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鼠李糖乳杆菌 GR-1 暴露后粒细胞集落刺激因子在巨噬细胞-树突状细胞相互作用中的抗炎作用。

The anti-inflammatory role of granulocyte colony-stimulating factor in macrophage-dendritic cell crosstalk after Lactobacillus rhamnosus GR-1 exposure.

机构信息

Department of Microbiology and Immunology, University of Western Ontario, London, Ontario, N6G 2V4, Canada.

出版信息

J Leukoc Biol. 2011 Jun;89(6):907-15. doi: 10.1189/jlb.0810445. Epub 2011 Mar 8.

Abstract

MΦs are important sensory cells of the innate immune system and regulate immune responses through releasing different combinations of cytokines. In this study, we examined whether cytokines released by MΦs in response to the probiotic bacterial strain GR-1 modulate the responses of DCs. The cytokine profile released by GR-1-treated MΦs was characterized by low levels of TNF-α, GM-CSF, IL-6, and IL-12 but very high levels of G-CSF. GR-1 CM did not induce expression of the shared p40 subunit of IL-12 and IL-23 and costimulatory molecules CD80 or CD86 or increase T cell stimulatory capacity in DCs. However, in G-CSFR-deficient DCs or after antibody-mediated neutralization of G-CSF, GR-1 CM induced IL-12/23 p40 production significantly, indicating that G-CSF within the GR-1 CM inhibits IL-12/23 p40 production induced by other CM components. GR-1 CM and rG-CSF also inhibited LPS-induced IL-12 production at the mRNA and protein levels. The inhibition of IL-12 production by G-CSF was at least in part mediated through inhibition of JNK activation. Finally, splenic DCs of GR-1-injected mice produced less IL-12/23 p40 than those of PBS-injected mice in response to LPS ex vivo, and this was at least partially dependent on exposure to GR-1-induced G-CSF in vivo. Altogether, these results suggest that G-CSF modulates the IL-12/23 p40 response of DCs in the context of the probiotic GR-1 through MΦ-DC crosstalk.

摘要

MΦs 是先天免疫系统的重要感应细胞,通过释放不同组合的细胞因子来调节免疫反应。在这项研究中,我们研究了 GR-1 益生菌菌株刺激的 MΦs 释放的细胞因子是否调节 DC 反应。GR-1 处理的 MΦ 释放的细胞因子谱特征为 TNF-α、GM-CSF、IL-6 和 IL-12 水平较低,但 G-CSF 水平非常高。GR-1 CM 不会诱导 IL-12 和 IL-23 的共享 p40 亚基以及共刺激分子 CD80 或 CD86 的表达,也不会增加 DC 中的 T 细胞刺激能力。然而,在 G-CSFR 缺陷型 DC 或在 G-CSF 抗体中和后,GR-1 CM 显著诱导 IL-12/23 p40 产生,表明 GR-1 CM 中的 G-CSF 抑制了由其他 CM 成分诱导的 IL-12/23 p40 产生。GR-1 CM 和 rG-CSF 还抑制 LPS 诱导的 IL-12 产生在 mRNA 和蛋白水平。G-CSF 抑制 IL-12 产生至少部分是通过抑制 JNK 激活介导的。最后,GR-1 注射小鼠的脾 DC 产生的 IL-12/23 p40 比 PBS 注射小鼠在 LPS 体外刺激时产生的少,这至少部分依赖于体内暴露于 GR-1 诱导的 G-CSF。总之,这些结果表明 G-CSF 通过 MΦ-DC 串扰调节益生菌 GR-1 背景下的 DC 中的 IL-12/23 p40 反应。

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