Department of Neurosurgery, Huashan Hospital, Fudan University , Shanghai, China.
Department of Nursing, Huashan Hospital North, Fudan University , Shanghai, China.
Neurol Res. 2020 Aug;42(8):712-720. doi: 10.1080/01616412.2020.1783473. Epub 2020 Jun 21.
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.
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。