕金森病的家族性变异有关。其中,磷酸酶和张力蛋白同源物诱导激酶1(PINK1;PARK6)功能丧失与罕见的常染色体隐性帕金森症病例有关。在HeLa细胞中,RNA干扰介导的PINK1下调导致线粒体形态异常和膜电位改变。线粒体的形态变化可以通过野生型PINK1的表达得到挽救,但不能通过与帕金森病相关的PINK1突变体得到挽救。此外,来自具有两种不同PINK1突变体患者的原代细胞在线粒体形态上表现出类似的缺陷。与野生型PINK1一样,人源帕金森蛋白而非与帕金森病相关的突变体可以挽救人细胞中的线粒体病理。因此,我们的结果可能表明,人类中PINK1缺乏会导致与细胞应激相关的线粒体异常,这是一种病理表型,可以通过增强帕金森蛋白的表达来改善。