IL-29 and IFN-α regulate the expression of MxA, 2',5'-OAS and PKR genes in association with the activation of Raf-MEK-ERK and PI3K-AKT signal pathways in HepG2.2.15 cells

被引:20
作者
Chai, Yu [1 ]
Huang, Hai-Liang [1 ]
Hu, Dao-Jun [1 ]
Luo, Xin [1 ]
Tao, Qian-Shan [1 ]
Zhang, Xiao-Ling [1 ]
Zhang, Sheng-Quan [1 ]
机构
[1] Anhui Med Univ, Dept Biochem & Mol Biol, Hefei 230032, Anhui, Peoples R China
关键词
Interleukin; 29; MxA; 2; 5; '-OAS; PKR; P-ERK; P-AKT; PROTEIN-KINASE; GROWTH-FACTOR; INTERFERON; GAMMA; RECEPTOR; INDUCTION; MECHANISM; CYTOKINES; MOUSE;
D O I
10.1007/s11033-010-0087-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Interferons (IFNs) can activate the PI3K-AKT and Raf-MEK-ERK signal pathways and induce antiviral proteins (MxA, 2',5'-OAS and PKR) expression in specific cell lines. However, the relationship between those antiviral proteins expression and signal pathways remains unknown at present. Thus our experiments were designed to determine the exact relationship in HepG2.2.15 cell line. The results demonstrated that IFN-alpha and IL-29 were both able to activate PI3K-AKT and Raf-MEK-ERK signal pathways, and IFN-alpha up-regulated the expression of MxA, 2',5'-OAS and PKR whereas IL-29 increased mRNA expression of MxA and 2',5'-OAS and had no influence on PKR. Furthermore, MxA, 2',5'-OAS and PKR expression were down-regulated while PI3K-AKT signal pathway was blocked by LY294002. And MxA was up-regulated after Raf-MEK-ERK signal pathway being blocked by PD98059. These findings indicate that the expression of MxA, 2',5'-OAS and PKR are up-regulate by PI3K-AKT signal pathway, and Raf-MEK-ERK signal pathway has a negative regulatory effect on the expression of MxA and no significant effect on 2',5'-OAS and PKR.
引用
收藏
页码:139 / 143
页数:5
相关论文
共 28 条
[1]   Interferons at age 50: past, current and future impact on biomedicine [J].
Borden, Ernest C. ;
Sen, Ganes C. ;
Uze, Gilles ;
Silverman, Robert H. ;
Ransohoff, Richard M. ;
Foster, Graham R. ;
Stark, George R. .
NATURE REVIEWS DRUG DISCOVERY, 2007, 6 (12) :975-990
[2]   The immune response modifier imiquimod requires STAT-1 for induction of interferon, interferon-stimulated genes, and interleukin-6 [J].
Bottrel, RLA ;
Yang, YL ;
Levy, DE ;
Tomai, M ;
Reis, LFL .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1999, 43 (04) :856-861
[3]   The haplotype of the MxA gene promoter is associated with hepatitis B virus infection in a Chinese population [J].
Cao, Bangwei ;
Liu, Xing ;
Hou, Fang ;
Li, Wende ;
Han, Zhonggang ;
Zhang, Qipeng ;
Dai, Yue ;
Xu, Changqing ;
Qi, Huimin .
LIVER INTERNATIONAL, 2009, 29 (09) :1383-1388
[4]   IFN-γ + LPS induction of iNOS is modulated by ERK, JNK/SAPK, and p38mapk in a mouse macrophage cell line [J].
Chan, ED ;
Riches, DWH .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2001, 280 (03) :C441-C450
[5]   Specificity and mechanism of action of some commonly used protein kinase inhibitors [J].
Davies, SP ;
Reddy, H ;
Caivano, M ;
Cohen, P .
BIOCHEMICAL JOURNAL, 2000, 351 (351) :95-105
[6]   A SYNTHETIC INHIBITOR OF THE MITOGEN-ACTIVATED PROTEIN-KINASE CASCADE [J].
DUDLEY, DT ;
PANG, L ;
DECKER, SJ ;
BRIDGES, AJ ;
SALTIEL, AR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (17) :7686-7689
[7]   Intracellular signalling and antiviral effects of interferons [J].
Heim, MH .
DIGESTIVE AND LIVER DISEASE, 2000, 32 (03) :257-263
[8]  
Hokeness K, 2005, ONCOL REP, V13, P965
[9]   The antiviral state induced by alpha interferon and gamma interferon requires transcriptionally active Stat1 protein [J].
Horvath, CM ;
Darnell, JE .
JOURNAL OF VIROLOGY, 1996, 70 (01) :647-650
[10]   Involvement of IL-1β and IL-10 in IFN-α-mediated antiviral gene induction in human hepatoma cells [J].
Ichikawa, T ;
Nakao, K ;
Nakata, K ;
Yamashita, M ;
Hamasaki, K ;
Shigeno, M ;
Abiru, S ;
Ishikawa, H ;
Ishii, N ;
Eguchi, K .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 294 (02) :414-422