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首页> 外文期刊>Infection and immunity >Discordance in the Effects of Yersinia pestis on the Dendritic Cell Functions Manifested by Induction of Maturation and Paralysis of Migration
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Discordance in the Effects of Yersinia pestis on the Dendritic Cell Functions Manifested by Induction of Maturation and Paralysis of Migration

机译:鼠疫耶尔森氏菌对诱导成熟和迁移麻痹表现出的树突状细胞功能的影响不一致

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The encounter between invading microorganisms and dendritic cells (DC) triggers a series of events which include uptake and degradation of the microorganism, induction of a maturation process, and enhancement of DC migration to the draining lymph nodes. Various pathogens have developed strategies to counteract these events as a measure to evade the host defense. In the present study we found that interaction of the Yersinia pestis EV76 strain with DC has no effect on cell viability and is characterized by compliance with effective maturation, which is manifested by surface display of major histocompatibility complex class II, of costimulatory markers, and of the chemokine receptor CCR7. This is in contrast to maturation inhibition and cell death induction exerted by the related species Yersinia enterocolitica WA O:8. Y. pestis interactions with DC were found, however, to impair functions related to cytoskeleton rearrangement. DC pulsed with Y. pestis failed to adhere to solid surfaces and to migrate toward the chemokine CCL19 in an in vitro transmembrane assay. Both effects were dependent on the presence of the pCD1 virulence plasmid and on a bacterial growth shift to 37°C prior to infection. Moreover, while instillation of a pCD1-cured Y. pestis strain into mouse airways triggered effective transport of alveolar DC to the mediastinal lymph node, instillation of Y. pestis harboring the plasmid failed to do so. Taken together, these results suggest that virulence plasmid-dependent impairment of DC migration is the major mechanism utilized by Y. pestis to subvert DC function.
机译:入侵的微生物与树突状细胞(DC)之间的相遇触发了一系列事件,包括微生物的摄取和降解,诱导成熟过程以及增强DC向引流淋巴结的迁移。各种病原体已经开发出应对这些事件的策略,以此作为逃避宿主防御的措施。在本研究中,我们发现鼠伤寒耶尔森氏菌EV76菌株与DC的相互作用对细胞活力没有影响,并且以有效成熟的顺应性为特征,这表现在主要组织相容性复合物II类表面显示,共刺激标记和趋化因子受体CCR7。这与相关物种 Enterocolitica WA O:8的成熟抑制和细胞死亡诱导相反。是的然而发现与DC的瘟疫相互作用会削弱与细胞骨架重排有关的功能。用 Y脉冲的DC。在体外跨膜测定中,瘟疫杆菌不能粘附在固体表面上并迁移至趋化因子CCL19。两种作用均取决于pCD1毒力质粒的存在以及感染前细菌向37°C的生长转移。而且,在滴注pCD1固化的 Y时。鼠疫中的鼠疫菌株触发了肺泡DC到纵隔淋巴结的有效转运,并注入了 Y。携带该质粒的瘟疫菌未能成功。两者合计,这些结果表明毒力质粒依赖的DC迁移的损害是 Y利用的主要机制。瘟病颠覆直流功能。

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