Liu Peng-Cheng, Liu Kuan, Liu Jun-Feng, Xia Kuo, Chen Li-Yang, Wu Xing
Department of Orthopaedics, Shanghai Tenth People's Hospital, Tongji University, School of Medicine, Shanghai, People's Republic of China.
Department of Rehabilitation, Taihe Hospital, Hubei University of Medicine, Shiyan, Hubei, People's Republic of China.
Oncotarget. 2016 Sep 27;7(39):62873-62885. doi: 10.18632/oncotarget.11871.
The effect of overexpressing the Indian hedgehog (IHH) gene on the chondrogenic differentiation of rabbit bone marrow-derived mesenchymal stem cells (BMSCs) was investigated in a simulated microgravity environment. An adenovirus plasmid encoding the rabbit IHH gene was constructed in vitro and transfected into rabbit BMSCs. Two large groups were used: conventional cell culture and induction model group and simulated microgravity environment group. Each large group was further divided into blank control group, GFP transfection group, and IHH transfection group. During differentiation induction, the expression levels of cartilage-related and cartilage hypertrophy-related genes and proteins in each group were determined. In the conventional model, the IHH transfection group expressed high levels of cartilage-related factors (Coll2 and ANCN) at the early stage of differentiation induction and expressed high levels of cartilage hypertrophy-related factors (Coll10, annexin 5, and ALP) at the late stage. Under the simulated microgravity environment, the IHH transfection group expressed high levels of cartilage-related factors and low levels of cartilage hypertrophy-related factors at all stages of differentiation induction. Under the simulated microgravity environment, transfection of the IHH gene into BMSCs effectively promoted the generation of cartilage and inhibited cartilage aging and osteogenesis. Therefore, this technique is suitable for cartilage tissue engineering.
在模拟微重力环境下,研究了过表达印度刺猬因子(IHH)基因对兔骨髓间充质干细胞(BMSC)软骨分化的影响。体外构建编码兔IHH基因的腺病毒质粒,并将其转染到兔BMSC中。实验分为两大组:常规细胞培养与诱导模型组和模拟微重力环境组。每个大组又进一步分为空白对照组、绿色荧光蛋白(GFP)转染组和IHH转染组。在分化诱导过程中,测定每组中软骨相关基因和蛋白以及软骨肥大相关基因和蛋白的表达水平。在常规模型中,IHH转染组在分化诱导早期表达高水平的软骨相关因子(Ⅱ型胶原(Coll2)和锚蛋白聚糖(ANCN)),在晚期表达高水平的软骨肥大相关因子(Ⅹ型胶原(Coll10)、膜联蛋白5和碱性磷酸酶(ALP))。在模拟微重力环境下,IHH转染组在分化诱导的各个阶段均表达高水平的软骨相关因子和低水平的软骨肥大相关因子。在模拟微重力环境下,将IHH基因转染到BMSC中可有效促进软骨生成并抑制软骨老化和成骨。因此,该技术适用于软骨组织工程。