Differential proinflammatory and angiogenesis-specific cytokine production in human pulmonary endothelial cells, HPMEC-ST1.6R infected with dengue-2 and dengue-3 virus

被引:43
作者
Azizan, Azliyati
Sweat, James
Espino, Carlos
Gemmer, Jennifer
Stark, Lillian
Kazanis, Deno
机构
[1] Coll Publ Hlth, Global Hlth Dept, Tampa, FL 33612 USA
[2] Florida Dept Hlth, Bur Lab, Tampa, FL 33612 USA
[3] Florida Dept Hlth, Ctr Biol Def, Tampa, FL 33612 USA
关键词
dengue; microbead bioplex; dengue hemorrhagic fever; cytokines; endothelial cells; angiogenesis; HEMORRHAGIC-FEVER; SHOCK-SYNDROME; DNA VACCINE; GM-CSF; LINES; IMMUNOPATHOGENESIS; COAGULATION; ACTIVATION; EXPRESSION; CHALLENGE;
D O I
10.1016/j.jviromet.2006.08.010
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In this study, the ability of dengue virus serotypes 2 (DENV-2) and 3 (DENV-3) to infect and induce increased production of proinflammatory cytokines in a pulmonary endothelial cell line (HPMEC-ST1.6R) was investigated. This cell line exhibits the major constitutive and inducible endothelial cell characteristics, as well as angiogenic response. DENV-2 and DENV-3 infection was confirmed by an observed cytopathic effect (CPE), as well as RT-PCR and immunofluorescence assays. Increases in Th-1 and Th-2 cytokines IL-4, IL-8, IL-6, IL-10, GM-CSF, INF-gamma, and tumor necrosis factor (TNF-alpha) within DENV-2- and DENV-3-infected cells were demonstrated using a microbead-based Bio-plex assay. Proinflammatory cytokine increases and the expression of a potent angiogenic inducer protein, VEGF were confirmed by dot-blot analysis using the TranSignal (TM) Human Angiogenesis Antibody Array. Dengue virus-infected HPMEC-ST1.6R cells exhibited an elongated cytoplasmic morphology, possibly representing a response to VEGF and activation of angiogenesis. The increased levels of Th-1 cytokines and VEGF in DENV-2 virus infected-HPMEC-ST1.6R could be distinguished from those infected by DENV-3. This suggests that cytokine patterns associated with DENV infections may be serotype and strain-specific. The experimental approaches described here could be developed further into a useful diagnostic tool for the characterization of dengue hemorrhagic fever cases, leading to enhancement of treatment therapy. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:211 / 217
页数:7
相关论文
共 31 条
[1]   Systemic host inflammatory and coagulation response in the Dengue virus primo-infection [J].
Avila-Aguero, ML ;
Avila-Aguero, CR ;
Um, SL ;
Soriano-Fallas, A ;
Cañas-Coto, A ;
Yan, SB .
CYTOKINE, 2004, 27 (06) :173-179
[2]  
Avirutnan P, 1998, J IMMUNOL, V161, P6338
[3]   Increased production of interleukin-8 in primary human monocytes and in human epithelial and endothelial cell lines after dengue virus challenge [J].
Bosch, I ;
Xhaja, K ;
Estevez, L ;
Raines, G ;
Melichar, H ;
Warke, RV ;
Fournier, MV ;
Ennis, FA ;
Rothman, AL .
JOURNAL OF VIROLOGY, 2002, 76 (11) :5588-5597
[4]  
CHANDRASEKHAR B, 2003, JHEP, V306, P1
[5]   Simultaneous detection of 15 human cytokines in a single sample of stimulated peripheral blood mononuclear cells [J].
de Jager, W ;
te Velthuis, H ;
Prakken, BJ ;
Kuis, W ;
Rijkers, GT .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 2003, 10 (01) :133-139
[6]   TNF-α-308A allele, a possible severity risk factor of hemorrhagic manifestation in dengue fever patients [J].
Fernández-Mestre, MT ;
Gendzekhadze, K ;
Rivas-Vetencourt, P ;
Layrisse, Z .
TISSUE ANTIGENS, 2004, 64 (04) :469-472
[7]  
Gagnon Susan J., 2001, American Journal of Tropical Medicine and Hygiene, V64, P41
[8]   More Dengue, more questions [J].
Halstead, SB .
EMERGING INFECTIOUS DISEASES, 2005, 11 (05) :740-741
[9]   Dengue virus infects human endothelial cells and induces IL-6 and IL-8 production [J].
Huang, YH ;
Lei, HY ;
Liu, HS ;
Lin, YS ;
Liu, CC ;
Yeh, TM .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 2000, 63 (1-2) :71-75
[10]   Dengue hemorrhagic fever in infants: A study of clinical and cytokine profiles [J].
Hung, NT ;
Lei, HY ;
Lan, NT ;
Lin, YS ;
Huang, KJ ;
Lien, LB ;
Lin, CF ;
Yeh, TM ;
Ha, DQ ;
Huong, VTQ ;
Chen, LC ;
Huang, JH ;
My, LT ;
Liu, CC ;
Halstead, SB .
JOURNAL OF INFECTIOUS DISEASES, 2004, 189 (02) :221-232