Laboratory of Neurodegenerative Diseases, Institute of Health Sciences, Shanghai Institutes for Biological Sciences, Chinese Academy of Science and Shanghai Jiaotong University School of Medicine, Shanghai, PR China.
Neurobiol Aging. 2013 Feb;34(2):489-98. doi: 10.1016/j.neurobiolaging.2012.04.008. Epub 2012 May 19.
Parkinson's disease (PD) is a common neurodegenerative disease characterized by the selective loss of the dopaminergic (DA) neurons in substantia nigra. The degeneration leads to decreased levels of DA in striatum and causes uncontrolled firing of innervated medium spiny neurons (MSNs), thus preventing the patient to act smoothly. Gene-specific deficient mouse models for the recessive forms of PD were generated in the past decade, although most failed to exhibit degeneration of DA neurons or decreased DA level, as evidenced in PD patients. Here by using DJ-1-knockdown neuroblastoma SH-SY5Y cells and Neuro-2a cells as well as DJ-1-deficient mice, we found DJ-1 deficiency could downregulate β-tubulin III via a hypoxia-inducible factor 1α (HIF-1α) pathway, and, correspondingly, we observed reduced microtubule dynamics. With Golgi-Cox impregnation, we also observed declined dendritic complexity and the loss of dendritic spines in striatal MSNs of DJ-1-deficient mice. Our results revealed a novel role of DJ-1 in the regulation of microtubule dynamics and suggested that striatal impairments may also play an important role as loss of DA neurons in the pathogenesis of PD.
帕金森病(PD)是一种常见的神经退行性疾病,其特征是黑质中多巴胺能(DA)神经元的选择性丧失。退化导致纹状体中 DA 水平降低,并导致支配的中型多棘神经元(MSNs)不受控制地放电,从而阻止患者顺利行动。过去十年中,已经生成了用于 PD 隐性形式的基因特异性缺陷型小鼠模型,尽管大多数模型未能表现出 DA 神经元的退化或 DA 水平的降低,如 PD 患者中所见。在这里,我们使用 DJ-1 敲低的神经母细胞瘤 SH-SY5Y 细胞和 Neuro-2a 细胞以及 DJ-1 缺陷型小鼠,发现 DJ-1 缺乏可通过缺氧诱导因子 1α(HIF-1α)途径下调 β-微管蛋白 III,并且相应地,我们观察到微管动力学降低。通过高尔基-Cox 浸渍,我们还观察到 DJ-1 缺陷型小鼠纹状体 MSNs 中树突复杂性降低和树突棘丢失。我们的结果揭示了 DJ-1 在微管动力学调节中的新作用,并表明纹状体损伤也可能在 PD 的发病机制中与 DA 神经元丧失一样发挥重要作用。