首页> 外文期刊>Osteoarthritis and cartilage >Electroporation-mediated gene transfer of SOX trio to enhance chondrogenesis in adipose stem cells.
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Electroporation-mediated gene transfer of SOX trio to enhance chondrogenesis in adipose stem cells.

机译:SOX trio的电穿孔介导的基因转移可增强脂肪干细胞的软骨形成。

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OBJECTIVE: The aim of the present study was to determine if the electroporation-mediated gene transfer of SOX trio enhances the chondrogenic potential of adipose stem cells (ASCs). DESIGN: ASCs were transfected with SOX trio genes using an electroporation technique and cultured for 3 weeks. The pellets were analyzed for DNA and glycosaminoglycan (GAG) analysis, and the gene and protein expression of SOX-5, SOX-6, SOX-9, type 1 collagen (COL1Al), type 2 collagen (COL2Al) and type 10 collagen (COL10A1) using real-time PCR and Western blot analysis. Further in vivo studies were carried out by subcutaneous transplantation of pellets in severe combined immunodeficiency (SCID) mice for 3 weeks. RESULTS: The gene transfer efficiency was high (approximately 70%). Transfected ASCs showed high expression of corresponding genes after 21 days, and each SOX protein was detected in ASCs transfected with the corresponding gene. The chondrogenic differentiation of ASCs, as demonstrated by GAG levels and Safranin-O staining, showed significant enhancement when SOX trio were co-transfected, while subsets with single gene transfer of SOX-5, -6, or -9 did not show significant elevation. SOX trio co-transfection enhanced COL2A1 mRNA, but did not increase COL1A1 and COL10A1 mRNA. Type II collagen protein dramatically increased, and type X collagen decreased with co-transfection of the SOX trio. When pellets were implanted in the subcutaneous pouch of SCID mice for 3 weeks, ASCs co-transfected with SOX trio demonstrated abundant proteoglycan, significantly reduced mineralization. CONCLUSION: The electroporation-mediated transfection of SOX trio greatly enhances chondrogenesis from ASCs, while decreasing hypertrophy.
机译:目的:本研究的目的是确定电穿孔介导的SOX trio基因转移是否增强了脂肪干细胞(ASCs)的软骨形成潜能。设计:使用电穿孔技术将SOX trio基因转染ASC,并培养3周。分析沉淀物的DNA和糖胺聚糖(GAG)分析,以及SOX-5,SOX-6,SOX-9、1型胶原(COL1A1),2型胶原(COL2A1)和10型胶原( COL10A1)使用实时PCR和Western blot分析。通过在严重的联合免疫缺陷(SCID)小鼠中皮下移植颗粒3周,进行了进一步的体内研究。结果:基因转移效率高(约70%)。转染的ASC在21天后显示出相应基因的高表达,并且在用相应基因转染的ASC中检测到每种SOX蛋白。 GAG水平和Safranin-O染色表明,ASC的软骨形成分化在共转染SOX三重奏时显示出显着增强,而具有SOX-5,-6或-9的单基因转移的子集则没有显着升高。 SOX trio共转染可增强COL2A1 mRNA,但不会增加COL1A1和COL10A1 mRNA。随着SOX三重奏的共转染,II型胶原蛋白蛋白质急剧增加,而X型胶原蛋白减少。将小球植入SCID小鼠的皮下袋中3周后,与SOX trio共转染的ASCs表现出丰富的蛋白聚糖,显着减少了矿化作用。结论:电穿孔介导的SOX trio转染大大增强了ASC的软骨形成,同时减少了肥大。

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