Tang Linjun, Lu Xiaocheng, Zhu Ronglan, Qian Tengda, Tao Yi, Li Kai, Zheng Jinyu, Zhao Penglai, Li Shuai, Wang Xi, Li Lixin
Department of Neurosurgery, The First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, Nanjing, 210029, Jiangsu, China.
Department of Neurosurgery, Tongling Municipal Hospital, Tongling, 244000, Anhui, China.
Cell Mol Neurobiol. 2016 Jul;36(5):657-67. doi: 10.1007/s10571-015-0246-y. Epub 2015 Aug 18.
Neurogenin2 (Ngn2) is a proneural gene that directs neuronal differentiation of progenitor cells during development. This study aimed to investigate whether the use of adipose-derived stem cells (ADSCs) over-expressing the Ngn2 transgene (Ngn2-ADSCs) could display the characteristics of neurogenic cells and improve functional recovery in an experimental rat model of SCI. ADSCs from rats were cultured and purified in vitro, followed by genetically modified with the Ngn2 gene. Forty-eight adult female Sprague-Dawley rats were randomly assigned to three groups: the control, ADSCs, and Ngn2-ADSCs groups. The hind-limb motor function of all rats was recorded using the Basso, Beattie, and Bresnahan locomotor rating scale for 8 weeks. Moreover, hematoxylineosin staining and immunohistochemistry were also performed. After neural induction, positive expression rate of NeuN in Ngn2-ADSCs group was upon 90 %. Following transplantation, a great number of ADSCs was found around the center of the injury spinal cord at 1 and 4 weeks, which improved retention of tissue at the lesion site. Ngn2-ADSCs differentiated into neurons, indicated by the expression of neuronal markers, NeuN and Tuj1. Additionally, transplantation of Ngn2-ADSCs upregulated the trophic factors (brain-derived neurotrophic factor and vascular endothelial growth factor), and inhibited the glial scar formation, which was indicated by immunohistochemistry with glial fibrillary acidic protein. Finally, Ngn2-ADSCs-treated animals showed the highest functional recovery among the three groups. These findings suggest that transplantation of Ngn2-overexpressed ADSCs promote the functional recovery from SCI, and improve the local microenvironment of injured cord in a more efficient way than that with ADSCs alone.
神经生成素2(Ngn2)是一种原神经基因,在发育过程中指导祖细胞的神经元分化。本研究旨在探讨使用过表达Ngn2转基因的脂肪来源干细胞(ADSCs,即Ngn2 - ADSCs)是否能在脊髓损伤(SCI)实验大鼠模型中表现出神经源性细胞的特征并改善功能恢复。从大鼠中分离出ADSCs并在体外进行培养和纯化,随后用Ngn2基因进行基因改造。48只成年雌性Sprague - Dawley大鼠被随机分为三组:对照组、ADSCs组和Ngn2 - ADSCs组。使用Basso、Beattie和Bresnahan运动评分量表记录所有大鼠的后肢运动功能,为期8周。此外,还进行了苏木精 - 伊红染色和免疫组织化学检测。神经诱导后,Ngn2 - ADSCs组中NeuN的阳性表达率超过90%。移植后,在1周和4周时发现损伤脊髓中心周围有大量ADSCs,这改善了损伤部位的组织保留情况。Ngn2 - ADSCs分化为神经元,神经元标志物NeuN和Tuj1的表达表明了这一点。此外,Ngn2 - ADSCs的移植上调了营养因子(脑源性神经营养因子和血管内皮生长因子),并抑制了胶质瘢痕形成,这通过胶质纤维酸性蛋白免疫组织化学得以证实。最后,在三组中,接受Ngn2 - ADSCs治疗的动物功能恢复最佳。这些发现表明,移植过表达Ngn2的ADSCs可促进SCI后的功能恢复,并比单独使用ADSCs更有效地改善损伤脊髓的局部微环境。