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去甲斑蝥素通过上调巨噬细胞中 AKT/NF-κB 信号通路促进 LPS 介导的免疫反应。

Norcantharidin facilitates LPS-mediated immune responses by up-regulation of AKT/NF-κB signaling in macrophages.

机构信息

Shanghai Key Laboratory of Regulatory Biology, Institute of Biomedical Sciences and School of Life Sciences, East China Normal University, Shanghai, China.

出版信息

PLoS One. 2012;7(9):e44956. doi: 10.1371/journal.pone.0044956. Epub 2012 Sep 11.

Abstract

Norcantharidin (NCTD), a demethylated analog of cantharidin, is a common used clinical drug to inhibit proliferation and metastasis of cancer cells. But the role of NCTD in modulating immune responses remains unknown. Here, we investigated the function and mechanism of NCTD in regulation of TLR4 associated immune response in macrophages. We evaluated the influence of NCTD on host defense against invaded pathogens by acute peritonitis mouse model, ELISA, Q-PCR, nitrite quantification, phagocytosis assay and gelatin zymography assay. Our data showed that the survival and the serum concentrations of IL-6 and TNF-α were all enhanced by NCTD significantly in peritonitis mouse model. Accordingly, LPS-induced cytokine, nitric oxide and MMP-9 production as well as the phagocytosis of bacteria were all up-regulated by NCTD in a dose dependent manner in both RAW264.7 cells and bone marrow-derived macrophages (BMMs). Then we further analyzed TLR4 associated signaling pathway by Western blot, Immunofluorescence and EMSA in the presence or absence of LPS. The phosphorylation of AKT and p65 at serine 536 but not serine 468 was enhanced obviously by NCTD in a dose dependent manner, whereas the degradation of IκBα was little effected. Consequently, the nuclear translocation and DNA binding ability of NF-κB was also increased by NCTD obviously in RAW264.7 cells. Our results demonstrated that NCTD could facilitate LPS-mediated immune response through promoting the phosphorylation of AKT/p65 and transcriptional activity of NF-κB, thus reprofiling the traditional anti-tumor drug NCTD as a novel immune regulator in promoting host defense against bacterial infection.

摘要

去甲基斑蝥素(NCTD)是斑蝥素的一种脱甲基类似物,是一种常用于抑制癌细胞增殖和转移的临床药物。但 NCTD 调节免疫反应的作用尚不清楚。在这里,我们研究了 NCTD 在调节巨噬细胞 TLR4 相关免疫反应中的功能和机制。我们通过急性腹膜炎小鼠模型、ELISA、Q-PCR、亚硝酸盐定量、吞噬试验和明胶酶谱分析评估了 NCTD 对宿主抵御入侵病原体的影响。我们的数据表明,NCTD 显著增强了腹膜炎小鼠模型中的存活和血清中白细胞介素-6 和肿瘤坏死因子-α的浓度。相应地,NCTD 以剂量依赖的方式上调了 LPS 诱导的细胞因子、一氧化氮和 MMP-9 的产生以及细菌的吞噬作用,无论是在 RAW264.7 细胞还是骨髓来源的巨噬细胞(BMM)中。然后,我们通过 Western blot、免疫荧光和 EMSA 在 LPS 存在或不存在的情况下进一步分析了 TLR4 相关信号通路。NCTD 明显地以剂量依赖的方式增强了 AKT 和 p65 丝氨酸 536 的磷酸化,但对丝氨酸 468 没有影响,而 IκBα 的降解则影响不大。因此,NCTD 明显增加了 NF-κB 的核易位和 DNA 结合能力。我们的结果表明,NCTD 可以通过促进 AKT/p65 的磷酸化和 NF-κB 的转录活性,促进 LPS 介导的免疫反应,从而将传统的抗肿瘤药物 NCTD 重新定义为一种促进宿主抵御细菌感染的新型免疫调节剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de07/3439369/69f7b17b9455/pone.0044956.g001.jpg

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