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首页> 外文期刊>Microbial Pathogenesis >Migration of Salmonella typhimurioum-harboring bone marrow-derived dendritic cells towards the chemokines CCL19 and CCL21
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Migration of Salmonella typhimurioum-harboring bone marrow-derived dendritic cells towards the chemokines CCL19 and CCL21

机译:携带鼠伤寒沙门氏菌的骨髓树突状细胞向趋化因子CCL19和CCL21的迁移

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Macrophages are considered as main cellular target encountered by the facultative intracellular bacterium Salmonella typhimurium. However, in orally infected mice these pathogens are first internalized by dendritic cells (DCs) that are located in the subepithelial dome of Peyer's patches. Moreover, DCs can penetrate the intestinal epithelium to sample bacteria. Here, we examined the interaction of Salmonella with bone marrow-derived DCs (BM-DCs). In order to study the role of DCs as vehicles for the dissemination of Salmonella, an in vitro model was established. In this model, Salmonella-activated BM-DCs enhanced surface expression of MHC class II and costimulatory molecules. We found that, upon maturation, BM-DCs upregulated chemokine receptor 7 (CCR7) mRNA and surface molecule expression. Salmonella-exposed DCs as well as mature DCs, but not immature DCs, were recruited towards the CC chemokines CCL19 and CCL21, two ligands of CCR7. The maturation process of DCs did neither require bacterial internalization nor viability. About one third of the migrated BM-DCs harbored intracellular bacteria, whereas the remaining two third did not contain bacteria. Salmonella, but not an apathogenic E. coli laboratory strain was capable to survive within BM-DCs. Taken together, our data implicate that DCs are first activated and subsequently utilized as carriers by Salmonella.
机译:巨噬细胞被认为是兼性细胞内鼠伤寒沙门氏菌遇到的主要细胞靶标。但是,在口腔感染的小鼠中,这些病原体首先被位于Peyer斑块上皮下圆顶的树突状细胞(DC)内化。此外,DC可以穿透肠道上皮来取样细菌。在这里,我们检查了沙门氏菌与骨髓源DC(BM-DC)的相互作用。为了研究DC作为沙门氏菌传播媒介的作用,建立了体外模型。在此模型中,沙门氏菌激活的BM-DC增强了II类MHC和共刺激分子的表面表达。我们发现,成熟后,BM-DCs上调趋化因子受体7(CCR7)mRNA和表面分子表达。沙门氏菌暴露的DC以及成熟的DC,但未成熟的DC被招募到CC趋化因子CCL19和CCL21(CCR7的两个配体)。 DC的成熟过程既不需要细菌内在化也不需要生存力。迁移的BM-DC中约有三分之一携带细胞内细菌,而其余的三分之二则不含细菌。沙门氏菌能在BM-DCs中存活,但不能杀死大肠杆菌。综上所述,我们的数据表明,沙门氏菌首先激活了DC,随后又将其用作载体。

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