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洋葱伯克霍尔德菌新型cepacia菌ET12菌株激活囊性纤维化气道上皮细胞中的TNFR1信号传导。

Burkholderia cenocepacia ET12 strain activates TNFR1 signalling in cystic fibrosis airway epithelial cells.

作者信息

Sajjan Umadevi S, Hershenson Marc B, Forstner Janet F, LiPuma John J

机构信息

Department of Pediatrics and Communicable Diseases, University of Michigan Medical School, 1150 W. Medical Center Drive, Ann Arbor, MI 48109, USA.

出版信息

Cell Microbiol. 2008 Jan;10(1):188-201. doi: 10.1111/j.1462-5822.2007.01029.x. Epub 2007 Aug 14.

Abstract

Burkholderia cenocepacia is an important pulmonary pathogen in individuals with cystic fibrosis (CF). Infection is often associated with severe pulmonary inflammation, and some patients develop a fatal necrotizing pneumonia and sepsis ('cepacia syndrome'). The mechanisms by which this species causes severe pulmonary inflammation are poorly understood. Here, we demonstrate that B. cenocepacia BC7, a potentially virulent representative of the epidemic ET12 lineage, binds to tumour necrosis factor receptor 1 (TNFR1) and activates TNFR1-related signalling pathway similar to TNF-alpha, a natural ligand for TNFR1. This interaction participates in stimulating a robust IL-8 production from CF airway epithelial cells. In contrast, BC45, a less virulent ET12 representative, and ATCC 25416, an environmental B. cepacia strain, do not bind to TNFR1 and stimulate only minimal IL-8 production from CF cells. Further, TNFR1 expression is increased in CF airway epithelial cells compared with non-CF cells. We also show that B. cenocepacia ET12 strain colocaizes with TNFR1 in vitro and in the lungs of CF patients who died due to infection with B. cenocepacia, ET12 strain. Together, these results suggest that interaction of B. cenocepacia, ET12 strain with TNFR1 may contribute to robust inflammatory responses elicited by this organism.

摘要

洋葱伯克霍尔德菌是囊性纤维化(CF)患者的一种重要肺部病原体。感染通常与严重的肺部炎症相关,一些患者会发展为致命的坏死性肺炎和败血症(“洋葱伯克霍尔德菌综合征”)。该菌种引发严重肺部炎症的机制尚不清楚。在此,我们证明了洋葱伯克霍尔德菌BC7,一种流行的ET12谱系的潜在致病代表菌株,可与肿瘤坏死因子受体1(TNFR1)结合,并激活与TNFR1相关的信号通路,类似于TNFR1的天然配体肿瘤坏死因子-α(TNF-α)。这种相互作用参与刺激CF气道上皮细胞产生大量白细胞介素-8(IL-8)。相比之下,毒性较低的ET12代表菌株BC45和环境菌株洋葱伯克霍尔德菌ATCC 25416不与TNFR1结合,仅刺激CF细胞产生极少的IL-8。此外,与非CF细胞相比,CF气道上皮细胞中TNFR1的表达增加。我们还表明,在体外以及死于洋葱伯克霍尔德菌ET12菌株感染的CF患者的肺中,洋葱伯克霍尔德菌ET12菌株与TNFR1共定位。总之,这些结果表明洋葱伯克霍尔德菌ET12菌株与TNFR1的相互作用可能导致该生物体引发强烈的炎症反应。

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