LUNAM University, Angers University, France; INSERM UMR S_1066, Angers University, France.
LUNAM University, Angers University, France; INSERM UMR S_1066, Angers University, France; Pharmacy and Pharmaceutical Technology Department, University of Navarra, Pamplona, Spain.
Neuroscience. 2014 Jan 3;256:10-22. doi: 10.1016/j.neuroscience.2013.10.021. Epub 2013 Oct 23.
Parkinson's disease (PD) is the second most frequent neurodegenerative disorder afflicting 2% of the population older than 65 years worldwide. Recently, brain organotypic slices have been used to model neurodegenerative disorders, including PD. They conserve brain three-dimensional architecture, synaptic connectivity and its microenvironment. This model has allowed researchers a simple and rapid method to observe cellular interactions and mechanisms. In the present study, we developed an organotypic PD model from rat brains that includes all the areas involved in the nigrostriatal pathway in a single slice preparation, without using neurotoxins to induce the dopaminergic lesion. The mechanical transection of the nigrostriatal pathway obtained during slice preparation induced PD-like histopathology. Progressive nigrostriatal degeneration was monitored combining innovative approaches, such as diffusion tensor magnetic resonance imaging (DT-RMI) to follow fiber degeneration and mass spectrometry to quantify striatal dopamine content, together with bright-field and fluorescence microscopy imaging. A substantia nigra dopaminergic cell number decrease was observed by immunohistochemistry against rat tyrosine hydroxylase (TH) reaching 80% after 2 days in culture associated with a 30% decrease of striatal TH-positive fiber density, a 15% loss of striatal dopamine content quantified by mass spectrometry and a 70% reduction of nigrostriatal fiber fractional anisotropy quantified by DT-RMI. In addition, a significant decline of medium spiny neuron density was observed from days 7 to 16. These sagittal organotypic slices could be used to study the early stage of PD, namely dopaminergic degeneration, and the late stage of the pathology with dopaminergic and GABAergic neuron loss. This novel model might improve the understanding of PD and may represent a promising tool to refine the evaluation of new therapeutic approaches.
帕金森病(PD)是全球 65 岁以上人群中第二常见的神经退行性疾病,发病率为 2%。最近,脑器官型切片已被用于模拟神经退行性疾病,包括 PD。它们保留了脑的三维结构、突触连接及其微环境。这种模型使研究人员能够简单快速地观察细胞相互作用和机制。在本研究中,我们从大鼠脑中开发了一种器官型 PD 模型,该模型在单个切片制备中包含了参与黑质纹状体通路的所有区域,而无需使用神经毒素来诱导多巴胺能损伤。切片制备过程中对黑质纹状体通路的机械横断导致了 PD 样组织病理学改变。通过结合创新方法(如扩散张量磁共振成像(DT-RMI)来跟踪纤维变性和质谱法来定量纹状体多巴胺含量),同时结合明场和荧光显微镜成像,监测进行性黑质纹状体变性。通过针对大鼠酪氨酸羟化酶(TH)的免疫组织化学观察到黑质多巴胺能细胞数量减少,培养 2 天后减少了 80%,同时纹状体 TH 阳性纤维密度降低了 30%,通过质谱法定量的纹状体多巴胺含量降低了 15%,通过 DT-RMI 定量的黑质纹状体纤维各向异性分数降低了 70%。此外,从第 7 天到第 16 天观察到中间多棘神经元密度显著下降。这些矢状器官型切片可用于研究 PD 的早期阶段,即多巴胺能变性,以及后期的多巴胺能和 GABA 能神经元丧失的阶段。这种新模型可能有助于更好地理解 PD,并可能成为评估新治疗方法的有前途的工具。