Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/60882
Title: Sensitization to Fas-mediated apoptosis by dengue virus capsid protein
Authors: Thawornchai Limjindaporn
Janjuree Netsawang
Sansanee Noisakran
Somchai Thiemmeca
Wiyada Wongwiwat
Sangkab Sudsaward
Panisadee Avirutnan
Chunya Puttikhunt
Watchara Kasinrerk
Rungtawan Sriburi
Nopporn Sittisombut
Pa thai Yenchitsomanus
Prida Malasit
Authors: Thawornchai Limjindaporn
Janjuree Netsawang
Sansanee Noisakran
Somchai Thiemmeca
Wiyada Wongwiwat
Sangkab Sudsaward
Panisadee Avirutnan
Chunya Puttikhunt
Watchara Kasinrerk
Rungtawan Sriburi
Nopporn Sittisombut
Pa thai Yenchitsomanus
Prida Malasit
Keywords: Biochemistry, Genetics and Molecular Biology
Issue Date: 19-Oct-2007
Abstract: Dengue fever (DF) and dengue hemorrhagic fever (DHF) are important public health problems in tropical regions. Abnormal hemostasis and plasma leakage are the main patho-physiological changes in DHF. However, hepatomegaly, hepatocellular necrosis and fulminant hepatic failure are occasionally observed in patients with DHF. Dengue virus-infected liver cells undergo apoptosis but the underlying molecular mechanism remains unclear. Using a yeast two-hybrid screen, we found that dengue virus capsid protein (DENV C) physically interacts with the human death domain-associated protein Daxx, a Fas-associated protein. The interaction between DENV C and Daxx in dengue virus-infected liver cells was also demonstrated by co-immunoprecipitation and double immunofluorescence staining. The two proteins were predominantly co-localized in the cellular nuclei. Fas-mediated apoptotic activity in liver cells constitutively expressing DENV C was induced by anti-Fas antibody, indicating that the interaction of DENV C and Daxx involves in apoptosis of dengue virus-infected liver cells. © 2007 Elsevier Inc. All rights reserved.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=34548290826&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/60882
ISSN: 10902104
0006291X
Appears in Collections:CMUL: Journal Articles

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