Inserm, U 1127, F-75013 Paris, France; CNRS, UMR 7225, F-75013 Paris, France; Sorbonne Universités, UPMC Univ Paris 06, UMRS 1127, F-75013 Paris, France; Institut du Cerveau et de la Moelle Epinière, ICM, F-75013 Paris, France.
Inserm, U 1127, F-75013 Paris, France; CNRS, UMR 7225, F-75013 Paris, France; Sorbonne Universités, UPMC Univ Paris 06, UMRS 1127, F-75013 Paris, France; Institut du Cerveau et de la Moelle Epinière, ICM, F-75013 Paris, France.
Neuron. 2016 May 18;90(4):675-91. doi: 10.1016/j.neuron.2016.03.038.
Parkinson disease (PD) is a multifactorial neurodegenerative disorder, the etiology of which remains largely unknown. Progressive impairment of voluntary motor control, which represents the primary clinical feature of the disease, is caused by a loss of midbrain substantia nigra dopamine (DA) neurons. We present here a synthetic overview of cell-autonomous mechanisms that are likely to participate in DA cell death in both sporadic and inherited forms of the disease. In particular, we describe how damage to vulnerable DA neurons may arise from cellular disturbances produced by protein misfolding and aggregation, disruption of autophagic catabolism, endoplasmic reticulum (ER) stress, mitochondrial dysfunction, or loss of calcium homeostasis. Where pertinent, we show how these mechanisms may mutually cooperate to promote neuronal death.
帕金森病(PD)是一种多因素神经退行性疾病,其病因在很大程度上仍然未知。中脑黑质多巴胺(DA)神经元的逐渐丧失导致了运动控制的逐渐受损,这是该疾病的主要临床特征。我们在这里综合介绍了可能参与散发性和遗传性疾病中 DA 细胞死亡的细胞自主机制。特别是,我们描述了脆弱的 DA 神经元的损伤如何可能是由蛋白质错误折叠和聚集、自噬分解代谢中断、内质网(ER)应激、线粒体功能障碍或钙稳态丧失引起的细胞紊乱导致的。在相关情况下,我们展示了这些机制如何相互合作以促进神经元死亡。