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[肿瘤坏死因子-α在佛波酯和γ干扰素诱导的U937细胞生长与分化中的作用]

[The role of TNF-alpha in the growth and differentiation of U937 cells induced by PMA and IFN-gamma].

作者信息

Wu J, Wang M L, Xu Z, Qiu S L, Zhu J Q, Zhu D X

机构信息

Department of Biochemistry, Nanjing University.

出版信息

Shi Yan Sheng Wu Xue Bao. 1994 Sep;27(3):307-13.

PMID:7801724
Abstract

The effects of PMA and IFN-gamma on regulation of growth and differentiation of human monoblastic leukemic cell U937 were examined. U937 cells were stimulated by different concentrations of PMA and IFN-gamma respectively and NBT reduction assay was used to detect the differentiation of the cells. The results showed that both PMA and IFN-gamma dose-dependently induced differentiation of U937 cells into mature macrophage-like cells. The data also revealed a time-course response in the differentiation induction. Moreover, the U937 cell growth was significantly inhibited by the treatment of PMA and IFN-gamma. These results suggest that PMA and IFN-gamma coupled the regulation of U937 cell growth and differentiation. It was found that tumor necrosis factor-alpha (TNF-alpha) was expressed by the stimulated U937 cells. The specific monoclonal antibody against TNF-alpha diminished the effects of PMA and IFN-gamma on the growth and differentiation of U937 cells. Thus the endogenous TNF-alpha may involved in the mechanism of the effects of PMA and IFN-gamma on the differentiation of U937 cells. The regulatory action of the endogenous TNF-alpha on U937 cells was not due to its cytotoxic effect.

摘要

研究了佛波酯(PMA)和γ干扰素(IFN-γ)对人单核细胞白血病细胞U937生长和分化调控的影响。分别用不同浓度的PMA和IFN-γ刺激U937细胞,采用硝基蓝四氮唑(NBT)还原试验检测细胞分化情况。结果显示,PMA和IFN-γ均呈剂量依赖性地诱导U937细胞分化为成熟的巨噬细胞样细胞。数据还揭示了分化诱导过程中的时间进程反应。此外,PMA和IFN-γ处理显著抑制了U937细胞的生长。这些结果表明,PMA和IFN-γ共同调节U937细胞的生长和分化。发现受刺激的U937细胞表达肿瘤坏死因子-α(TNF-α)。抗TNF-α特异性单克隆抗体减弱了PMA和IFN-γ对U937细胞生长和分化的影响。因此,内源性TNF-α可能参与了PMA和IFN-γ对U937细胞分化作用的机制。内源性TNF-α对U937细胞的调节作用并非由于其细胞毒性作用。

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