Division of Stem Cell Research, Department of Biomedical Research and Innovation, Institute for Clinical Research, National Hospital Organization Osaka National Hospital, Japan.
Department of Neurology, Graduate School of Medicine, Osaka University, Japan.
FEBS Open Bio. 2021 Feb;11(2):354-366. doi: 10.1002/2211-5463.13060. Epub 2021 Jan 5.
Parkinson's disease (PD) is a neurodegenerative disorder caused by the selective loss of dopaminergic (DA) neurons in the substantia nigra pars compacta (SNc). Lewy bodies (LBs), another histological hallmark of PD, are observed in patients with familial or sporadic PD. The therapeutic potential of reducing the accumulation of α-synuclein, a major LB component, has been investigated, but it remains unknown whether the formation of LBs results in the loss of DA neurons. PARK4 patients exhibit multiplication of the α-synuclein gene (SNCA) without any pathological mutations, but their symptoms develop relatively early. Therefore, study of PARK4 might help elucidate the mechanism of α-synuclein aggregation. In this study, we investigated the dynamics of α-synuclein during the early stage of immature DA neurons, which were differentiated from human-induced pluripotent stem cells (hiPSCs) derived from either a PARK4 patient with SNCA triplication or a healthy donor. We observed increased α-synuclein accumulation in PARK4 hiPSC-derived DA neurons relative to those derived from healthy donor hiPSCs. Interestingly, α-synuclein accumulation disappeared over time in the PARK4 patient-derived DA neurons. Moreover, an SNCA-specific antisense oligonucleotide could reduce α-synuclein levels during the accumulation stage. These observations may help reveal the mechanisms that regulate α-synuclein levels, which may consequently be useful in the development of new therapies for patients with sporadic or familial PD.
帕金森病(PD)是一种神经退行性疾病,由黑质致密部(SNc)中的多巴胺能(DA)神经元选择性丧失引起。路易体(LB)是 PD 的另一个组织学标志,在家族性或散发性 PD 患者中观察到。减少α-突触核蛋白(一种主要的 LB 成分)积累的治疗潜力已经得到了研究,但尚不清楚 LB 的形成是否导致 DA 神经元的丧失。PARK4 患者表现出α-突触核蛋白基因(SNCA)的倍增,而没有任何病理突变,但他们的症状相对较早出现。因此,对 PARK4 的研究可能有助于阐明α-突触核蛋白聚集的机制。在这项研究中,我们研究了来自 PARK4 患者或健康供体的诱导多能干细胞(hiPSC)分化而来的未成熟 DA 神经元早期阶段α-突触核蛋白的动态变化。与来自健康供体 hiPSC 的 DA 神经元相比,PARK4 hiPSC 衍生的 DA 神经元中α-突触核蛋白的积累增加。有趣的是,PARK4 患者来源的 DA 神经元中α-突触核蛋白的积累随时间消失。此外,一种针对 SNCA 的特异性反义寡核苷酸可以在积累阶段降低α-突触核蛋白水平。这些观察结果可能有助于揭示调节α-突触核蛋白水平的机制,这可能有助于开发针对散发性或家族性 PD 患者的新疗法。