Low-Dose Lipopolysaccharide Modifies the Production of IL-12 by Dendritic Cells in Response to Various Cytokines
-
- Saito Yusuke
- Division of Immunobiology, Institute for Genetic Medicine, Hokkaido University
-
- Yanagawa Yoshiki
- Division of Immunobiology, Institute for Genetic Medicine, Hokkaido University
-
- Kikuchi Kazuhiro
- Division of Immunobiology, Institute for Genetic Medicine, Hokkaido University
-
- Iijima Norifumi
- Division of Immunobiology, Institute for Genetic Medicine, Hokkaido University
-
- Iwabuchi Kazuya
- Division of Immunobiology, Institute for Genetic Medicine, Hokkaido University
-
- Onoé Kazunori
- Division of Immunobiology, Institute for Genetic Medicine, Hokkaido University
この論文をさがす
抄録
Dendritic cell (DC) activation is triggered by cytokines, including tumor necrosis factor (TNF)-α, and microbe components, including lipopolysaccharide (LPS). During the initial stage of infection, the microbe components appear to be present at low concentration. To determine the role of low-dose microbe-components in DC activation during the initial stage of infection, we examined the effects of low-dose LPS on cytokine-induced maturation and function of DCs. Low-dose LPS (1 ng/ml) treatment of DCs had only additive effects on the expression of CD86 and major histocompatibility complex class II induced by various cytokines, including interleukin (IL)-1β, TNF-α and interferon (IFN)-γ. IL-1β alone significantly induced IL-12 production in DCs, whereas TNF-α or IFN-γ induced modest levels of IL-12 production. When low-dose LPS (1 ng/ml), which only slightly induced IL-12 production, was added to the culture, only an additive effect was seen on IL-1β-induced IL-12 production. In contrast, low-dose LPS synergistically enhanced TNF-α- or IFN-γ-induced IL-12 production. SB203580, a specific inhibitor of p38 MAPK, markedly inhibited TNF-α- or IFN-γ-induced IL-12-production either in the absence or presence of LPS, but showed only modest effects on IL-1β-induced IL-12-production. These findings suggest that the p38 MAPK pathway is essential for the synergistic IL-12 production induced by TNF-α- or IFN-γ in combination with low-dose LPS in DC.
収録刊行物
-
- Journal of Clinical and Experimental Hematopathology
-
Journal of Clinical and Experimental Hematopathology 46 (1), 31-36, 2006
日本リンパ網内系学会
- Tweet
詳細情報 詳細情報について
-
- CRID
- 1390282679678167680
-
- NII論文ID
- 10018113770
-
- NII書誌ID
- AA11556796
-
- ISSN
- 18809952
- 13464280
-
- 本文言語コード
- en
-
- データソース種別
-
- JaLC
- Crossref
- CiNii Articles
-
- 抄録ライセンスフラグ
- 使用不可