Upregulation of Nrf2 expression by human cytomegalovirus infection protects host cells from oxidative stress

被引:42
作者
Lee, Junsub [1 ]
Koh, Kyungmi [1 ]
Kim, Young-Eui [2 ]
Ahn, Jin-Hyun [2 ]
Kim, Sunyoung [1 ]
机构
[1] Seoul Natl Univ, Sch Biol Sci, Seoul 151747, South Korea
[2] Sungkyunkwan Univ, Sch Med, Samsung Biomed Res Inst, Dept Mol Cell Biol, Suwon 440746, Kyonggido, South Korea
基金
新加坡国家研究基金会;
关键词
ACTIVATION; REPLICATION; DISEASE; RISK; ACCUMULATION; FAMILY; GROWTH; GENES; DNA; CK2;
D O I
10.1099/vir.0.052142-0
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
NF-E2 related factor 2 (Nrf2) is a transcription factor that plays a key role(s) in cellular defence against oxidative stress. In this study, we showed that the expression of Nrf2 was upregulated in primary human foreskin fibroblasts (HFFs), following human cytomegalovirus (HCMV/HHV-5) infection. The expression of haem oxygenase-1, a downstream target of Nrf2, was also increased by HCMV infection, and this induction was suppressed in HFFs expressing a small hairpin RNA (shRNA) against Nrf2. The HCMV-mediated increase in Nrf2 expression was abolished when UV-irradiated virus was used or when the activity of casein kinase 2 was inhibited. Host cells infected by HCMV had higher survival rates following oxidative stress induced by buthionine sulfoximine compared with uninfected control cells, but this cell-protective effect was abolished by the use of Nrf2 shRNA. Our results suggest that HCMV-mediated activation of Nrf2 might be beneficial to the virus by increasing the host cell's ability to cope with oxidative stress resulting from viral infection and/or inflammation.
引用
收藏
页码:1658 / 1668
页数:11
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