Yang Yu-run, Tian Hua
Department of Orthopedics, Third Hospital of Peking University, Beijing 100083, China.
Zhonghua Yi Xue Za Zhi. 2008 Aug 12;88(31):2214-8.
To evaluate the effectiveness of autologous adipose derived mesenchymal stem cells (ADSCs) transduced by adenovirus-mediated human transforming growth factor 2 (Ad-hTGF-beta2) gene in the repair of articular cartilage defects.
Rabbit ADSCs were obtained, cultured, and transfected with Ad-hTGF-beta2 containing human transforming growth factor (hTGF)-beta2. Three days later RT-PCR was used to detect the mRNA expression of hTGF-beta2 in the ADSCs, and ELISA was used to detect the protein expression of hTGF-beta2 in the supernatant. phosphorylation of Smad was examined by Western blotting. Articular cartilage defects at the femoral trochlea were made on 20 rabbits (40 sides) so as to establish animal models. The culture-expanded rabbit ADSCs transfected with Ad-hTGF-2 were seeded on poly (L-lactic-co-glycolic acid) (PLGA) scaffolds. The cell-adhered PLGA scaffolds were implanted into the articular cartilage defects. Plain PLGA was implanted into the left-side defects of 10 rabbits as control group and the defects of 10 sides remained untreated as blank control group. The rabbits were sacrificed 4, 12, and 24 weeks after the operation respectively. The specimens of defects were examined histologically and stained immunohistochemically for type II collagen.
After transfection the ADSCs expressed mRNA and protein expression of hTGF-beta2 and Western blotting showed bands of phosphorylated Smad. The cartilage specimens harvested from the experimental group rabbits demonstrated hyaline cartilage formation mingled closely with the nearby tissues and expression of type II collagen. However, only fibroblasts, not cartilage-like cells, were seen in the control groups that lacked the expression of type II collagen too.
Culture-expanded autologous ADSCs adhered with PLGA composites facilitate the formation of hyaline-cartilage.
评估腺病毒介导的人转化生长因子2(Ad-hTGF-β2)基因转导的自体脂肪间充质干细胞(ADSCs)在修复关节软骨缺损中的有效性。
获取兔ADSCs,进行培养,并用人转化生长因子(hTGF)-β2的Ad-hTGF-β2进行转染。3天后,采用逆转录聚合酶链反应(RT-PCR)检测ADSCs中hTGF-β2的mRNA表达,采用酶联免疫吸附测定(ELISA)检测上清液中hTGF-β2的蛋白表达。通过蛋白质免疫印迹法检测Smad的磷酸化。在20只兔(40侧)的股骨滑车处制造关节软骨缺损,以建立动物模型。将用Ad-hTGF-2转染并经培养扩增的兔ADSCs接种于聚(L-乳酸-共-乙醇酸)(PLGA)支架上。将细胞黏附的PLGA支架植入关节软骨缺损处。将单纯PLGA植入10只兔左侧缺损处作为对照组,10侧缺损处不做处理作为空白对照组。分别在术后4、12和24周处死兔。对缺损标本进行组织学检查,并用免疫组织化学法对Ⅱ型胶原进行染色。
转染后,ADSCs表达hTGF-β2的mRNA和蛋白,蛋白质免疫印迹法显示有磷酸化Smad条带。从实验组兔获取的软骨标本显示有透明软骨形成,与附近组织紧密混合,并表达Ⅱ型胶原。然而,在对照组中仅见成纤维细胞,未见软骨样细胞,且对照组也缺乏Ⅱ型胶原表达。
经培养扩增的自体ADSCs与PLGA复合材料黏附,有利于透明软骨形成。