Rennoll-Bankert Kristen E, Sinclair Sara H, Lichay Marguerite A, Dumler J Stephen
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.
Pathog Dis. 2014 Jun;71(1):55-64. doi: 10.1111/2049-632X.12111. Epub 2013 Dec 20.
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.
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。