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Construction of a Recombinant Eukaryotic Expression Plasmid Containing Human Calcitonin Gene and Its Expression in NIH3T3 Cells

机译:降钙素基因重组真核表达质粒的构建及其在NIH3T3细胞中的表达

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Aim. To construct a recombinant eukaryotic expression plasmid containing human calcitonm (hCT) gene and express the gene in murine fibroblast NIH3T3 cells. Materials and Methods. A murine IgK-chain leader sequence and hCT gene were synthesized and cloned into pCDNA3.0 to form the pCDNA3.0-IgK-hCT eukaryotic expression vector, which was transfected into NIH3T3 cells. The mRNA and protein expressions and secretion of hCT were detected. Primarily cultured osteoclasts were incubated with the supernatant of pCDNA3.0-Igk-hCT-transfected NIH3T3 cells, and their numbers were counted and morphology observed. Results. The expression and secretion of hCT were successfully detected in pCDNA3.0-Igk-hCT-transfected NIH3T3 cells. The number of osteoclasts was decreased and the cells became crumpled when they were incubated with the supernatant of pCDNA3.0-Igk-hCT-transfected NIH3T3 cells. Conclusion. A recombinant eukaryotic expression vector containing hCT gene was successfully constructed and expressed in NIH3T3 cells. The secreted recombinant hCT inhibited the growth and morphology of osteoclasts.
机译:目标。构建包含人钙化(hCT)基因的重组真核表达质粒,并在鼠成纤维细胞NIH3T3细胞中表达该基因。材料和方法。合成了鼠IgK链前导序列和hCT基因,并将其克隆到pCDNA3.0中,形成pCDNA3.0-IgK-hCT真核表达载体,将其转染到NIH3T3细胞中。检测hCT的mRNA和蛋白表达以及分泌。将原代培养的破骨细胞与pCDNA3.0-Igk-hCT转染的NIH3T3细胞的上清液一起孵育,计数其数量并观察其形态。结果。在pCDNA3.0-Igk-hCT转染的NIH3T3细胞中成功检测到hCT的表达和分泌。将破骨细胞与pCDNA3.0-Igk-hCT转染的NIH3T3细胞的上清液一起孵育时,破骨细胞的数量减少且细胞皱缩。结论。成功构建了含有hCT基因的重组真核表达载体,并在NIH3T3细胞中表达。分泌的重组hCT抑制破骨细胞的生长和形态。

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