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Super-CHO—A cell line capable of autocrine growth under fully defined protein-free conditions

机译:Super-CHO-在完全限定的无蛋白条件下能够自分泌生长的细胞系

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Chinese Hamster Ovary (CHO) cells are widely used for the large scale production of recombinant biopharmaceuticals. Growth of the CHO-K1 cell line has been demonstrated in serum-free medium containing insulin, transferrin and selenium. In an attempt to get autocrine growth in protein-free medium, DNA coding for insulin and transferrin production was transfected into CHO-K1 cells. Transferrin was expressed well, with clones secreting approximately 1000 ng/106 cells/24h. Insulin was poorly expressed, with rates peaking at 5 ng/106 cells/24h. Characterisation of the secreted insulin indicated that the CHO cells were incompletely processing the insulin molecule. Site-directed mutagenesis was used to introduce a furin (prohormone converting enzyme) recognition sequence into the insulin molecule, allowing the production of active insulin. However, the levels were still too low to support autocrine growth. Further investigations revealed insulin degrading activity (presumably due to the presence of insulin degrading enzymes) in the cytoplasm of CHO cells. To overcome these problems insulin-like growth factor I (instead of insulin) was transfected into the cells. IGF-1 was completely processed and expressed at rates greater than 500 ng/106cells/24h. In this paper we report autonomous growth of the transfected CHO-K1 cell line expressing transferrin and IGF-1 in protein-free medium without the addition of exogenous growth factors. Growth rates and final cell densities of these cells were identical to that of the parent cell line CHO-K1 growing in insulin, transferrin, and selenium supplemented serum-free media.
机译:中国仓鼠卵巢(CHO)细胞被广泛用于大规模生产重组生物药物。在含有胰岛素,转铁蛋白和硒的无血清培养基中已证明CHO-K1细胞系的生长。为了使自分泌在无蛋白培养基中生长,将编码胰岛素和转铁蛋白生产的DNA转染到CHO-K1细胞中。转铁蛋白表达良好,克隆分泌约1000 ng / 106细胞/ 24h。胰岛素表达不佳,速率峰值为5 ng / 106细胞/ 24h。分泌的胰岛素的表征表明CHO细胞未完全加工胰岛素分子。定点诱变用于将弗林蛋白酶(激素转换酶)识别序列引入胰岛素分子,从而产生活性胰岛素。但是,该水平仍然太低,无法支持自分泌生长。进一步的研究表明,CHO细胞的细胞质中存在胰岛素降解活性(可能是由于胰岛素降解酶的存在)。为了克服这些问题,将胰岛素样生长因子I(而不是胰岛素)转染到细胞中。 IGF-1被完全加工并以大于500 ng / 106cells / 24h的速率表达。在本文中,我们报道了不含蛋白的培养基中不添加外源生长因子的转铁蛋白和IGF-1表达的转染CHO-K1细胞系的自主生长。这些细胞的生长速率和最终细胞密度与在补充胰岛素,转铁蛋白和硒的无血清培养基中生长的亲本细胞系CHO-K1相同。

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