Vabulas R M, Ahmad-Nejad P, da Costa C, Miethke T, Kirschning C J, Häcker H, Wagner H
Institute of Medical Microbiology, Immunology and Hygiene, Technical University of Munich, Trogerstr. 9, 81675 Munich, Germany.
J Biol Chem. 2001 Aug 17;276(33):31332-9. doi: 10.1074/jbc.M103217200. Epub 2001 Jun 11.
Heat shock proteins (HSPs) require no adjuvant to confer immunogenicity to bound peptides, as if they possessed an intrinsic "danger" signature. To understand the proinflammatory nature of HSP, we analyzed signaling induced by human and chlamydial HSP60. We show that both HSP60s activate the stress-activated protein kinases p38 and JNK1/2, the mitogen-activated protein kinases ERK1/2, and the I-kappaB kinase (IKK). Activation of JNK and IKK proceeds via the Toll/IL-1 receptor signaling pathway involving MyD88 and TRAF6. Human fibroblasts transfected with TLR2 or TLR4 plus MD-2 gain responsiveness to HSP60, while TLR2- or TLR4-defective cells display impaired responses. Initiation of signaling requires endocytosis of HSP60 that is effectively inhibited by serum component(s). The results revealed that adjuvanticity of HSP60 operates similar to that of classical pathogen-derived ligands.
热休克蛋白(HSPs)无需佐剂就能赋予与之结合的肽免疫原性,就好像它们具有内在的“危险”信号。为了解热休克蛋白的促炎特性,我们分析了人源和衣原体热休克蛋白60(HSP60)诱导的信号传导。我们发现,这两种HSP60均能激活应激激活蛋白激酶p38和JNK1/2、丝裂原激活蛋白激酶ERK1/2以及IκB激酶(IKK)。JNK和IKK的激活通过涉及MyD88和TRAF6的Toll/IL-1受体信号通路进行。用TLR2或TLR4加MD-2转染的人成纤维细胞对HSP60产生反应,而TLR2或TLR4缺陷的细胞反应受损。信号传导的启动需要HSP60的内吞作用,而血清成分能有效抑制这种作用。结果表明,HSP60的佐剂活性与经典病原体衍生配体的佐剂活性相似。