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Dexamethasone-induced cytokine changes associated with diminished disease severity in horses infected with Anaplasma phagocytophilum.地塞米松诱导的细胞因子变化与感染嗜吞噬细胞无形体的马匹疾病严重程度减轻相关。
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Epigenetic silencing of host cell defense genes enhances intracellular survival of the rickettsial pathogen Anaplasma phagocytophilum.宿主细胞防御基因的表观遗传沉默增强了立克次氏体病原体嗜吞噬细胞无形体的细胞内存活能力。
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Silencing of host cell CYBB gene expression by the nuclear effector AnkA of the intracellular pathogen Anaplasma phagocytophilum.细胞内病原体嗜吞噬细胞无形体的核效应蛋白AnkA对宿主细胞CYBB基因表达的沉默作用。
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Anaplasma phagocytophilum-induced gene expression in both human neutrophils and HL-60 cells.嗜吞噬细胞无形体诱导人中性粒细胞和HL-60细胞中的基因表达。
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Anaplasma phagocytophilum AnkA secreted by type IV secretion system is tyrosine phosphorylated by Abl-1 to facilitate infection.嗜吞噬细胞无形体通过IV型分泌系统分泌的AnkA被Abl-1酪氨酸磷酸化以促进感染。
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Differential innate immune cell activation and proinflammatory response in Anaplasma phagocytophilum infection.嗜吞噬细胞无形体感染中先天性免疫细胞的差异性激活及促炎反应
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Transformation of Anaplasma phagocytophilum.嗜吞噬细胞无形体的转化
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Anaplasma phagocytophilum delays spontaneous human neutrophil apoptosis by modulation of multiple apoptotic pathways.嗜吞噬细胞无形体通过调节多种凋亡途径延迟人中性粒细胞的自发凋亡。
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Anaplasma phagocytophilum causes global induction of antiapoptosis in human neutrophils.嗜吞噬细胞无形体可引起人类中性粒细胞抗凋亡的整体诱导。
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嗜吞噬细胞无形体感染的粒细胞细胞模型的比较与表征

Comparison and characterization of granulocyte cell models for Anaplasma phagocytophilum infection.

作者信息

Rennoll-Bankert Kristen E, Sinclair Sara H, Lichay Marguerite A, Dumler J Stephen

机构信息

Department of Microbiology and Immunology, University of Maryland School of Medicine, Baltimore, MD, USA; Division of Medical Microbiology, Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.

出版信息

Pathog Dis. 2014 Jun;71(1):55-64. doi: 10.1111/2049-632X.12111. Epub 2013 Dec 20.

DOI:10.1111/2049-632X.12111
PMID:24376092
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4037391/
Abstract

Anaplasma phagocytophilum, an obligate intracellular bacterium, modifies functions of its in vivo host, the neutrophil. The challenges of using neutrophils ex vivo necessitate cell line models. However, cell line infections do not currently mimic ex vivo neutrophil infection characteristics. To understand these discrepancies, we compared infection of cell lines to ex vivo human neutrophils and differentiated hematopoietic stem cells with regard to infection capacity, oxidative burst, host defense gene expression, and differentiation. Using established methods, marked ex vivo neutrophil infection heterogeneity was observed at 24-48 h necessitating cell sorting to obtain homogeneously infected cells at levels observed in vivo. Moreover, gene expression of infected cell lines differed markedly from the prior standard of unsorted infected neutrophils. Differentiated HL-60 cells sustained similar infection levels to neutrophils in vivo and closely mimicked functional and transcriptional changes of sorted infected neutrophils. Thus, care must be exercised using ex vivo neutrophils for A. phagocytophilum infection studies because a major determinant of transcriptional and functional changes among all cells was the intracellular bacteria quantity. Furthermore, comparisons of ex vivo neutrophils and the surrogate HL-60 cell model allowed the determination that specific cellular functions and transcriptional programs are targeted by the bacterium without significantly modifying differentiation.

摘要

嗜吞噬细胞无形体是一种专性细胞内细菌,它会改变其体内宿主中性粒细胞的功能。在体外使用中性粒细胞存在诸多挑战,因此需要细胞系模型。然而,目前细胞系感染并不能模拟体外中性粒细胞感染的特征。为了理解这些差异,我们比较了细胞系感染与体外人中性粒细胞以及分化造血干细胞在感染能力、氧化爆发、宿主防御基因表达和分化方面的情况。使用既定方法,在24至48小时观察到显著的体外中性粒细胞感染异质性,这就需要进行细胞分选以获得体内观察到的水平的均匀感染细胞。此外,感染细胞系的基因表达与未分选的感染中性粒细胞的先前标准有显著差异。分化的HL - 60细胞在体内维持与中性粒细胞相似的感染水平,并紧密模拟分选的感染中性粒细胞的功能和转录变化。因此,在使用体外中性粒细胞进行嗜吞噬细胞无形体感染研究时必须谨慎,因为所有细胞中转录和功能变化的一个主要决定因素是细胞内细菌数量。此外,对体外中性粒细胞和替代HL - 60细胞模型的比较表明,该细菌靶向特定的细胞功能和转录程序,而不会显著改变分化。