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毒性小分子引发的差异化炎症反应。

Differential inflammatory responses triggered by toxic small molecules.

机构信息

Department of Microbiology and Immunology, The University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA.

出版信息

Environ Sci Pollut Res Int. 2012 Mar;19(3):619-27. doi: 10.1007/s11356-011-0593-2. Epub 2011 Sep 1.

Abstract

PURPOSE

The aim of this study is to determine whether exposure to hazardous chemicals alters chemokine or cytokine production in macrophages and link these events to changes in intracellular signaling pathways and activation of specific gene promoters.

METHODS

RAW 264.7 mouse macrophages were treated with selected toxic industrial chemicals (TICs) and examined for changes in immune function. Luminex multiplex technology was used to assess changes in cytokine/chemokine expression and activation of kinase signaling pathways. In addition, a panel of macrophage cell lines with promoter-specific luciferase reporter genes were generated and treated with the TICs, and transcriptional responses to these chemicals were detected by changes in luminescence.

RESULTS

Changes in expression of cytokines and chemokines were linked to changes in the activation state of intracellular signaling pathways. Overall, the findings reveal that sublytic levels of TICs can alter the profile of cytokines and chemokines expressed by macrophages, with a pattern that suggests immunosuppression. The data demonstrate that critical changes in immune function correlate with activation of kinase signaling pathways in macrophages.

CONCLUSIONS

These data provide insight into the effects of sublytic doses of selected TICs on macrophage function, with a particular emphasis on identifying changes in expression of cytokines and chemokines. These altered patterns in immune function were linked to changes in the activation state of intracellular signaling pathways. The data strongly suggest that small amounts of TICs can have subtle, yet very critical, effects on macrophages.

摘要

目的

本研究旨在确定接触有害化学物质是否会改变巨噬细胞中趋化因子或细胞因子的产生,并将这些事件与细胞内信号通路的变化和特定基因启动子的激活联系起来。

方法

用选定的有毒工业化学品(TICs)处理 RAW 264.7 小鼠巨噬细胞,并检查其免疫功能的变化。采用Luminex 多重技术评估细胞因子/趋化因子表达的变化和激酶信号通路的激活。此外,还生成了一组具有启动子特异性荧光素酶报告基因的巨噬细胞细胞系,并用 TICs 处理这些细胞系,通过发光变化检测这些化学物质的转录反应。

结果

细胞因子和趋化因子表达的变化与细胞内信号通路激活状态的变化有关。总的来说,这些发现表明,亚致死水平的 TICs 可以改变巨噬细胞表达的细胞因子和趋化因子的谱,表明免疫抑制。数据表明,免疫功能的关键变化与巨噬细胞中激酶信号通路的激活相关。

结论

这些数据深入了解了选定 TICs 的亚致死剂量对巨噬细胞功能的影响,特别强调了细胞因子和趋化因子表达的变化。这些免疫功能的改变模式与细胞内信号通路激活状态的变化有关。数据强烈表明,少量 TICs 可以对巨噬细胞产生微妙但非常关键的影响。

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