Yamamoto Y, Klein T W, Friedman H
Department of Medical Microbiology and Immunology, University of South Florida College of Medicine, Tampa 33612, USA.
Infect Immun. 1996 Aug;64(8):3062-8. doi: 10.1128/iai.64.8.3062-3068.1996.
The attachment of bacteria to macrophages is mediated by different ligands and receptors and induces various intracellular molecular responses. In the present study, induction of cytokines and chemokines, especially granulocyte-macrophage colony-stimulating factor (GM-CSF) and macrophage inflammatory protein 2 (MIP-2), was examined, following bacterial attachment, with regard to the ligand-receptor systems involved. Attachment of Legionella pneumophila or Salmonella typhimurium to cultured mouse peritoneal macrophages increased the steady-state levels of cellular mRNAs for the cytokines interleukin 1beta (IL-1beta), IL-6, and GM-CSF as well as the chemokines MIP-1beta, MIP-2, and KC. However, when macrophages were treated with alpha-methyl-D-mannoside (alphaMM), a competitor of glycopeptide ligands, induction of cytokine mRNAs was inhibited, but the levels of chemokine mRNAs were not. Pretreatment of the bacteria with fresh mouse serum enhanced the level of GM-CSF mRNA but not the level of MIP-2 mRNA. In addition, serum treatment reduced the inhibitory effect of alphaMM on GM-CSF mRNA. These results indicate that bacterial attachment increases the steady-state levels of the cytokine and chemokine mRNAs tested by at least two distinct receptor-ligand systems, namely, one linked to cytokine induction and involving mannose or other sugar residues and the other linked to chemokine induction and relatively alphaMM insensitive. Furthermore, opsonization with serum engages other pathways in the cytokine response which are relatively independent of the alphaMM-sensitive system. Regarding bacterial surface ligands involved in cytokine mRNA induction, evidence is presented that the flagellum may be important in stimulating cytokine GM-CSF message but not chemokine MIP-2 message. Analysis of cytokine GM-CSF and chemokine MIP-2 signaling pathways with protein kinase inhibitors revealed the involvement of calmodulin and myosin light-chain kinase in GM-CSF but not MIP-2 mRNA induction, adding further evidence that several distinct receptor systems are engaged during the process of bacterial attachment and induction of cytokines and chemokines, such as GM-CSF and MIP-2, respectively.
细菌与巨噬细胞的附着由不同的配体和受体介导,并诱导各种细胞内分子反应。在本研究中,在细菌附着后,针对所涉及的配体 - 受体系统,检测了细胞因子和趋化因子的诱导情况,特别是粒细胞 - 巨噬细胞集落刺激因子(GM - CSF)和巨噬细胞炎性蛋白2(MIP - 2)。嗜肺军团菌或鼠伤寒沙门氏菌与培养的小鼠腹腔巨噬细胞的附着增加了细胞因子白细胞介素1β(IL - 1β)、IL - 6和GM - CSF以及趋化因子MIP - 1β、MIP - 2和KC的细胞mRNA稳态水平。然而,当巨噬细胞用糖肽配体的竞争者α - 甲基 - D - 甘露糖苷(αMM)处理时,细胞因子mRNA的诱导受到抑制,但趋化因子mRNA的水平未受影响。用新鲜小鼠血清预处理细菌可提高GM - CSF mRNA的水平,但不提高MIP - 2 mRNA的水平。此外,血清处理降低了αMM对GM - CSF mRNA的抑制作用。这些结果表明,细菌附着通过至少两种不同的受体 - 配体系统增加了所检测的细胞因子和趋化因子mRNA的稳态水平,即一种与细胞因子诱导相关且涉及甘露糖或其他糖残基,另一种与趋化因子诱导相关且对αMM相对不敏感。此外,血清调理作用参与了细胞因子反应中的其他途径,这些途径相对独立于αMM敏感系统。关于参与细胞因子mRNA诱导的细菌表面配体,有证据表明鞭毛可能在刺激细胞因子GM - CSF信息传递方面很重要,但在趋化因子MIP - 2信息传递方面不重要。用蛋白激酶抑制剂分析细胞因子GM - CSF和趋化因子MIP - 2信号通路发现,钙调蛋白和肌球蛋白轻链激酶参与GM - CSF而非MIP - 2 mRNA的诱导,进一步证明在细菌附着以及细胞因子和趋化因子(如GM - CSF和MIP - 2)诱导过程中涉及几种不同的受体系统。