Wang Ting-Hua, Feng Zhong-Tang, Wei Peng, Li Hui, Shi Zhen-Jiang, Li Li-Yan
Department of Histology, Embryology and Neurobiology, West China School of Preclinical and Forensic Medicine, Sichuan University, Chengdu, 610041, China.
J Mol Neurosci. 2008 Jun;35(2):161-9. doi: 10.1007/s12031-007-9032-8. Epub 2008 Feb 14.
This study determined the effects of pcDNA3-beta-nerve growth factor (NGF) gene-modified bone marrow stromal cells (BMSC) on the rat model of Parkinson's disease (PD). The recombinant plasmid pcDNA3-beta-NGF was transfected into BMSC, and NGF expression and its biological activity in vitro were detected. BMSC modified by the NGF gene were then grafted into the corpus striatum of PD rats, and the rotation behavior was evaluated at 1, 2, 4, and 6 weeks post-transplantation. A significant improvement in rotation behavior was observed in PD rats subjected to cell transplantation, especially in PD rats receiving NGF-modified BMSC. The genetically modified BMSC survived and expressed beta-NGF but did not differentiate into tyrosine hydroxylase-positive cells in vivo. The present findings suggested that genetically modified BMSC could be effective for PD treatment, and the mechanisms might involve the neuroprotective effects of beta-NGF.
本研究确定了pcDNA3-β-神经生长因子(NGF)基因修饰的骨髓基质细胞(BMSC)对帕金森病(PD)大鼠模型的影响。将重组质粒pcDNA3-β-NGF转染到BMSC中,并检测其体外NGF表达及其生物学活性。然后将经NGF基因修饰的BMSC移植到PD大鼠的纹状体中,并在移植后1、2、4和6周评估旋转行为。在接受细胞移植的PD大鼠中观察到旋转行为有显著改善,尤其是在接受NGF修饰的BMSC的PD大鼠中。基因修饰的BMSC在体内存活并表达β-NGF,但未分化为酪氨酸羟化酶阳性细胞。目前的研究结果表明,基因修饰的BMSC可能对PD治疗有效,其机制可能涉及β-NGF的神经保护作用。