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Organotypic Cultures as a Model of Parkinson´s Disease. A Twist to an Old Model

机译:器官型文化作为帕金森氏病的模型。扭转旧模式

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摘要

Organotypic cultures from the ventral mesencephalon (VM) are widely used to model Parkinson's disease (PD). In this method, neurotoxic compounds have traditionally been applied to the media to induce a uniform dopaminergic (DAergic) cell death in the tissue slices, regardless of the variation existing among slices. This study demonstrates a refinement of the toxic induction technique. We show that unilateral application of 6-hydroxydopamine (6-OHDA) at the tissue surface by means of a microelectrode causes a precisely localized cell death that closely resembles an in vivo stereotactic model. This technique introduces an internal control that accounts for variation between slices and enables a precise quantification of the cell loss due to the toxin in use. We characterized organotypic VM cultures in terms of effects of 6-OHDA toxicity and number of DAergic neurons as judged by immunofluorescence and Western blots. Our findings illustrate that this new application technique greatly improves the representativeness of organotypic cultures as a model for PD.We characterized organotypic VM cultures in terms of effects of 6-OHDA toxicity and number of DAergic neurons as judged by immunofluorescence and Western blots. Our findings illustrate that this new application technique greatly improves the representativeness of organotypic cultures as a model for PD.
机译:腹侧中脑(VM)的器官型培养被广泛用于帕金森氏病(PD)的建模。在这种方法中,传统上已将神经毒性化合物应用于培养基,以诱导组织切片中均匀的多巴胺能(DAergic)细胞死亡,而与切片之间存在的变化无关。这项研究证明了毒性诱导技术的完善。我们表明,通过微电极在组织表面单方面应用6-羟基多巴胺(6-OHDA)导致精确定位的细胞死亡,这非常类似于体内立体定向模型。该技术引入了内部控制,该内部控制解决了切片之间的差异,并能够精确量化由于使用毒素而导致的细胞损失。我们通过免疫荧光和蛋白质印迹判断6-OHDA毒性和DAergic神经元的数量来表征器官型VM培养。我们的发现表明,这种新的应用技术极大地提高了器官型培养物作为PD模型的代表性。我们通过免疫荧光和Western印迹分析了器官型VM培养物对6-OHDA毒性的影响和DA能神经元的数量。我们的发现表明,这种新的应用技术极大地提高了器官型培养物作为PD模型的代表性。

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