Thromb Haemost 2010; 104(06): 1219-1227
DOI: 10.1160/TH10-05-0302
Wound Healing and Inflammation / Infection
Schattauer GmbH

The dengue virus envelope protein induced PAI-1 gene expression via MEK/ERK pathways

Huey-Wen Shyu
1   Department of Medical Technology, Fooyin University, Kaohsiung Hsien, Taiwan
,
Yi-Ying Lin
1   Department of Medical Technology, Fooyin University, Kaohsiung Hsien, Taiwan
2   5th Branch Office, Center for Disease Control, Kaohsiung, Taiwan
,
Lien-Cheng Chen
3   Bureau of Foods and Drug Analysis, Department of Health, Taiwan
,
Yi-Fen Wang
1   Department of Medical Technology, Fooyin University, Kaohsiung Hsien, Taiwan
,
Trai-Ming Yeh
4   Department of Medical Laboratory Sciences and Biotechnology, National Cheng Kung University, Tainan, Taiwan
,
Shu-Jem Su
1   Department of Medical Technology, Fooyin University, Kaohsiung Hsien, Taiwan
,
Wei-Cheng Cheng
5   Institute of Molecular Biology, Academia Sinica, Taipei, Taiwan
,
Chang-Yu Chen
1   Department of Medical Technology, Fooyin University, Kaohsiung Hsien, Taiwan
,
Kuan-Hua Lin
1   Department of Medical Technology, Fooyin University, Kaohsiung Hsien, Taiwan
,
Miao-Chen Chou
1   Department of Medical Technology, Fooyin University, Kaohsiung Hsien, Taiwan
› Author Affiliations
Further Information

Publication History

Received: 21 May 2010

Accepted after major revision: 15 August 2010

Publication Date:
24 November 2017 (online)

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Summary

Dengue virus (DV) infections cause mild dengue fever or severe life-threatening dengue haemorrhagic fever (DHF)/ dengue shock syndrome (DSS). DV-infected patients have high plasma concentrations of plasminogen activator inhibitor type I (PAI-1). However, the mechanism to cause haemorrhage in DV infections remains poorly understood. In this study, investigation was carried out on the purified recombinant domain III of the envelope glycoprotein of DV serotypes 2 (EIII) and the signalling pathways of EIII leading to PAI-1 gene expression were measured by RT-PCR, Western blot, and immunofluorescence stain. Reporter gene constructs containing serially 5’-deleted sequences of the proximal human PAI-1 promoter region were constructed and then transfected to Huh7 cells, a human hepatoma cell line, prior to EIII treatment. EIII increased the PAI-1 mRNA and protein levels in a dose-dependent manner in Huh7 cells. Results showed that U0126, an inhibitor of extracellular signal-regulated kinase (ERK) kinase (MEK), almost completely suppressed EIII-induced PAI-1 expression. The results suggest that the MEK/ERK signalling pathways mediate the EIII-dependent induction of PAI-1 gene expression via the proximal promoter region.