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淋巴细胞对完全成熟巨噬细胞产生粒单系造血增强因子的影响。

Effect of lymphocytes on the production of granulomonopoietic enhancing factor by fully mature macrophages.

作者信息

Wang S Y, Chen L Y, Hsu M L, Tzeng C H, Ho C H, Ho C K

机构信息

Department of Medical Research, Veterans General Hospital-Taipei, Taiwan, Republic of China.

出版信息

Stem Cells. 1995 Jul;13(4):435-44. doi: 10.1002/stem.5530130415.

Abstract

The granulomonopoietic enhancing factor (GM-EF) is a novel myelopoietic regulator produced by human monocyte-derived lipid-containing macrophages (MDLMs). In the present study, we examined the effect of lymphocytes on GM-EF production by preincubation of MDLMs with various preparations of lymphocyte subpopulations in cell-mixed and in double agar layer cultures. Our results showed that a cell concentration-dependent suppression of GM-EF production was noted in cultures with mitogen-activated T cells, and mitogen-activated/resting B cells, while those containing resting T cells had no such effect. Thus, GM-EF production in the presence of 1 x 10(5)/ml activated T cells or activated/resting B cells was greatly reduced to 5% or 20%, respectively. The lymphocyte-induced suppression was evident in both cell-mixed and double layer cultures, implying that the effector cells might exert their influences via mediators. Assay for cytokine activity revealed that a high level (648.2-685.2 pg/ml) of tumor necrosis factor-alpha (TNF-alpha) was found in MDLM cultures with resting/activated B cells, and in those with activated T cells high levels of both TNF-alpha (510.5 pg/ml) and interferon-gamma (IFN-gamma) (321.3 pg/ml) could be detected, whereas in cultures with MDLMs and/or resting T cells, these cytokines were not measurable. Treatment of MDLMs with either recombinant (r) TNF-alpha or rIFN-gamma invariably resulted in a dose-dependent decrease in GM-EF production with intense suppression at doses between 400-800 U/ml.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

粒单系造血增强因子(GM-EF)是一种由人单核细胞衍生的含脂质巨噬细胞(MDLM)产生的新型骨髓造血调节因子。在本研究中,我们通过在细胞混合培养和双层琼脂培养中,将MDLM与各种淋巴细胞亚群制剂预孵育,来检测淋巴细胞对GM-EF产生的影响。我们的结果显示,在有丝分裂原激活的T细胞以及有丝分裂原激活/静止B细胞的培养物中,观察到GM-EF产生呈细胞浓度依赖性抑制,而含有静止T细胞的培养物则无此效应。因此,在存在1×10⁵/ml激活T细胞或激活/静止B细胞的情况下,GM-EF的产生分别大幅降低至5%或20%。淋巴细胞诱导的抑制在细胞混合培养和双层培养中均很明显,这意味着效应细胞可能通过介质发挥作用。细胞因子活性检测显示,在含有静止/激活B细胞的MDLM培养物中发现高水平(648.2 - 685.2 pg/ml)的肿瘤坏死因子-α(TNF-α),在含有激活T细胞的培养物中可检测到高水平的TNF-α(510.5 pg/ml)和干扰素-γ(IFN-γ)(321.3 pg/ml),而在含有MDLM和/或静止T细胞的培养物中,这些细胞因子无法检测到。用重组(r)TNF-α或rIFN-γ处理MDLM总是导致GM-EF产生呈剂量依赖性下降,在400 - 800 U/ml剂量时抑制强烈。(摘要截断于250字)

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