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由巴西紫癜热相关的埃及生物群流感嗜血杆菌菌株引起的人微血管内皮细胞毒性。

Human microvascular endothelial cell toxicity caused by Brazilian purpuric fever-associated strains of Haemophilus influenzae biogroup aegyptius.

作者信息

Weyant R S, Quinn F D, Utt E A, Worley M, George V G, Candal F J, Ades E W

机构信息

Emerging Bacterial and Mycotic Disease Branch, Centers for Disease Control and Prevention, Atlanta, Georgia 30333.

出版信息

J Infect Dis. 1994 Feb;169(2):430-3. doi: 10.1093/infdis/169.2.430.

Abstract

An in vitro cytotoxicity model that uses an immortalized human microvascular endothelial cell line (HMEC-1) differentiates Brazilian purpuric fever (BPF)-associated Haemophilus influenzae biogroup aegyptius (HAE) strains from non-BPF-associated HAE strains. Toxic strains produced a characteristic HMEC-1 phenotype at an MOI of < 1 bacterium/1000 tissue culture cells (TCC). Nontoxic strains required MOIs of > 1000 bacteria/TCC to produce an observable effect. The cytotoxic phenotype was characterized by the presence of large clumps of HMEC-1 cells, which detached from the monolayer within 48 h of inoculation by HAE cells. The cytotoxic phenotype was observed with 100% of BPF-associated HAE (40/40) and 14% of non-BPF-associated HAE (8/57; P < .001). The ability to study a BPF-associated phenotype in vitro using human microvascular cells should enhance our knowledge of BPF pathogenesis.

摘要

一种使用永生化人微血管内皮细胞系(HMEC-1)的体外细胞毒性模型,可将巴西紫癜热(BPF)相关的埃及嗜血杆菌生物群(HAE)菌株与非BPF相关的HAE菌株区分开来。毒性菌株在感染复数(MOI)<1个细菌/1000个组织培养细胞(TCC)时产生特征性的HMEC-1表型。无毒菌株需要MOI>1000个细菌/TCC才能产生可观察到的效应。细胞毒性表型的特征是存在大量HMEC-1细胞团块,这些细胞团块在HAE细胞接种后48小时内从单层中脱离。在100%的BPF相关HAE(40/40)和14%的非BPF相关HAE(8/57;P<.001)中观察到细胞毒性表型。利用人微血管细胞在体外研究BPF相关表型的能力应能增强我们对BPF发病机制的认识。

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