败血症
肺
生物
下调和上调
免疫学
内皮
TLR4型
菌血症
先天免疫系统
整合素αM
微生物学
炎症
免疫系统
医学
抗生素
基因
内分泌学
内科学
生物化学
作者
Bryan G. Yipp,Jung Hwan Kim,Ronald Lima,Lori Zbytnuik,Björn Petri,Nick Swanlund,May Ho,Vivian G. Szeto,Tamar Tak,Leo Koenderman,Peter Pickkers,Anton T. J. Tool,Taco W. Kuijpers,Timo K. van den Berg,Mark R. Looney,Matthew F. Krummel,Paul Kubes
出处
期刊:Science immunology
[American Association for the Advancement of Science]
日期:2017-04-21
卷期号:2 (10)
被引量:190
标识
DOI:10.1126/sciimmunol.aam8929
摘要
Bloodstream infection is a hallmark of sepsis, a medically emergent condition requiring rapid treatment. However, upregulation of host defense proteins through toll-like receptors and NFκB requires hours after endotoxin detection. Using confocal pulmonary intravital microscopy, we identified that the lung provides a TLR4-Myd88-and abl tyrosine kinase-dependent niche for immediate CD11b-dependent neutrophil responses to endotoxin and Gram-negative bloodstream pathogens. In an in vivo model of bacteremia, neutrophils crawled to and rapidly phagocytosed Escherichia coli sequestered to the lung endothelium. Therefore, the lung capillaries provide a vascular defensive niche whereby endothelium and neutrophils cooperate for immediate detection and capture of disseminating pathogens.
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