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首页> 外文期刊>Cytotechnology >“Differentiation Induction” culture of human leukemic myeloid cells stimulates high production of macrophage differentiation inducing factor
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“Differentiation Induction” culture of human leukemic myeloid cells stimulates high production of macrophage differentiation inducing factor

机译:人白血病髓样细胞的“分化诱导”培养可刺激巨噬细胞分化诱导因子的大量产生

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摘要

A suitable procedure for the production of human monokines was defined as ‘differentiation-induction’ culture. Human monocytic leukemia THP-1 cells were well-differentiated from nonfunctional promonocytes into macrophage-like cells by the induction with a combination of mezerein, retinoic acid, and aMycoplasma fermentans extract. The differentiated THP-1 cells secreted a high amount of macrophage differentiation-inducing factor (DIF) activity and concomitantly produced other known monokines, such as tumor necrosis factor-α (TNF-α), interleukin-1α (IL-1α) and interleukin-1β (IL-1β), into the medium. These results suggest that other novel human monokines may also be found in the conditioned medium of THP-1 cells induced by the ‘differentiation-induction’ culture conditions defined in this study. Macrophage DIF was purified to homogeneity and NH2-terminal amino acid sequence analysis revealed that macrophage DIF is very similar or identical to human leukemia inhibitory factor (LIF). The cDNA encoding human LIF was isolated using the polymerase chain reaction, and a clone producing 3.7 μg/106 cells day recombinant LIF was selected from Chinese hamster ovary (CHO) cells which were transfected with the LIF cDNA. The recombinant LIF production in CHO cells was quantified using MTT reduction assay with M1 cells.
机译:一种合适的生产人类单核因子的程序被定义为“分化诱导”文化。通过结合美ze素,视黄酸和发酵支原体提取物诱导,人单核细胞白血病THP-1细胞从非功能性原代细胞分化为巨噬细胞样细胞。分化的THP-1细胞分泌大量巨噬细胞分化诱导因子(DIF)活性,并同时产生其他已知的单核因子,例如肿瘤坏死因子-α(TNF-α),白介素-1α(IL-1α)和白介素-1β(IL-1β),进入培养基。这些结果表明,在本研究中定义的“分化诱导”培养条件诱导的THP-1细胞条件培养基中也可能发现其他新型人单核因子。巨噬细胞DIF被纯化至均一,并且NH 2末端氨基酸序列分析显示巨噬细胞DIF与人白血病抑制因子(LIF)非常相似或相同。使用聚合酶链反应分离编码人LIF的cDNA,并从转染了LIF cDNA的中国仓鼠卵巢(CHO)细胞中选择一个产生3.7μg/ 106细胞日重组LIF的克隆。使用M1细胞的MTT还原法对CHO细胞中重组LIF的产生进行定量。

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