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.
引用
收藏
页码:190 / 194
页数:5
相关论文
共 50 条
  • [31] Identification of differentially expressed genes (DEGs) by malachite green in HepG2 cells
    Kim, Youn-Jung
    Song, Mee
    Ryu, Jae-Chun
    MOLECULAR & CELLULAR TOXICOLOGY, 2008, 4 (01) : 22 - 30
  • [32] Gene expression and integrated stress response in HepG2/C3A cells cultured in amino acid deficient medium
    Sikalidis, Angelos K.
    Lee, Jeong-In
    Stipanuk, Martha H.
    AMINO ACIDS, 2011, 41 (01) : 159 - 171
  • [33] Proteomic identification of proteins involved in the anticancer activities of oridonin in HepG2 cells
    Wang, Hui
    Ye, Yan
    Pan, Si-Yuan
    Zhu, Guo-Yuan
    Li, Ying-Wei
    Fong, David W. F.
    Yu, Zhi-Ling
    PHYTOMEDICINE, 2011, 18 (2-3) : 163 - 169
  • [34] RIP3 Regulates Autophagy and Promotes Coxsackievirus B3 Infection of Intestinal Epithelial Cells
    Harris, Katharine G.
    Morosky, Stefanie A.
    Drummond, Coyne G.
    Patel, Maulik
    Kim, Chonsaeng
    Stolz, Donna B.
    Bergelson, Jeffrey M.
    Cherry, Sara
    Coyne, Carolyn B.
    CELL HOST & MICROBE, 2015, 18 (02) : 221 - 232
  • [35] Interleukin-8 in HepG2 cells: Enhancing antiviral proteins in uninfected cells but promoting HBV replication in infected cells
    Yang, Kai
    Zhu, Yukai
    Chen, Jin
    Zhou, Weifeng
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2024, 734
  • [37] Silencing of Human CutC Gene (hCutC) Induces Apoptosis in HepG2 Cells
    Remesh Kunjunni
    Sandeep Sathianathan
    Madhuri Behari
    Parthaprasad Chattopadhyay
    Vivekanandhan Subbiah
    Biological Trace Element Research, 2016, 172 : 120 - 126
  • [38] Silencing of Human CutC Gene (hCutC) Induces Apoptosis in HepG2 Cells
    Kunjunni, Remesh
    Sathianathan, Sandeep
    Behari, Madhuri
    Chattopadhyay, Parthaprasad
    Subbiah, Vivekanandhan
    BIOLOGICAL TRACE ELEMENT RESEARCH, 2016, 172 (01) : 120 - 126
  • [39] Changes of miRNA and mRNA expression in HepG2 cells treated by epigallocatechin gallate
    Ahn, Joon-Ik
    Jeong, Kyung Ji
    Ko, Moon-Jeong
    Shin, Hee Jung
    Kim, Hye Soo
    Chung, Hye Joo
    Jeong, Ho-Sang
    MOLECULAR & CELLULAR TOXICOLOGY, 2010, 6 (02) : 169 - 177
  • [40] Hepatitis C virus protein expression induces apoptosis in HepG2 cells
    Kalkeri, G
    Khalap, N
    Garry, RF
    Fermin, CD
    Dash, S
    VIROLOGY, 2001, 282 (01) : 26 - 37