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Derivation of Leptomeninges Explant Cultures from Postmortem Human Brain Donors

机译:死后人类脑供体的轻薄肉外植体培养物的衍生

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摘要

Even though great progress has been made in the clinical characterization of Parkinson's disease, several studies report that the diagnosis of Parkinson's disease is not pathologically confirmed in up to 25% of clinically diagnosed Parkinson's disease. Therefore, tissue collected from clinically diagnosed patients with idiopathic Parkinson's disease can have a high rate of misdiagnosis; hence in vitro studies from such tissues to study Parkinson's disease as a preclinical model can become futile.By collecting postmortem human leptomeninges with a confirmed neuropathological diagnosis of Parkinson's disease and characterized by nigrostriatal cell loss and intracellular protein inclusions called Lewy bodies, one can be certain that clinically observed parkinsonism is not caused by another underlying disease process (e.g. tumor, arteriosclerosis).This protocol presents the dissection and preparation of postmortem human leptomeninges for derivation of a meningeal fibroblast culture. This procedure is robust and has a high success rate. The challenge of the culture is sterility as the brain procurement is generally not performed under sterile conditions. Therefore, it is important to supplement the culture media with a cocktail of penicillin, streptomycin, and amphotericin B.The derivation of meningeal fibroblasts from autopsy-confirmed cases with Parkinson's disease provides the foundation for in vitro modeling of Parkinson's disease. Meningeal fibroblasts appear 3-9 days after sample preparation and about 20-30 million cells can be cryopreserved in 6-8 weeks. The meningeal fibroblast culture is homogenous and the cells express fibronectin, a commonly used marker to identify meninges.
机译:尽管在帕金森氏病的临床表征方面已经取得了很大的进步,但一些研究报告指出,在高达25%的临床诊断出的帕金森氏病中,尚无病理证实帕金森氏病的诊断。因此,从临床诊断为特发性帕金森氏病的患者中收集的组织可能有很高的误诊率;因此,从这样的组织进行体外研究以将帕金森氏病作为临床前模型可能会徒劳无功。通过收集死后的人类软脑膜小球,以确诊为帕金森氏病的神经病理学诊断为特征,其特征是黑质纹状体细胞丢失和称为路易小体的细胞内蛋白质包涵体临床观察到的帕金森氏症不是由另一种潜在的疾病过程(例如肿瘤,动脉硬化)引起的。本方案介绍了解剖和制备人脑软脑膜后脑膜成纤维细胞培养物的制备方法。该过程是鲁棒的,并且具有很高的成功率。培养的挑战是无菌,因为大脑采购通常不在无菌条件下进行。因此,重要的是在培养基中添加青霉素,链霉素和两性霉素B的混合物。从帕金森氏病经尸检确认的病例中提取脑膜成纤维细胞为帕金森氏病的体外建模提供了基础。脑膜成纤维细胞在样品制备后3-9天出现,大约20-30,000,000个细胞可以在6-8周内冷冻保存。脑膜成纤维细胞培养物是均质的,细胞表达纤连蛋白,这是鉴定脑膜的常用标记。

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