Kaufmann A, Mühlradt P F, Gemsa D, Sprenger H
Institute of Immunology, Philipps University, Marburg, Germany.
Infect Immun. 1999 Dec;67(12):6303-8. doi: 10.1128/IAI.67.12.6303-6308.1999.
Bacterial infections are characterized by strong inflammatory reactions. The responsible mediators are often bacterially derived cell wall molecules, such as lipopolysaccharide or lipoteichoic acids, which typically stimulate monocytes and macrophages to release a wide variety of inflammatory cytokines and chemokines. Mycoplasmas, which lack a cell wall, may also stimulate monocytes very efficiently. This study was performed to identify mycoplasma-induced mediators. We investigated the induction of cytokines and chemokines in human monocytes exposed to the Mycoplasma fermentans-derived membrane component MALP-2 (macrophage-activating lipopeptide 2) by dose response and kinetic analysis. We found a rapid and strong MALP-2-inducible chemokine and cytokine gene expression which was followed by the release of chemokines and cytokines with peak levels after 12 to 20 h. MALP-2 induced the neutrophil-attracting CXC chemokines interleukin-8 (IL-8) and GRO-alpha as well as the mononuclear leukocyte-attracting CC chemokines MCP-1, MIP-1alpha, and MIP-1beta. Production of the proinflammatory cytokines tumor necrosis factor alpha and IL-6 started at the same time as chemokine release but required 10- to 100-fold-higher MALP-2 doses. The data show that the mycoplasma-derived lipopeptide MALP-2 represents a potent inducer of chemokines and cytokines which may, by the attraction and activation of neutrophils and mononuclear leukocytes, significantly contribute to the inflammatory response during mycoplasma infection.
细菌感染的特征是强烈的炎症反应。起作用的介质通常是细菌来源的细胞壁分子,如脂多糖或脂磷壁酸,它们通常刺激单核细胞和巨噬细胞释放多种炎性细胞因子和趋化因子。缺乏细胞壁的支原体也可能非常有效地刺激单核细胞。进行这项研究以鉴定支原体诱导的介质。我们通过剂量反应和动力学分析,研究了暴露于发酵支原体来源的膜成分MALP-2(巨噬细胞激活脂肽2)的人单核细胞中细胞因子和趋化因子的诱导情况。我们发现MALP-2可快速且强烈地诱导趋化因子和细胞因子基因表达,随后趋化因子和细胞因子释放,在12至20小时后达到峰值水平。MALP-2诱导吸引中性粒细胞的CXC趋化因子白细胞介素-8(IL-8)和GRO-α,以及吸引单核白细胞的CC趋化因子MCP-1、MIP-1α和MIP-1β。促炎细胞因子肿瘤坏死因子α和IL-6的产生与趋化因子释放同时开始,但所需的MALP-2剂量要高10至100倍。数据表明,支原体来源的脂肽MALP-2是趋化因子和细胞因子的有效诱导剂,通过吸引和激活中性粒细胞和单核白细胞,可能在支原体感染期间的炎症反应中起重要作用。