Department of Clinical Neurosciences, University of Cambridge, The Clifford Allbutt Building, Cambridge, CB2 0AH, UK.
School of Neurobiology, Biochemistry and Biophysics, George S. Wise Faculty of Life Sciences, Tel Aviv, Israel.
Acta Neuropathol. 2019 Oct;138(4):575-595. doi: 10.1007/s00401-019-02023-x. Epub 2019 May 31.
Parkinson's disease (PD) is characterized by the presence of α-synuclein aggregates known as Lewy bodies and Lewy neurites, whose formation is linked to disease development. The causal relation between α-synuclein aggregates and PD is not well understood. We generated a new transgenic mouse line (MI2) expressing human, aggregation-prone truncated 1-120 α-synuclein under the control of the tyrosine hydroxylase promoter. MI2 mice exhibit progressive aggregation of α-synuclein in dopaminergic neurons of the substantia nigra pars compacta and their striatal terminals. This is associated with a progressive reduction of striatal dopamine release, reduced striatal innervation and significant nigral dopaminergic nerve cell death starting from 6 and 12 months of age, respectively. In the MI2 mice, alterations in gait impairment can be detected by the DigiGait test from 9 months of age, while gross motor deficit was detected by rotarod test at 20 months of age when 50% of dopaminergic neurons in the substantia nigra pars compacta are lost. These changes were associated with an increase in the number and density of 20-500 nm α-synuclein species as shown by dSTORM. Treatment with the oligomer modulator anle138b, from 9 to 12 months of age, restored striatal dopamine release, prevented dopaminergic cell death and gait impairment. These effects were associated with a reduction of the inner density of large α-synuclein aggregates and an increase in dispersed small α-synuclein species as revealed by dSTORM. The MI2 mouse model recapitulates the progressive dopaminergic deficit observed in PD, showing that early synaptic dysfunction is associated to fine behavioral motor alterations, precedes dopaminergic axonal loss and neuronal death that become associated with a more consistent motor deficit upon reaching a certain threshold. Our data also provide new mechanistic insight for the effect of anle138b's function in vivo supporting that targeting α-synuclein aggregation is a promising therapeutic approach for PD.
帕金森病(PD)的特征是存在被称为路易体和路易神经突的α-突触核蛋白聚集物,其形成与疾病的发展有关。α-突触核蛋白聚集物与 PD 之间的因果关系尚不清楚。我们生成了一种新的转基因小鼠系(MI2),该系在酪氨酸羟化酶启动子的控制下表达人源、易于聚集的截断 1-120α-突触核蛋白。MI2 小鼠表现出多巴胺能神经元中α-突触核蛋白的进行性聚集黑质致密部及其纹状体末端。这与纹状体多巴胺释放的逐渐减少、纹状体神经支配的减少以及从 6 个月和 12 个月龄开始的显著黑质多巴胺能神经元死亡有关。在 MI2 小鼠中,从 9 个月龄开始可以通过 DigiGait 测试检测到步态损伤的改变,而在 20 个月龄时,当黑质致密部 50%的多巴胺能神经元丢失时,通过转棒试验检测到粗大运动缺陷。这些变化与通过 dSTORM 显示的 20-500nmα-突触核蛋白物质的数量和密度增加有关。从 9 到 12 个月龄用寡聚体调节剂 anle138b 治疗,恢复了纹状体多巴胺的释放,防止了多巴胺能细胞死亡和步态损伤。这些作用与通过 dSTORM 揭示的大α-突触核蛋白聚集体的内密度降低和分散的小α-突触核蛋白物质的增加有关。MI2 小鼠模型再现了 PD 中观察到的进行性多巴胺能缺陷,表明早期突触功能障碍与精细运动行为改变有关,在多巴胺能轴突丢失和神经元死亡之前发生,当达到一定阈值时,与更一致的运动缺陷相关。我们的数据还为 anle138b 在体内的作用提供了新的机制见解,支持靶向α-突触核蛋白聚集是治疗 PD 的一种有前途的方法。