Liu Su-Juan, Zou Yu, Belegu Visar, Lv Long-Yun, Lin Na, Wang Ting-Yong, McDonald John W, Zhou Xue, Xia Qing-Jie, Wang Ting-Hua
Department of Histology, Embryology and Neurobiology, West China School of Preclinical and Forensic Medicine, Sichuan University, Chengdu, Sichuan 610041, China.
J Neuroinflammation. 2014 Apr 2;11:66. doi: 10.1186/1742-2094-11-66.
We sought to investigate the effects of co-grafting neural stem cells (NSCs) with olfactory ensheathing cells (OECs) on neurological behavior in rats subjected to traumatic brain injury (TBI) and explore underlying molecular mechanisms.
TBI was established by percussion device made through a weight drop (50 g) from a 30 cm height. Cultured NSCs and OECs isolated from rats were labeled by Hoechst 33342 (blue) and chloromethyl-benzamidodialkyl carbocyanine (CM-Dil) (red), respectively. Then, NSCs and/or OECs, separately or combined, were transplanted into the area surrounding the injury site. Fourteen days after transplantation, neurological severity score (NSS) were recorded. The brain tissue was harvested and processed for immunocytochemistry, terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL), and reverse transcription-polymerase chain reaction (RT-PCR).
Significant neurological function improvement was observed in the three transplant groups, compared to the TBI group, and co-transplantation gave rise to the best improvement. Morphological evaluation showed that the number of neurons in cortex from combination implantation was more than for other groups (P <0.05); conversely, the number of apoptotic cells showed a significant decrease by TUNEL staining. Transplanted NSCs and OECs could survive and migrate in the brain, and the number of neurons differentiating from NSCs in the co-transplantation group was significantly greater than in the NSCs group. At the molecular level, the expressions of IL-6 and BAD in the co-graft group were found to be down regulated significantly, when compared to either the NSC or OEC alone groups.
The present study demonstrates for the first time the optimal effects of co-grafting NSCs and OECs as a new strategy for the treatment of TBI via an anti-inflammation mechanism.
我们试图研究神经干细胞(NSCs)与嗅鞘细胞(OECs)共移植对创伤性脑损伤(TBI)大鼠神经行为的影响,并探索其潜在的分子机制。
通过将50克重物从30厘米高处落下制成的撞击装置建立TBI模型。从大鼠分离培养的NSCs和OECs分别用Hoechst 33342(蓝色)和氯甲基苯甲酰二烷基碳菁(CM-Dil)(红色)标记。然后,将NSCs和/或OECs单独或联合移植到损伤部位周围区域。移植后14天,记录神经严重程度评分(NSS)。收集脑组织进行免疫细胞化学、末端脱氧核苷酸转移酶介导的dUTP缺口末端标记(TUNEL)和逆转录聚合酶链反应(RT-PCR)。
与TBI组相比,三个移植组均观察到明显的神经功能改善,共移植组改善效果最佳。形态学评估显示,联合植入组皮质中的神经元数量多于其他组(P<0.05);相反,TUNEL染色显示凋亡细胞数量显著减少。移植的NSCs和OECs能够在脑内存活并迁移,共移植组中从NSCs分化而来的神经元数量显著多于NSCs组。在分子水平上,与单独的NSC组或OEC组相比,共移植组中IL-6和BAD的表达显著下调。
本研究首次证明了NSCs和OECs共移植作为一种通过抗炎机制治疗TBI的新策略具有最佳效果。