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淋巴细胞性脉络丛脑膜炎病毒感染树突状细胞以不依赖于白细胞介素-10 的方式干扰 TLR 诱导的白细胞介素-12/白细胞介素-23 细胞因子的产生。

Lymphocytic choriomeningitis virus infection of dendritic cells interferes with TLR-induced IL-12/IL-23 cytokine production in an IL-10 independent manner.

机构信息

Department of Biomedical and Molecular Sciences, Queen's University, Kingston, Canada.

Department of Biomedical and Molecular Sciences, Queen's University, Kingston, Canada.

出版信息

Cytokine. 2018 Aug;108:105-114. doi: 10.1016/j.cyto.2018.03.017. Epub 2018 Mar 27.

Abstract

Dendritic cells produce IL-12 and IL-23 in response to viral and bacterial infection and these cytokines are responsible for successful pathogen clearance. How sequential viral and bacterial infections affect the production of IL-12 and IL-23 is currently not known. Our study demonstrates that in dendritic cells infected with Lymphocytic choriomeningitis virus (LCMV), TLR activation with bacterial PAMPs resulted in reduced IL-12 and IL-23 expression compared to non-infected cells. Furthermore, expression of other proinflammatory cytokines, TNF-α and IL-6, were not inhibited under these conditions. We discovered that TLR-induced phosphorylation of p38 was significantly inhibited in LCMV-infected cells. We detected enhanced expression of suppressor of cytokine signalling (SOCS)-3 and IL-10. Yet, neutralizing IL-10 did not restore IL-12/IL-23 expression. Taken together, these results show that virus infection interferes with the magnitude of TLR-mediated inflammatory responses by repressing specific cytokine expression.

摘要

树突状细胞在受到病毒和细菌感染时会产生 IL-12 和 IL-23,这些细胞因子对于成功清除病原体至关重要。目前尚不清楚连续的病毒和细菌感染如何影响 IL-12 和 IL-23 的产生。我们的研究表明,在感染淋巴细胞性脉络丛脑膜炎病毒 (LCMV) 的树突状细胞中,与非感染细胞相比,细菌 PAMP 的 TLR 激活导致 IL-12 和 IL-23 的表达减少。此外,在这些条件下,其他促炎细胞因子 TNF-α和 IL-6 的表达并未受到抑制。我们发现,LCMV 感染细胞中 TLR 诱导的 p38 磷酸化明显受到抑制。我们检测到细胞因子信号转导抑制剂 (SOCS)-3 和 IL-10 的表达增强。然而,中和 IL-10 并不能恢复 IL-12/IL-23 的表达。综上所述,这些结果表明病毒感染通过抑制特定细胞因子的表达来干扰 TLR 介导的炎症反应的幅度。

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