Häcker H, Mischak H, Miethke T, Liptay S, Schmid R, Sparwasser T, Heeg K, Lipford G B, Wagner H
Institute of Medical Microbiology, Immunology and Hygiene, Technische Universität München, Trogerstrasse 9, D-81675 Munich, Germany.
EMBO J. 1998 Nov 2;17(21):6230-40. doi: 10.1093/emboj/17.21.6230.
Unmethylated CpG motifs in bacterial DNA, plasmid DNA and synthetic oligodeoxynucleotides (CpG ODN) activate dendritic cells (DC) and macrophages in a CD40-CD40 ligand-independent fashion. To understand the molecular mechanisms involved we focused on the cellular uptake of CpG ODN, the need for endosomal maturation and the role of the stress kinase pathway. Here we demonstrate that CpG-DNA induces phosphorylation of Jun N-terminal kinase kinase 1 (JNKK1/SEK/MKK4) and subsequent activation of the stress kinases JNK1/2 and p38 in murine macrophages and dendritic cells. This leads to activation of the transcription factor activating protein-1 (AP-1) via phosphorylation of its constituents c-Jun and ATF2. Moreover, stress kinase activation is essential for CpG-DNA-induced cytokine release of tumor necrosis factor alpha (TNFalpha) and interleukin-12 (IL-12), as inhibition of p38 results in severe impairment of this biological response. We further demonstrate that cellular uptake via endocytosis and subsequent endosomal maturation is essential for signalling, since competition by non-CpG-DNA or compounds blocking endosomal maturation such as chloroquine or bafilomycin A prevent all aspects of cellular activation. The data suggest that endosomal maturation is required for translation of intraendosomal CpG ODN sequences into signalling via the stress kinase pathway, where p38 kinase activation represents an essential step in CpG-ODN-triggered activation of antigen-presenting cells.
细菌DNA、质粒DNA和合成的寡脱氧核苷酸(CpG ODN)中的未甲基化CpG基序以不依赖CD40 - CD40配体的方式激活树突状细胞(DC)和巨噬细胞。为了了解其中涉及的分子机制,我们重点研究了CpG ODN的细胞摄取、内体成熟的必要性以及应激激酶途径的作用。在此我们证明,CpG - DNA可诱导小鼠巨噬细胞和树突状细胞中Jun N末端激酶激酶1(JNKK1/SEK/MKK4)的磷酸化,随后激活应激激酶JNK1/2和p38。这通过其组成成分c - Jun和ATF2的磷酸化导致转录因子激活蛋白-1(AP - 1)的激活。此外,应激激酶激活对于CpG - DNA诱导的肿瘤坏死因子α(TNFα)和白细胞介素-12(IL - 12)的细胞因子释放至关重要,因为抑制p38会导致这种生物学反应严重受损。我们进一步证明,通过内吞作用的细胞摄取以及随后的内体成熟对于信号传导至关重要,因为非CpG - DNA或阻断内体成熟的化合物(如氯喹或巴弗洛霉素A)的竞争会阻止细胞激活的所有方面。数据表明,内体成熟对于将内体中的CpG ODN序列转化为通过应激激酶途径的信号传导是必需的,其中p38激酶激活代表CpG - ODN触发抗原呈递细胞激活的关键步骤。