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Lentiviral-mediated multiple gene transfer to chondrocytes promotes chondrocyte differentiation and bone formation in rabbit bone marrow-derived mesenchymal stem cells

机译:慢病毒介导的多基因转移到软骨细胞促进兔骨髓间充质干细胞中软骨细胞的分化和骨形成

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The aim of the present study was to provide a theoretical and experimental foundation on the differentiation of stem cells through the induction of multiple genes. The lentiviral vector carrying TGF-beta 1 and IL-10 genes was transfected to bone marrow-derived mesenchymal stem cells (BMSCs) which differentiated into chondrogenesis. Healthy New Zealand white rabbits, 2-3 months of age were used in the present study. A 6-8 ml of bone marrow was isolated from the iliac and tibial shaft of each rabbit. The BMSCs suspension was aspired following centrifugation of the bone marrow by percoll separating medium. The BMSCs were primarily cultured and subcultured in vitro, then divided into four groups according to the difference of lentivirus vectors: group A, receiving transforming growth factor beta 1 (TGF-beta 1); group B, receiving TGF-beta 1 and Interleukin-10 (IL-10); group C, empty vector transfection; and group D, receiving no cell growth factor. Fluorescence expression was detected 12 h after transfecting the lentiviral vector carrying the TGF-beta 1 and IL-10 gene to BMSCs. The transfection efficiency was approximately 70% with a MOI=100 after 96 h. Expression of SOX-9 aggrecan and Type II collagen in groups A-E on day 7 and 14 was detected by RT-PCR and western blot analysis. The expression level of three genes expressed in groups A and C were higher compared to the expression in groups B, D and E. The expression level of the three genes expressed in group B was higher compared to the expression in group D. The expression level of three genes expressed in group A and C showed no statistical difference. Cytokines therefore play an important role in cell proliferation and chondrogenic differentiation. TGF-beta 1 has a synergistic effect in the differentiation. In addition, IL-10 may have a protective role in the restoration of cartilaginous tissue.
机译:本研究的目的是通过诱导多个基因为干细胞的分化提供理论和实验基础。将携带TGF-β1和IL-10基因的慢病毒载体转染到骨髓来源的间充质干细胞(BMSCs)中,该细胞分化为软骨形成。本研究使用了2-3个月大的健康新西兰白兔。从每只兔子的和胫骨干分离出6-8毫升的骨髓。通过percoll分离培养基离心骨髓后,抽吸BMSCs悬液。首先对BMSCs进行体外培养和继代培养,然后根据慢病毒载体的不同将其分为四组:A组,接受转化生长因子β1(TGF-beta 1); B组,接受TGF-beta 1和白介素10(IL-10); C组,空载体转染; D组,没有细胞生长因子。将携带TGF-β1和IL-10基因的慢病毒载体转染到BMSCs后12小时检测到荧光表达。 96小时后MOI = 100时,转染效率约为70%。通过RT-PCR和蛋白质印迹分析检测A-E组在第7天和第14天SOX-9聚集蛋白聚糖和II型胶原的表达。 A和C组表达的三个基因的表达水平高于B,D和E组的表达。B组表达的三个基因的表达水平高于D组的表达。在A和C组中表达的三个基因中的3个显示无统计学差异。因此,细胞因子在细胞增殖和软骨形成分化中起重要作用。 TGF-beta 1在分化中具有协同作用。另外,IL-10在软骨组织的恢复中可能具有保护作用。

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