Senescence affects endothelial cells susceptibility to dengue virus infection

International Journal of Medical Sciences

Volumn 11, Issue 6, 2014, Pages 538-544

  Abubakar, Sazaly ^a   Shu, Meng Hooi ^a   Johari, Jefree ^a   Wong, Pooi Fong ^a  

^a UNIVERSITY OF MALAYA   (Malaysia)

Author keywords

Dengue virus; Endothelial cells; Endothelium permeability; HUVECs; Senescence

Indexed keywords

VIRUS RNA;

AEDES ALBOPICTUS; ANIMAL CELL; ARTICLE; CELL COUNTING; CELL CYCLE ARREST; CELL MEMBRANE PERMEABILITY; CELL STRUCTURE; CONTROLLED STUDY; DENGUE; DENGUE VIRUS 2; DNA CONTENT; FOCI FORMING UNIT; G2 PHASE CELL CYCLE CHECKPOINT; GENE DOSAGE; HUMAN; HUMAN CELL; INFECTION SENSITIVITY; NONHUMAN; SENESCENCE; UMBILICAL VEIN ENDOTHELIAL CELL; CELL AGING; DENGUE VIRUS; ENDOTHELIUM CELL; GENETICS; PATHOGENICITY; VIROLOGY;

CELL AGING; CELL MEMBRANE PERMEABILITY; DENGUE; DENGUE VIRUS; ENDOTHELIAL CELLS; HUMAN UMBILICAL VEIN ENDOTHELIAL CELLS; HUMANS; SEVERE DENGUE;

EID: 84898420796     PISSN: 14491907     EISSN: None     Source Type: Journal    
DOI: 10.7150/ijms.7896     Document Type: Article

References (37)

1. AbuBakar S, Wong PF, Chan YF. Emergence of dengue virus type 4 genotype IIA in Malaysia. Journal of General Virology. 2002; 83: 2437-2442.
2. Shafee N, AbuBakar S. Dengue virus type 2 NS3 protease and NS2B-NS3 protease precursor induce apoptosis. Journal of General Virology. 2003; 84:2191-2195.
3. Nathan MB, Dayal-Drager R. Recent epidemiological trends, the global strategy and public health advances in dengue. Report on Dengue. 2006;: 30-34.
4. [Internet] World Health Organization. Dengue and severe dengue. http://www.who.int/mediacentre/factsheets/fs117/en/index.html.
5. [Internet] World Health Organization. Global strategy for dengue prevention and control 2012-2020. http://apps.who.int/iris/bitstream/10665/75303/1/9789241504034_eng.pdf.
6. World Health Organization Regional Office for South-East Asia. Comprehensive guidelines for prevention and control of dengue and dengue haemorrhagic fever. World Health Organization. 2011.
7. Special Programme for Research, Training in Tropical Diseases, World Health Organization; Department of Control of Neglected Tropical Diseases, World Health Organization; Department of Epidemic and Pandemic Alert. Dengue: guidelines for diagnosis, treatment, prevention and control. World Health Organization. 2009.
8. Liu P, Woda M, Ennis FA, et al. Dengue virus infection differentially regulates endothelial barrier function over time through type I interferon effects. The Journal of Infectious Diseases. 2009; 200: 191-201.
9. Srichaikul T, Nimmannitya S. Haematology in dengue and dengue haemorrhagic fever. Baillière's Clinical Haematology. 2000; 13(2): 261-276.
10. Lei HY, Huang KJ, Lin YS, et al. Immunopathogenesis of dengue hemorrhagic fever. American Journal of Infectious Diseases. 2008; 4(1): 1-9.
11. Basu A, Chaturvedi UC. Vascular endothelium: the battlefield of dengue viruses. FEMS Immunology and Medical Microbiology. 2008; 53: 287-299.
12. Srikiatkhachorn A. Plasma leakage in dengue haemorrhagic fever. Thrombosis and Haemostasis. 2009; 102(6): 1042-1049.
13. Noisakran S, Onlamoon N, Songprakhon P, et al. Cells in dengue virus infection in vivo. Advances in Virology. 2010.
14. McBride WJH, Bielefeldt-Ohmann H. Dengue viral infections: pathogenesis and epidemiology. Microbes and Infection. 2000; 2(9): 1041-1050.
15. Dalrymple NA, Mackow ER. Endothelial cells elicit immune-enhancing responses to dengue virus infection. Joural of Virology. 2012; 86(12): 6408-6415.
16. Mota J, Rico-Hesse R. Dengue virus tropism in humanized mice recapitulates human dengue fever. Plos One. 2011; 6(6): e20762.
17. Kyle JL, Beatty PR, Harris E. Dengue virus infects macrophages and dendritic cells in a mouse model of infection. The Journal of Infectious Diseases. 2007; 195: 1808-1817.
18. Warke RV, Xhaja K, Martin KJ, et al. Dengue virus induces novel changes in gene expression of human umbilical vein endothelial cells. Journal of Virology. 2003; 77(21): 11822-11832.
19. Avirutnan P, Malasit P, Seliger B, et al. Dengue virus infection of human endothelial cells leads to chemokine production, complement activation and apoptosis. The Journal of Immunology. 1998; 161: 6338-6346.
20. Appanna R, Wang SM, Ponnampalavanar SA, et al. Cytokine factors present in dengue patient sera induces alterations of junctional proteins in human endothelial cells. The American Journal of Tropical Medicine and Hygiene. 2012; 87(5): 936-942.
21. Limonta D, Capó V, Torres G, et al. Apoptosis in tissues from fatal dengue shock syndrome. Journal of Clinical Virology. 2007; 40: 50-54.
22. Krouwer VJD, Hekking LHP, Langelaar-Makkinje M, et al. Endothelial cell senescence is associated with disrupted cell-cell junctions and increased monolayer permeability. Vascular Cell. 2012; 4(12): 1-10.
23. Azeredo EL, Oliveira-Pinto LMD, Zagne SM, et al. NK cells, displaying early activation, cytotoxicity and adhesion molecules, are associated with mild dengue disease. Clinical and Experimental Immunology. 2006; 143(2): 345-356.
24. Nightingale ZD, Patkar C, Rothman AL. Viral replication and paracrine effects result in distinct, functional responses of dendritic cells following infection with dengue 2 virus. Journal of Leukocyte Biology. 2008; 84(4): 1028-1038.
25. Van der Loo B, Fenton MJ, Erusalimsky JD. Cytochemical detection of a senescence-associated β-galactosidase in endothelial and smooth muscle cells from human and rabbit blood vessels. Experimental Cell Research. 1998; 241:309-315.
26. Okuno Y, Fukunaga T, Srisupaluck S, et al. A modified PAP (peroxidase-anti-peroxidase) staining technique using sera from patients with dengue hemorrhagic fever (DHF): 4 step PAP staining technique. Biken Journal. 1979; 22(4): 131-135.
27. Zandi K, Teoh BT, Sam SS, et al. In vitro antiviral activity of Fisetin, Rutin and Naringenin against dengue virus type-2. Journal of Medicinal Plants Research. 2011; 5(23): 5534-5539.
28. Wagner M, Hampel B, Bernhard D, et al. Replicative senescence of human endothelial cells in vitro involves G1 arrest, polyploidization and senescence-associated apoptosis. Experimental Gerontology. 2001; 36: 1327-1347.
29. Lee ST, Wong PF, Cheah SC, et al. Alpha-tomatine induces apoptosis and inhibits nuclear factor-kappa B activation on human prostatic adenocarcinoma PC-3 cells. Plos One. 2011; 6(4): e18915
30. Solly K, Wang X, Xu X, et al. Application of Real-Time Cell Electronic Sensing (RT-CES) technology to cell-based assays. Assay and Drug Development Technologies. 2004; 2(4): 363-372.
31. Huang YH, Lei HY, Liu HS, et al. Dengue virus infects human endothelial cells and induces IL-6 and IL-8 production. The American Journal of Tropical Medicine and Hygiene. 2000; 63: 71-75.
32. Huang YH, Lei HY, Liu HS, et al. Tissue plasminogen activator induced by dengue virus infection of human endothelial cells. Journal of Medical Virology. 2003; 70: 610-616.
33. Dalrymple N, Mackow ER. Productive dengue virus infection of human endothelial cells is directed by heparan sulfate-containing proteoglycan receptors. Journal of Virology. 2011; 85(18): 9478-9485.
34. Jacobs M, Levin M. An improved endothelial barrier model to investigate dengue haemorrhagic fever. Journal of Virological Methods. 2002; 104: 173-185.
35. Dewi BE, Takasaki T, Kurane I. Peripheral blood mononuclear cells increase the permeability of dengue virus-infected endothelial cells in association with downregulation of vascular endothelial cadherin. Journal of General Virology. 2008; 89: 642-652.
36. Heo JI, Cho JH, Kim JR. HJURP regulates cellular senescence in human fibroblasts and endothelial cells via a p53-dependent pathway. The Journals of Gerontology Series A: Biological Sciences and Medical Sciences. 2013.
37. Dimri GP, Lee XH, Basile G, et al. A biomarker that identifies senescent human cells in culture and in aging skin in vivo. Proceedings of the National Academy Sciences of the United States of America. 1995; 92: 9363-9367.