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Identification of gene expression profiles in HeLa cells and HepG2 cells infected with Coxsackievirus B3
被引:8
|作者:
Rassmann, Alexander
[2
,3
,5
]
Martin, Ulrike
[1
]
Saluz, Hans-Peter
[2
,3
]
Peter, Stefan
[4
]
Munder, Thomas
[2
,3
,6
]
Henke, Andreas
[1
]
机构:
[1] Univ Jena, Jena Univ Hosp, Dept Virol & Antiviral Therapy, D-07745 Jena, Germany
[2] Leibniz Inst Nat Prod Res, Jena, Germany
[3] Infect Biol Hans Knoll Inst, Dept Cell & Mol Biol, Jena, Germany
[4] HELIOS Clin Ctr Erfurt, Dept Children & Youth Med, Erfurt, Germany
[5] Med Diagnostik GmbH, Biosci Inst, Gotha, Germany
[6] Univ Appl Sci Jena, Dept Med Engn & Biotechnol, Jena, Germany
关键词:
Coxsackievirus B3;
DNA microarray;
Expression profile;
PAN-CASPASE INHIBITORS;
FACTOR RECEPTOR FAMILY;
CAPSID PROTEIN VP2;
GROWTH-FACTOR;
B3-INDUCED MYOCARDITIS;
PROAPOPTOTIC PROTEIN;
APOPTOSIS;
ACTIVATION;
VIRUSES;
PATHWAY;
D O I:
10.1016/j.jviromet.2012.08.025
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
Viral infections of host cells cause multiple changes of cellular metabolism including immediate defense mechanisms as well as processes to support viral replication. Coxsackievirus B3 (CVB3) is a member of the Picornavirus family and is responsible for a wide variety of mild or severe infections including acute and chronic inflammations. Thereby, intracellular signaling can be changed very comprehensively. In order to compare the influence of CVB3 replication on gene expression pattern of two different cell lines. DNA microarray systems were used to study a set of 780 genes related to inflammation. Expression analysis of HeLa cells and HepG2 cells infected with CVB3 identified 34 genes whose mRNA levels were altered significantly upon infection. The expression of additional 16 genes in HepG2 cells and 31 genes in HeLa cells were found to be influenced during CVB3 replication as well. All genes expressed differentially were sorted with regard to their functions and interpreted in view of known contributors to the infection process. The activation of the tumor necrosis factor pathways by CVB3 represents one peculiar observation, including apoptosis, stress, and inflammation responses. (C) 2012 Elsevier B.V. All rights reserved.
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页码:190 / 194
页数:5
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