Measles virus induces cell-type specific changes in gene expression

被引:28
作者
Sato, Hiroki [1 ]
Honma, Reiko [2 ]
Yoneda, Misako [1 ]
Miura, Ryuichi [1 ]
Tsukiyama-Kohara, Kyoko [3 ]
Ikeda, Fusako [1 ]
Seki, Takahiro [1 ]
Watanabe, Shinya [2 ]
Kai, Chieko [1 ]
机构
[1] Univ Tokyo, Inst Med Sci, Lab Anim Res Ctr, Minato Ku, Tokyo 1088639, Japan
[2] Tokyo Med & Dent Univ, Bunkyo Ku, Tokyo, Japan
[3] Kumamoto Univ, Fac Med & Pharmaceut Sci, Kumamoto, Kumamoto, Japan
关键词
measles virus; Microarray; v protein; IFN signaling; lymphoid cells; epithelial cells;
D O I
10.1016/j.virol.2008.02.015
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Measles virus (MV) causes various responses including the induction of immune responses, transient immunosuppression and establishment of long-lasting immunity. To obtain a comprehensive view of the effects of MV infection on target cells, DNA microarray analyses of two different cell-types were performed. An epithelial (293SLAM; a 293 cell line stably expressing SLAM) and lymphoid (COBL-a) cell line were inoculated with purified wild-type MV. Microarray analyses revealed significant differences in the regulation of cellular gene expression between these two different cells. In 293 SLAM cells, upregulation of genes involved in the antiviral response was rapidly induced; in the later stages of infection, this was followed by regulation of many genes across a broad range of functional categories. On the other hand, in COBL-a cells, only a limited set of gene expression profiles was modulated after MV infection. Since it was reported that V protein of MV inhibited the IFN signaling pathway, we performed a microarray analysis using V knockout MV to evaluate V protein's effect on cellular gene expression. The V knockout MV displayed a similar profile to that of parental MV. In particular, in COBL-a cells infected with the virus, no alteration of cellular gene expression, including IFN signaling, was observed. Furthermore, IFN signaling analyzed in vitro was completely suppressed by MV infection in the COBL-a cells. These results reveal that MV induces different cellular responses in a cell-type specific manner. Microarray analyses will provide us useful information about potential mechanisms of MV pathogenesis. (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:321 / 330
页数:10
相关论文
共 39 条
[1]   Measles virus-induced modulation of host-cell gene expression [J].
Bolt, G ;
Berg, K ;
Blixenkrone-Moller, M .
JOURNAL OF GENERAL VIROLOGY, 2002, 83 :1157-1165
[2]  
DHIBJALBUT SS, 1993, J IMMUNOL, V151, P6248
[3]   The host response to West Nile Virus infection limits viral spread through the activation of the interferon regulatory factor 3 pathway [J].
Fredericksen, BL ;
Smith, M ;
Katze, MG ;
Shi, PY ;
Gale, M .
JOURNAL OF VIROLOGY, 2004, 78 (14) :7737-7747
[4]   The interferon antiviral response: from viral invasion to evasion [J].
Grandvaux, N ;
tenOever, BR ;
Servant, MJ ;
Hiscott, J .
CURRENT OPINION IN INFECTIOUS DISEASES, 2002, 15 (03) :259-267
[5]   Transcriptional profiling of interferon regulatory factor 3 target genes: Direct involvement in the regulation of interferon-stimulated genes [J].
Grandvaux, N ;
Servant, MJ ;
tenOever, B ;
Sen, GC ;
Balachandran, S ;
Barber, GN ;
Lin, RT ;
Hiscott, J .
JOURNAL OF VIROLOGY, 2002, 76 (11) :5532-5539
[6]  
Griffin DE, 2001, MEASLES VIRUS FIELDS, P1401
[7]   Measles virus enhances the expression of cellular immediate-early genes and DNA-binding of transcription factor AP-1 in lung epithelial A549 cells [J].
Helin, E ;
Matikainen, S ;
Julkunen, L ;
Heino, J ;
Hyypiä, T ;
Vainionpää, R .
ARCHIVES OF VIROLOGY, 2002, 147 (09) :1721-1732
[8]   Measles virus activates NF-κB and STAT transcription factors and production of IFN-α/β and IL-6 in the human lung epithelial cell line A549 [J].
Helin, E ;
Vainionpää, R ;
Hyypiä, T ;
Julkunen, I ;
Matikainen, S .
VIROLOGY, 2001, 290 (01) :1-10
[9]   A tetraspanin-family protein, T-Cell acute lymphoblastic leukemia-associated antigen 1, is induced by the Ewing's sarcoma-Wilms' tumor 1 fusion protein of desmoplastic small round-cell tumor [J].
Ito, E ;
Honma, R ;
Imai, J ;
Azuma, S ;
Kanno, T ;
Mori, S ;
Yoshie, O ;
Nishio, J ;
Iwasaki, H ;
Yoshida, K ;
Gohda, J ;
Inoue, J ;
Watanabe, S ;
Semba, K .
AMERICAN JOURNAL OF PATHOLOGY, 2003, 163 (06) :2165-2172
[10]   Dynamic regulation of gene expression by the Flt-1 kinase and Matrigel in endothelial tubulogenesis [J].
Kobayashi, S ;
Ito, E ;
Honma, R ;
Nojima, Y ;
Shibuya, M ;
Watanabe, S ;
Maru, Y .
GENOMICS, 2004, 84 (01) :185-192