Sugama K, Kuwano K, Furukawa M, Himeno Y, Satoh T, Arai S
Department of Microbiology, Kurume University School of Medicine, Japan.
Infect Immun. 1990 Nov;58(11):3564-7. doi: 10.1128/iai.58.11.3564-3567.1990.
We demonstrated that mycoplasmas (MP), previously shown to augment the antitumor activity of murine peritoneal macrophages, also induce cytotoxic activity in a human monocytic cell line, THP-1. THP-1 cells were induced to produce cytotoxic activity by MP in a time- and dose-dependent manner. By using neutralization by antibody against tumor necrosis factor (TNF), the cytotoxic activity was shown to be due to TNF released from the MP-stimulated cells. Studies with inhibitors of second-messenger pathways and Northern RNA blot analysis indicated that a Ca2(+)-dependent, but not protein kinase C-dependent, biochemical pathway is involved in MP-induced TNF production by THP-1 cells and that MP induce TNF production in the cells at the level of transcription. MP, unlike other bacteria, lack cell walls and lipopolysaccharide. The possible involvement of a TNF production mechanism distinct from that triggered by lipopolysaccharide is discussed.
我们证明,支原体(MP),此前已证明可增强小鼠腹腔巨噬细胞的抗肿瘤活性,也能在人单核细胞系THP-1中诱导细胞毒活性。MP以时间和剂量依赖的方式诱导THP-1细胞产生细胞毒活性。通过使用抗肿瘤坏死因子(TNF)抗体进行中和,显示细胞毒活性是由于MP刺激的细胞释放的TNF所致。对第二信使途径抑制剂的研究和Northern RNA印迹分析表明,一条Ca2+依赖而非蛋白激酶C依赖的生化途径参与了MP诱导THP-1细胞产生TNF的过程,并且MP在转录水平诱导细胞产生TNF。与其他细菌不同,MP没有细胞壁和脂多糖。本文讨论了可能存在不同于脂多糖触发机制的TNF产生机制。