Modulation of NB4 promyelocytic leukemic cell machinery by Anaplasma phagocytophilum

被引:31
作者
Pedra, JHF
Sukumaran, B
Carlyon, JA
Berliner, N
Fikrig, E
机构
[1] Yale Univ, Sch Med, Dept Internal Med, Rheumatol Sect,Anlyan Ctr Med Res & Educ, New Haven, CT 06520 USA
[2] Univ Kentucky, Coll Med, Dept Microbiol Immunol & Mol Genet, Lexington, KY USA
[3] Yale Univ, Sch Med, Dept Internal Med, Sect Hematol, New Haven, CT USA
基金
美国国家卫生研究院;
关键词
NB4; Anaplasma phagocytophilum; Ehrlichia spp; microarray; 2D-DIGE;
D O I
10.1016/j.ygeno.2005.05.008
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Anaplasma phagocytophilum is a gram-negative obligate intracellular bacterium that persists within neutropbils. We assessed the impact of A. phagoevtophilum infection in NB4 promyelocytic leukemic cells using high-density oligoarray, two-dimensional differential gel electrophoresis and liquid chromatography-mass spectrometry. Our Affymetrix data revealed that A. phagocytophilum altered the expression of transcription factors, cell adhesion molecules, signal transduction genes, and proinflammatory cytokines. However, the expression of Toll-like receptors, MYD88, RNF36, IRF3, and TBK1 and inhibitors of the NF-kappa B gene was not altered. A. phagocytophilum infection also altered the apoptotic program of NB4 cells and resulted in increased transcription of antiapoptotic genes (MCL1 and BFL1). The transcription and translation of iron-metabolism genes (light polypeptide ferritin chain, transferrin, and the transferrin receptor) were significantly altered, suggesting a possible link between A. phagocytophilum infection and iron metabolism. Our study clearly demonstrates multifactorial effects of A. phagocytophilum infection on NB4 promyelocytic leukemic cell machinery. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:365 / 377
页数:13
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