T细胞淋巴因子对单核细胞细胞因子基因表达的调控作用。

Lymphokine and cytokine research Pub Date : 1993-12-01
F H Cluitmans, B H Esendam, J E Landegent, R Willemze, J H Falkenburg
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引用次数: 0

摘要

造血是由集落刺激因子(CSF)和许多其他细胞因子调节的。T辅助细胞和单核/巨噬细胞的相互作用发生在免疫反应中,导致许多细胞因子的产生,可能会影响诱导造血。我们研究了辅助性T细胞衍生淋巴因子IL-2、IL-3、GM-CSF和ifn - γ对单核细胞中细胞因子基因表达的影响,并将其与lps诱导的单核细胞中细胞因子基因表达进行了比较。为了避免单核细胞的意外激活,细胞通过洗脱纯化,并在无血清、无lps和非贴壁条件下培养。与LPS类似,IL-2、IL-3和GM-CSF诱导单核细胞IL-1 β、IL-6、IL-8、tnf - α和IL-1- ra基因的表达,但细胞因子mRNA积累的量和动力学存在一定差异。与LPS不同,IL-2、IL-3和GM-CSF不诱导G-CSF和GM-CSF基因在单核细胞中的表达。GM-CSF和IL-3是唯一能够在单核细胞中表达M-CSF基因的诱导剂。IL-2、IL-3和GM-CSF对IL-10基因没有影响,而ifn - γ似乎对单核细胞中研究的任何细胞因子基因都没有影响。这些数据表明,在免疫应答中,促炎细胞因子基因IL-1 β、IL-6、IL-8和tnf - α的表达可以发生,并且IL-1- ra基因的表达等自身调节控制机制也被激活。(摘要删节250字)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Regulatory effects of T cell lymphokines on cytokine gene expression in monocytes.

Hematopoiesis is regulated by colony-stimulating factors (CSF) and many other cytokines. T helper cell and monocyte/macrophage interactions that take place in the immune response, resulting in the production of many cytokines, probably can influence inducible hematopoiesis. We investigated the effect of the T helper cell-derived lymphokines IL-2, IL-3, GM-CSF, and IFN-gamma, on the expression of cytokine genes in monocytes and compared this to LPS-induced cytokine gene expression in monocytes. To avoid inadvertent activation of monocytes, cells were purified by elutriation and cultured under serum-free, LPS-free, and nonadherent conditions. Similar to LPS, IL-2, IL-3, and GM-CSF induced the expression of IL-1 beta, IL-6, IL-8, TNF-alpha, and IL-1-RA genes in monocytes, but with some differences in the amount and kinetics of cytokine mRNA accumulation. Unlike LPS, IL-2, IL-3, and GM-CSF did not induce G-CSF and GM-CSF gene expression in monocytes. GM-CSF and IL-3 were the only inducers capable of expressing the M-CSF gene in monocytes. IL-2, IL-3, and GM-CSF showed no effect on the IL-10 gene while IFN-gamma appeared to have no effect on any of the cytokine genes studied in monocytes. These data indicate that in the immune response expression of the proinflammatory cytokine genes, IL-1 beta, IL-6, IL-8, and TNF-alpha, can occur and that autoregulatory control mechanisms, like the expression of IL-1-RA gene, are also activated.(ABSTRACT TRUNCATED AT 250 WORDS)

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