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胶质细胞源性神经营养因子表达脂肪组织源性基质细胞在大鼠帕金森病模型中的植入。

Implantation of glial cell line-derived neurotrophic factor-expressing adipose tissue-derived stromal cells in a rat Parkinson's disease model.

机构信息

Department of Neurosurgery, Huashan Hospital, Fudan University , Shanghai, China.

Department of Nursing, Huashan Hospital North, Fudan University , Shanghai, China.

出版信息

Neurol Res. 2020 Aug;42(8):712-720. doi: 10.1080/01616412.2020.1783473. Epub 2020 Jun 21.

DOI:10.1080/01616412.2020.1783473
PMID:32567526
Abstract

In previous studies, the effects of glial cell line-derived neurotrophic factor (GDNF) expressing adipose tissue-derived stromal cells (ADSCs) on Parkinson's disease (PD) models have been studied but have not been elucidated. The present study aims to investigate this phenomenon and trace their differentiation . In our study, ADSCs were harvested from adult Sprague-Dawley rats, then genetically modified into GDNF-expressing system by lentivirus. The secretion of GDNF from the transduced cells was titrated by enzyme-linked immunosorbent assay (ELISA). Cellular differentiation was observed after induction. To examine survival and differentiation , they were injected into the striatum of 6-hydroxydopamine-lesioned rats, whose apomorphine-induced rotations were examined 2, 7, 14 and 21d after grafting. It's found that GDNF-expressing ADSCs can differentiate into neuron-like cells . Moreover, engrafted GDNF-expressing ADSCs survived at least 90 days post-grafting and differentiated into dopaminergic neuron-like cells. Most importantly, these cells drastically improved the clinical symptoms of PD rats. In conclusion, ADSCs can be efficiently engineered by lentivirus system and deliver a therapeutic level of the transgene to target tissues. GDNF-ADSCs can improve behavior phenotype in the rat PD model. Moreover, ADSCs is a more readily available source of dopaminergic neurons, though a more effective procedure needs to be developed to enrich the number of differentiation.

摘要

在先前的研究中,研究了胶质细胞源性神经营养因子(GDNF)表达脂肪组织来源的基质细胞(ADSCs)对帕金森病(PD)模型的影响,但尚未阐明。本研究旨在研究这一现象并追踪其分化。在我们的研究中,从成年 Sprague-Dawley 大鼠中分离出 ADSCs,然后通过慢病毒将其遗传修饰为 GDNF 表达系统。通过酶联免疫吸附测定(ELISA)测定转导细胞分泌的 GDNF。诱导后观察细胞分化。为了检查生存和分化,将它们注射到 6-羟多巴胺损伤大鼠的纹状体中,在移植后 2、7、14 和 21d 检查阿朴吗啡诱导的旋转。结果发现,GDNF 表达的 ADSCs 可以分化为神经元样细胞。此外,移植的 GDNF 表达的 ADSCs 至少在移植后 90 天内存活并分化为多巴胺能神经元样细胞。最重要的是,这些细胞极大地改善了 PD 大鼠的临床症状。总之,ADSCs 可以通过慢病毒系统有效地进行工程改造,并将治疗水平的转基因递送到靶组织。GDNF-ADSCs 可以改善 PD 大鼠模型的行为表型。此外,ADSCs 是多巴胺能神经元更容易获得的来源,尽管需要开发更有效的程序来增加分化数量。

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