Cochran F R, Finch-Arietta M B
Department of Allergy and Inflammation, Hoffmann La Roche Inc., Nutley, NJ 07110.
Agents Actions. 1989 Jun;27(3-4):271-3. doi: 10.1007/BF01972794.
Activated macrophages synthesize and release the potent polypeptides, interleukin-1 (IL-1) and tumor necrosis factor (TNF). In an effort to identify the cellular signals which control cytokine production by activated macrophages, we have developed an in vitro model employing the human THP-1 cell line. In the present study, THP-1 cells "primed" by 1.6 microM phorbol 12-myristate-13-acetate (TPA) for 4 hr demonstrated a dose- and time-dependent release of IL-1 beta and TNF upon activation by 20 micrograms/ml LPS. BSA/anti-BSA-coated latex beads were also a potent stimulus for IL-1 beta secretion. Moreover, the combination of a suboptimal concentration of LPS (200 ng/ml) plus interferon-gamma (0.03-333 U/ml) greatly enhanced IL-1 beta production. Resting THP-1 monocytes not "primed" by TPA did not secrete IL-1 beta or TNF. These distinct patterns of cytokine production may be related to the developmental stages of macrophage activation.
活化的巨噬细胞合成并释放强效多肽,白细胞介素-1(IL-1)和肿瘤坏死因子(TNF)。为了确定控制活化巨噬细胞产生细胞因子的细胞信号,我们建立了一种使用人THP-1细胞系的体外模型。在本研究中,经1.6微摩尔佛波醇12-肉豆蔻酸酯-13-乙酸酯(TPA)“预处理”4小时的THP-1细胞,在被20微克/毫升脂多糖(LPS)激活后,呈现出IL-1β和TNF的剂量和时间依赖性释放。牛血清白蛋白/抗牛血清白蛋白包被的乳胶珠也是IL-1β分泌的有效刺激物。此外,次优浓度的LPS(200纳克/毫升)加干扰素-γ(0.03 - 333单位/毫升)的组合极大地增强了IL-1β的产生。未经TPA“预处理”的静息THP-1单核细胞不分泌IL-1β或TNF。这些不同的细胞因子产生模式可能与巨噬细胞活化的发育阶段有关。