首页> 外文OA文献 >Plasminogen Activator Pla of Yersinia pestis Utilizes Murine DEC-205 (CD205) as a Receptor to Promote Dissemination*
【2h】

Plasminogen Activator Pla of Yersinia pestis Utilizes Murine DEC-205 (CD205) as a Receptor to Promote Dissemination*

机译:鼠疫耶尔森氏菌的纤溶酶原激活剂Pla利用鼠类 DEC-205(CD205)作为促进受体 传播*

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Yersinia pestis, a Gram-negative bacterium that causes bubonic and pneumonic plague, is able to rapidly disseminate to other parts of its mammalian hosts. Y. pestis expresses plasminogen activator (PLA) on its surface, which has been suggested to play a role in bacterial dissemination. It has been speculated that Y. pestis hijacks antigen-presenting cells, such as macrophages (MΦs) and dendritic cells, to be delivered to lymph nodes to initiate dissemination and infection. Both alveolar MΦs and pulmonary dendritic cells express a C-type lectin receptor, DEC-205 (CD205), which mediates antigen uptake and presentation. However, no ligand has been identified for DEC-205. In this study, we show that the invasion of alveolar MΦsby Y. pestis depends both in vitro and in vivo on the expression of PLA. DEC-205-expressing MΦs and transfectants, but not their negative counterparts, phagocytosed PLA-expressing Y. pestis and Escherichia coli K12 more efficiently than PLA-negative controls. The interactions between PLA-expressing bacteria and DEC-205-expressing transfectants or alveolar MΦs could be inhibited by an anti-DEC-205 antibody. Importantly, the blockage of the PLA-DEC-205 interaction reduced the dissemination of Y. pestis in mice. In conclusion, murine DEC-205 is a receptor for PLA of Y. pestis, and this host-pathogen interaction appears to play a key role in promoting bacterial dissemination.
机译:鼠疫耶尔森氏菌是一种革兰氏阴性细菌,可引起鼠疫和肺炎鼠疫,能够迅速传播到其哺乳动物宿主的其他部位。鼠疫耶尔森氏菌在其表面表达纤溶酶原激活剂(PLA),已被认为在细菌传播中起作用。据推测,鼠疫耶尔森氏菌劫持了抗原呈递细胞,例如巨噬细胞(MΦs)和树突状细胞,将其递送至淋巴结以开始传播和感染。肺泡MΦ和肺树突状细胞均表达C型凝集素受体DEC-205(CD205),介导抗原的摄取和呈递。但是,尚未确定DEC-205的配体。在这项研究中,我们表明,鼠疫耶尔森氏菌对肺泡MΦs的侵袭在体内和体外均取决于PLA的表达。表达DEC-205的MΦ和转染子,而不是它们的阴性对应物,比PLA阴性对照更有效地吞噬表达PLA的鼠疫耶尔森氏菌和大肠杆菌K12。表达PLA的细菌与表达DEC-205的转染子或肺泡MΦ之间的相互作用可以被抗DEC-205抗体抑制。重要的是,PLA-DEC-205相互作用的阻断减少了鼠疫耶尔森氏菌在小鼠中的传播。总之,鼠DEC-205是鼠疫耶尔森氏菌的PLA受体,这种宿主与病原体的相互作用似乎在促进细菌传播中起关键作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号