Tang Yuan, Xiao Jun, Wang Yeyang, Li Ming, Shi Zhanjun
Department of Orthopaedic Surgery, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Department of Orthopaedic Surgery, Third Affiliated Hospital of Southern Medical University, No. 183, Zhongshan West Road, Guangzhou 510631, China.
J Orthop Sci. 2017 Jan;22(1):149-155. doi: 10.1016/j.jos.2016.05.009. Epub 2016 Nov 18.
Articular chondrocytes are important in maintaining normal cartilage tissue and preventing articular degeneration. Exogenous genes have previously been transduced into articular cells using adenoviral vectors to contribute to the maintenance of cell function. This study aimed to transfer the transforming growth factor-β1 gene (TGF-β1) into rabbit articular chondrocytes by adenovirus infection to elucidate its effects on cell function.
Rabbit chondrocytes were isolated and cultured both as monolayers and three-dimensional culture systems. To achieve overexpression, TGF-β1 was transfected by adenovirus infection, using the LacZ gene as a control. TGF-β1 protein expression was analyzed by western blotting. Quantitative DNA fluorometric analysis evaluated cell proliferation, and quantitative reverse transcriptase PCR determined the mRNA expression of related chondrocyte marker genes. Western blotting and glycosaminoglycan quantitative testing were used to examine changes in extracellular matrix components.
TGF-β1 protein expression was found to increase in Adv-TGF-β1-transduced cells, reaching a maximum after chondrocytes had been cultured for 4 weeks. Adv-hTGF-β1 transduction altered chondrocyte morphology from fibrocyte-like long spindle-shaped to round or oval. TGF-β1-transduced cells showed an increase in DNA synthesis, glycosaminoglycan content, and increased aggrecan and collagen II protein expression, while collagen I was significantly decreased. Moreover, TGF-β1 overexpression significantly promoted the mRNA expression of the chondrogenic gene SOX9, and inhibited that of the hypertrophic marker COL10A1 and the mineralization marker MMP-13.
TGF-β1 overexpression positively improved the phenotype, function, and proliferation of chondrocytes, even after several generations.
关节软骨细胞对于维持正常软骨组织及预防关节退变至关重要。此前已使用腺病毒载体将外源基因转导至关节细胞中,以维持细胞功能。本研究旨在通过腺病毒感染将转化生长因子-β1基因(TGF-β1)导入兔关节软骨细胞,以阐明其对细胞功能的影响。
兔软骨细胞通过单层培养和三维培养系统进行分离和培养。为实现过表达,以LacZ基因为对照,通过腺病毒感染转染TGF-β1。通过蛋白质免疫印迹法分析TGF-β1蛋白表达。定量DNA荧光分析评估细胞增殖,定量逆转录聚合酶链反应测定相关软骨细胞标记基因的mRNA表达。采用蛋白质免疫印迹法和糖胺聚糖定量检测来检测细胞外基质成分的变化。
在Adv-TGF-β1转导的细胞中发现TGF-β1蛋白表达增加,在软骨细胞培养4周后达到最大值。Adv-hTGF-β1转导使软骨细胞形态从成纤维细胞样的长梭形变为圆形或椭圆形。TGF-β1转导的细胞显示DNA合成增加、糖胺聚糖含量增加、聚集蛋白聚糖和胶原蛋白II蛋白表达增加,而胶原蛋白I显著减少。此外,TGF-β1过表达显著促进软骨生成基因SOX9的mRNA表达,并抑制肥大标记物COL10A1和矿化标记物MMP-13的表达。
即使经过几代培养,TGF-β1过表达仍能积极改善软骨细胞的表型、功能和增殖。