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人白血病髓细胞的“分化诱导”培养刺激巨噬细胞分化诱导因子的高产量。

"Differentiation induction" culture of human leukemic myeloid cells stimulates high production of macrophage differentiation inducing factor.

作者信息

Abe T, Ohno M, Sato T, Murakami M, Kajiki M, Kodaira R

机构信息

Life Science Laboratories, Ashi Chemical Industry Co., Ltd., Shizuoka, Japan.

出版信息

Cytotechnology. 1991;5 Suppl 2:S75-93.

PMID:1367527
Abstract

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 a Mycoplasma 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-alpha (TNF-alpha), interleukin-1 alpha (IL-1 alpha) and interleukin-1 beta (IL-1 beta), 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 micrograms/10(6) 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.

摘要

一种适合生产人单核因子的方法被定义为“分化诱导”培养。通过用大戟二萜醇、视黄酸和发酵支原体提取物的组合诱导,人单核细胞白血病THP - 1细胞从无功能的前单核细胞充分分化为巨噬细胞样细胞。分化后的THP - 1细胞分泌大量巨噬细胞分化诱导因子(DIF)活性,并同时向培养基中产生其他已知的单核因子,如肿瘤坏死因子-α(TNF-α)、白细胞介素-1α(IL-1α)和白细胞介素-1β(IL-1β)。这些结果表明,在本研究定义的“分化诱导”培养条件诱导的THP - 1细胞的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被纯化至同质,氨基末端氨基酸序列分析表明巨噬细胞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,并从用LIF cDNA转染的中国仓鼠卵巢(CHO)细胞中筛选出产生3.7微克/10⁶细胞·天重组LIF的克隆。使用M1细胞的MTT还原测定法定量CHO细胞中的重组LIF产量。

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