中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Reactivation of kaposi's sarcoma-associated herpesvirus from latency requires mek/erk, jnk and p38 multiple mitogen-activated protein kinase pathways

文献类型:期刊论文

作者Xie, Jianping1,2; Ajibade, Adetola Olalekan1,3; Ye, Fengchun1,2; Kuhne, Kurt1,3; Gao, Shou-Jiang1,2,3,4,5,6,7
刊名Virology
出版日期2008-02-05
卷号371期号:1页码:139-154
关键词Kaposi's sarcoma Kshv Reactivation Mapk pathways Ap-1 Rta Tpa
ISSN号0042-6822
DOI10.1016/j.virol.2007.09.040
通讯作者Gao, shou-jiang(gaos@uthscsa.edu)
英文摘要Lytic replication of kaposi's sarcoma-associated herpesvirus (kshv) promotes the progression of kaposi's sarcoma (ks), a dominant malignancy in patients with aids. while 12-o-tetradecanoyl-phorbol-13-acetate (tpa)-induced kshv reactivation from latency is mediated by the protein kinase c delta and mek/erk mitogen-activated protein kinase (mapk) pathways, we have recently shown that the mek/erk, jnk and p38 mapk pathways modulate kshv lytic replication during productive primary infection of human umbilical vein endothelial cells [pan, h., xie, j., ye, f., gao, s.j., 2006. modulation of kaposi's sarcoma-associated herpesvirus infection and replication by mek/erk, jnk, and p38 multiple mitogen-activated protein kinase pathways during primary infection. j. virol. 80 (11), 5371-5382]. here, we report that, besides the mek/erk pathway, the jnk and p38 mapk pathways also mediate tpa-induced kshv reactivation from latency. the mek/erk, jnk and p38 mapk pathways were constitutively activated in latent kshv-infected bcbl-1 cells. tpa treatment enhanced the levels of activated erk and p38 but not those of activated jnk. inhibitors of all three mapk pathways reduced tpa-induced production of kshv infectious virions in bcbl-1 cells in a dose-dependent fashion. the inhibitors blocked kshv lytic replication at the early stage(s) of reactivation, and reduced the expression of viral lytic genes including rta, a key immediate-early transactivator of viral lytic replication. activation of mapk pathways was necessary and sufficient for activating the promoter of rta. furthermore, we showed that the activation of rta promoter by mapk pathways was mediated by their downstream target ap-1. together, these findings suggest that mapk pathways might have general roles in regulating the life cycle of kshv by mediating both viral infection and switch from viral latency to lytic replication. (c) 2007 elsevier inc. all rights reserved.
WOS关键词NF-KAPPA-B ; NOTCH SIGNALING PATHWAY ; NUCLEAR ANTIGEN ; LYTIC REPLICATION ; PRIMARY INFECTION ; GENE-EXPRESSION ; C-JUN ; ENDOTHELIAL-CELLS ; INFLAMMATORY CYTOKINES ; RESPONSE ELEMENTS
WOS研究方向Virology
WOS类目Virology
语种英语
WOS记录号WOS:000252725700014
出版者ACADEMIC PRESS INC ELSEVIER SCIENCE
URI标识http://www.irgrid.ac.cn/handle/1471x/2375475
专题武汉病毒研究所
通讯作者Gao, Shou-Jiang
作者单位1.Univ Texas Hlth Sci Ctr San Antonio, Tumor Virol Program, Greehey Childrens Canc Res Inst, San Antonio, TX 78229 USA
2.Univ Texas Hlth Sci Ctr San Antonio, Dept Pediat, San Antonio, TX 78229 USA
3.Univ Texas Hlth Sci Ctr San Antonio, Dept Microbiol & Immunol, San Antonio, TX 78229 USA
4.Univ Texas Hlth Sci Ctr San Antonio, Dept Med, San Antonio, TX 78229 USA
5.Univ Texas Hlth Sci Ctr San Antonio, Dept Mol Med, San Antonio, TX 78229 USA
6.Univ Texas Hlth Sci Ctr San Antonio, San Antonio Canc Inst, San Antonio, TX 78229 USA
7.Chinese Acad Sci, Wuhan Inst Virol, Tumor Virol Grp, Wuhan, Peoples R China
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Xie, Jianping,Ajibade, Adetola Olalekan,Ye, Fengchun,et al. Reactivation of kaposi's sarcoma-associated herpesvirus from latency requires mek/erk, jnk and p38 multiple mitogen-activated protein kinase pathways[J]. Virology,2008,371(1):139-154.
APA Xie, Jianping,Ajibade, Adetola Olalekan,Ye, Fengchun,Kuhne, Kurt,&Gao, Shou-Jiang.(2008).Reactivation of kaposi's sarcoma-associated herpesvirus from latency requires mek/erk, jnk and p38 multiple mitogen-activated protein kinase pathways.Virology,371(1),139-154.
MLA Xie, Jianping,et al."Reactivation of kaposi's sarcoma-associated herpesvirus from latency requires mek/erk, jnk and p38 multiple mitogen-activated protein kinase pathways".Virology 371.1(2008):139-154.

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来源:武汉病毒研究所

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