Aosai Fumie, Rodriguez Pena Martha S, Mun Hye-Seong, Fang Hao, Mitsunaga Tetsuya, Norose Kazumi, Kang Hyun Kyu, Bae Yoe-Sik, Yano Akihiko
Department of Infection and Host Defense, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chuoku, Chiba 260-8670, Japan.
Cell Stress Chaperones. 2006 Spring;11(1):13-22. doi: 10.1379/csc-138r.1.
Toxoplasma gondii-derived heat shock protein 70 (T.g.HSP70) induced maturation of bone marrow-derived dendritic cells (DCs) of wild-type (WT) C57BL/6 mice as evidenced by an increase in surface expression of MHC class I and II molecules and costimulatory molecules such as CD40, CD80, and CD86. Functionally, decreased phagocytic ability and increased alloreactive T cell stimulatory ability were observed in T.g.HSP70-stimulated DCs. These phenotypic and functional changes of T.g.HSP70-stimulated DCs were demonstrated in Toll-like receptor (TLR) 2- and myeloid differentiation factor 88 (MyD88)-deficient but not TLR4-deficient C57BL/6 mice. DCs from WT and TLR2-deficient but not TLR4-deficient mice produced IL-12 after T.g.HSP70 stimulation. T.g.HSP70-stimulated DCs from WT, TLR2-deficient, and MyD88-deficient, but not TLR4-deficient mice expressed IFN-beta mRNA. Thus, T.g.HSP70 stimulates murine DC maturation via TLR4 through the MyD88-independent signal transduction cascade.
刚地弓形虫来源的热休克蛋白70(T.g.HSP70)可诱导野生型(WT)C57BL/6小鼠骨髓来源的树突状细胞(DCs)成熟,这可通过MHC I类和II类分子以及共刺激分子如CD40、CD80和CD86表面表达的增加得以证明。在功能上,在T.g.HSP70刺激的DCs中观察到吞噬能力下降和同种异体反应性T细胞刺激能力增强。T.g.HSP70刺激的DCs的这些表型和功能变化在Toll样受体(TLR)2和髓样分化因子88(MyD88)缺陷的C57BL/6小鼠中得到证实,但在TLR4缺陷的小鼠中未得到证实。来自野生型和TLR2缺陷但非TLR4缺陷小鼠的DCs在T.g.HSP70刺激后产生IL-12。来自野生型、TLR2缺陷和MyD88缺陷但非TLR4缺陷小鼠的T.g.HSP70刺激的DCs表达IFN-β mRNA。因此,T.g.HSP70通过MyD88非依赖的信号转导级联反应经由TLR4刺激小鼠DC成熟。