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首页> 外文期刊>Microbes and infection >Toll-like receptor 2 (TLR2) and dectin-1 contribute to the production of IL-12p40 by bone marrow-derived dendritic cells infected with Penicillium marneffei.
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Toll-like receptor 2 (TLR2) and dectin-1 contribute to the production of IL-12p40 by bone marrow-derived dendritic cells infected with Penicillium marneffei.

机译:Toll样受体2(TLR2)和dectin-1有助于感染了马尔尼菲青霉的骨髓源性树突状细胞产生IL-12p40。

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摘要

The present study was designed to elucidate the role of TLR2, TLR4 and dectin-1 in the production of IL-12p40 by bone marrow-derived dendritic cells (BM-DCs) infected with Penicillium marneffei. IL-12p40 production was almost completely abrogated in BM-DCs from TLR2 gene-knockout (KO) and MyD88KO mice, but not from TLR4-defective C3H/HeJ mice compared to those from control mice. Furthermore, BM-DCs from dectin-1KO mice faintly produced IL-12p40 upon stimulation with this fungus. Using a luciferase reporter assay, P. marneffei activated NF-kappaB in HEK293 cells transfected with the TLR2 gene, but not with the dectin-1 gene, and their co-transfection did not lead to further increase in this response. These results indicate that TLR2 and dectin-1 are essential in sensing P. marneffei for the activation of BM-DCs.
机译:本研究旨在阐明TLR2,TLR4和dectin-1在感染了马尔尼菲青霉的骨髓源性树突状细胞(BM-DC)产生IL-12p40中的作用。与对照小鼠相比,TLR2基因敲除(KO)和MyD88KO小鼠的BM-DCs中IL-12p40的产生几乎完全被消除,而TLR4缺陷型C3H / HeJ小鼠的IL- 12p40的产生却几乎没有。此外,来自dectin-1KO小鼠的BM-DC在用这种真菌刺激后微弱地产生了IL-12p40。使用萤光素酶报告基因测定法,marneffei激活了用TLR2基因而非dectin-1基因转染的HEK293细胞中的NF-kappaB,并且它们的共转染并未导致这种反应的进一步增加。这些结果表明TLR2和dectin-1是必不可少的感测疟原虫对BM-DCs的激活。

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