Wang Zhen, Liang Da-chuan, Bai Jie-yu, Kang Ning, Feng Jun-yu, Yang Zi-quan
Zhongguo Gu Shang. 2015 May;28(5):433-40.
To study the overexpression of Sox9 gene on rabbit bone marrow mesenchymal stem cells for repairing articular cartilage injury in vivo.
Rabbit bone marrow mesenchymal stem cells (BMSCs) were transduced with lentivirus vector containing Sox9 gene and then cartilage specific molecule was detected by RT-PCR in vitro. Total 48 knee joints of 24 mature New Zealand white rabbits were randomly divided into 3 groups according to different defect treatment. After animals anesthesia,a full-thickness cylindrical cartilage defect of 4 mm diameter and 3 mm deep was created in the patellar groove using a stainlesssteel punch. Meanwhile, the transfected cells were implanted to repair the rabbit model with full-thickness cartilage defects. Cartilage defects tissue was observed with light microscope, electron microscope, HE and immunohistochemistry staining to assess the repair of defects by the complex at 6 weeks or 12 weeks after the implantation.
At 3 days after the transfection, Sox9 gene expression was highest and Sox9 gene expression decreased with the increase of time. At 3 days after the transfection, the expression of collagen type II began and reached the peak at 14 days. It showed that the bone marrow mesenchymal stem cells went into chondrogenic differentiation after transfected by Sox9 gene. Histological observation showed that at 6 weeks after the operation, the defects in the experimental group was filled with hyaline like cartilage tissue, 12 weeks after operation,the defects of cartilage and subchondral bone had satisfactory healing. Both at 6 and 12 weeks postoperatively, the defects were filled with fibrous tissues in control groups. Meanwhile, immunohistochemical staining of sections with type II collagen antibodies showed the proteins in the regenerated tissue stained positive for type II collagen and stronger than the control groups. The histological scoring system indicated that the cartilage repair of experiment groups were better than the two control groups with statistical significances.
Overexpression of Sox9 gene on rabbit bone marrow mesenchymal stem cells (BMSCs) promote the repair of cartilage defect.
研究Sox9基因在兔骨髓间充质干细胞中的过表达对体内修复关节软骨损伤的作用。
用携带Sox9基因的慢病毒载体转导兔骨髓间充质干细胞(BMSCs),然后在体外通过RT-PCR检测软骨特异性分子。将24只成年新西兰白兔的48个膝关节根据不同的缺损处理随机分为3组。动物麻醉后,用不锈钢打孔器在髌沟处制作直径4 mm、深3 mm的全层圆柱形软骨缺损。同时,植入转染细胞修复兔全层软骨缺损模型。在植入后6周或12周,用光镜、电镜、HE和免疫组化染色观察软骨缺损组织,评估复合物对缺损的修复情况。
转染后3天,Sox9基因表达最高,且随时间增加Sox9基因表达降低。转染后3天,II型胶原开始表达,并在14天达到峰值。表明骨髓间充质干细胞经Sox9基因转染后进入软骨分化。组织学观察显示,术后6周,实验组缺损处充满透明软骨样组织,术后12周,软骨和软骨下骨缺损愈合良好。术后6周和12周,对照组缺损处均充满纤维组织。同时,用II型胶原抗体对切片进行免疫组化染色,结果显示再生组织中的蛋白II型胶原染色阳性,且强于对照组。组织学评分系统表明,实验组的软骨修复情况优于两个对照组,差异具有统计学意义。
Sox9基因在兔骨髓间充质干细胞(BMSCs)中的过表达促进软骨缺损的修复。