IFI6 Inhibits Apoptosis via Mitochondrial-Dependent Pathway in Dengue Virus 2 Infected Vascular Endothelial Cells
Dengue hemorrhagic fever (DHF)/Dengue shock syndrome (DSS) is a fatal infectious disease that demands an effective treatment. Interferon (IFN)-stimulated genes (ISGs) induced by dengue virus (DENV) exert antiviral effects. Among ISGs, IFN-α inducible gene 6 (IFI6) was increased in DENV infected huma...
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Published in | PloS one Vol. 10; no. 8; p. e0132743 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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Abstract | Dengue hemorrhagic fever (DHF)/Dengue shock syndrome (DSS) is a fatal infectious disease that demands an effective treatment. Interferon (IFN)-stimulated genes (ISGs) induced by dengue virus (DENV) exert antiviral effects. Among ISGs, IFN-α inducible gene 6 (IFI6) was increased in DENV infected human umbilical vascular endothelial cells (HUVECs) by microarray analysis in our previous study. However, its function is incompletely understood. In this study, we confirmed that IFI6 was markedly induced in DENV infection of both primary HUVECs and EA.hy926 cell lines. Recombinant EA.hy926 cell lines in which IFI6 was either over-expressed (IFI6+/+) or knocked-down (IFI6-/-) were generated. The activation of caspase-3 and intrinsic apoptosis-related protein caspase-9 were down-regulated in IFI6+/+ but up-regulated in IFI6-/- cells at 24-48 hrs post-infection. After incubation with DENV for 48 hrs, the mitochondrial membrane potential (Δψ(m)) was more stable in IFI6+/+ cells but reduced in IFI6-/- cells, as assayed by fluorescence staining with JC-1. We observed that Bcl-2 expression was increased in IFI6+/+ and decreased in IFI6-/- cells. By contrast, Bax expression was decreased in IFI6+/+ and increased in IFI6-/- cells. It is presumed that the anti-apoptotic function of IFI6 is expressed by regulating the rheostatic balance between bcl-2/bax expression and inhibition of Δψ(m) depolarization during DENV infection of vascular endothelial cells(VECs). In addition, the pro-apoptotic protein X-linked Inhibitor of Apoptosis (XIAP)-Associated Factor 1(XAF1) expression had been reported to be up-regulated and led to the induction of apoptosis in DENV2-infected VECs,but the relationship between XAF1 and IFI6 dengue virus-induced apoptosis in VECs warrants further study. |
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AbstractList | Dengue hemorrhagic fever (DHF)/Dengue shock syndrome (DSS) is a fatal infectious disease that demands an effective treatment. Interferon (IFN)-stimulated genes (ISGs) induced by dengue virus (DENV) exert antiviral effects. Among ISGs, IFN-α inducible gene 6 (IFI6) was increased in DENV infected human umbilical vascular endothelial cells (HUVECs) by microarray analysis in our previous study. However, its function is incompletely understood. In this study, we confirmed that IFI6 was markedly induced in DENV infection of both primary HUVECs and EA.hy926 cell lines. Recombinant EA.hy926 cell lines in which IFI6 was either over-expressed (IFI6+/+) or knocked-down (IFI6-/-) were generated. The activation of caspase-3 and intrinsic apoptosis-related protein caspase-9 were down-regulated in IFI6+/+ but up-regulated in IFI6-/- cells at 24-48 hrs post-infection. After incubation with DENV for 48 hrs, the mitochondrial membrane potential (Δψ(m)) was more stable in IFI6+/+ cells but reduced in IFI6-/- cells, as assayed by fluorescence staining with JC-1. We observed that Bcl-2 expression was increased in IFI6+/+ and decreased in IFI6-/- cells. By contrast, Bax expression was decreased in IFI6+/+ and increased in IFI6-/- cells. It is presumed that the anti-apoptotic function of IFI6 is expressed by regulating the rheostatic balance between bcl-2/bax expression and inhibition of Δψ(m) depolarization during DENV infection of vascular endothelial cells(VECs). In addition, the pro-apoptotic protein X-linked Inhibitor of Apoptosis (XIAP)-Associated Factor 1(XAF1) expression had been reported to be up-regulated and led to the induction of apoptosis in DENV2-infected VECs,but the relationship between XAF1 and IFI6 dengue virus-induced apoptosis in VECs warrants further study. Dengue hemorrhagic fever (DHF)/Dengue shock syndrome (DSS) is a fatal infectious disease that demands an effective treatment. Interferon (IFN)-stimulated genes (ISGs) induced by dengue virus (DENV) exert antiviral effects. Among ISGs, IFN-[alpha] inducible gene 6 (IFI6) was increased in DENV infected human umbilical vascular endothelial cells (HUVECs) by microarray analysis in our previous study. However, its function is incompletely understood. In this study, we confirmed that IFI6 was markedly induced in DENV infection of both primary HUVECs and EA.hy926 cell lines. Recombinant EA.hy926 cell lines in which IFI6 was either over-expressed (IFI6+/+) or knocked-down (IFI6-/-) were generated. The activation of caspase-3 and intrinsic apoptosis-related protein caspase-9 were down-regulated in IFI6+/+ but up-regulated in IFI6-/- cells at 24-48 hrs post-infection. After incubation with DENV for 48 hrs, the mitochondrial membrane potential ([DELTA][psi](m)) was more stable in IFI6+/+ cells but reduced in IFI6-/- cells, as assayed by fluorescence staining with JC-1. We observed that Bcl-2 expression was increased in IFI6+/+ and decreased in IFI6-/- cells. By contrast, Bax expression was decreased in IFI6+/+ and increased in IFI6-/- cells. It is presumed that the anti-apoptotic function of IFI6 is expressed by regulating the rheostatic balance between bcl-2/bax expression and inhibition of [DELTA][psi](m) depolarization during DENV infection of vascular endothelial cells(VECs). In addition, the pro-apoptotic protein X-linked Inhibitor of Apoptosis (XIAP)-Associated Factor 1(XAF1) expression had been reported to be up-regulated and led to the induction of apoptosis in DENV2-infected VECs,but the relationship between XAF1 and IFI6 dengue virus-induced apoptosis in VECs warrants further study. |
Audience | Academic |
Author | Qi, Yiming Li, Ying Zhang, Yingke Zhang, Xuzhi Wang, Zilian Gui, Lian Zhang, Lin Huang, Junqi |
AuthorAffiliation | University of Rochester, UNITED STATES 1 Guangdong Provincial Key Laboratory of Organ Donation and Transplant Immunology, Guangzhou, PR China 2 First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China 4 Key Laboratory of Tropical Diseases Control, Ministry of Education, Guangzhou, PR China 3 Institute of Immunology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, PR China |
AuthorAffiliation_xml | – name: 3 Institute of Immunology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, PR China – name: 1 Guangdong Provincial Key Laboratory of Organ Donation and Transplant Immunology, Guangzhou, PR China – name: 4 Key Laboratory of Tropical Diseases Control, Ministry of Education, Guangzhou, PR China – name: 2 First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China – name: University of Rochester, UNITED STATES |
Author_xml | – sequence: 1 givenname: Yiming surname: Qi fullname: Qi, Yiming – sequence: 2 givenname: Ying surname: Li fullname: Li, Ying – sequence: 3 givenname: Yingke surname: Zhang fullname: Zhang, Yingke – sequence: 4 givenname: Lin surname: Zhang fullname: Zhang, Lin – sequence: 5 givenname: Zilian surname: Wang fullname: Wang, Zilian – sequence: 6 givenname: Xuzhi surname: Zhang fullname: Zhang, Xuzhi – sequence: 7 givenname: Lian surname: Gui fullname: Gui, Lian – sequence: 8 givenname: Junqi surname: Huang fullname: Huang, Junqi |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/26244642$$D View this record in MEDLINE/PubMed |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Conceived and designed the experiments: JH. Performed the experiments: YQ YL YZ. Analyzed the data: YQ YZ LG. Contributed reagents/materials/analysis tools: JH ZW. Wrote the paper: YQ YL LZ XZ. Competing Interests: The authors have declared that no competing interests exist. |
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Snippet | Dengue hemorrhagic fever (DHF)/Dengue shock syndrome (DSS) is a fatal infectious disease that demands an effective treatment. Interferon (IFN)-stimulated genes... |
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SubjectTerms | Apoptosis Apoptosis - genetics BAX protein Bcl-2 protein bcl-2-Associated X Protein - genetics bcl-2-Associated X Protein - metabolism Biological response modifiers Biotechnology Care and treatment Caspase Caspase-3 Caspase-9 Cell Line Cell lines Dengue - virology Dengue fever Dengue hemorrhagic fever Dengue Virus Depolarization Diagnosis DNA microarrays Down-Regulation Endothelial cells Endothelial Cells - metabolism Endothelial Cells - virology Endothelium Endothelium, Vascular - metabolism Endothelium, Vascular - virology Fever Fluorescence Genomics Health aspects Human Umbilical Vein Endothelial Cells - drug effects Human Umbilical Vein Endothelial Cells - metabolism Human Umbilical Vein Endothelial Cells - virology Humans Incubation Infections Infectious diseases Interferon Kinases Medical treatment Membrane potential Mitochondria Mitochondria - genetics Mitochondria - metabolism Mitochondrial Proteins - genetics Mitochondrial Proteins - metabolism Protein X Proteins Proto-Oncogene Proteins c-bcl-2 - genetics Proto-Oncogene Proteins c-bcl-2 - metabolism Risk factors Signal Transduction - genetics Tropical diseases Up-Regulation Vector-borne diseases Viral diseases Viruses X-Linked Inhibitor of Apoptosis Protein - genetics X-Linked Inhibitor of Apoptosis Protein - metabolism XIAP protein α-Interferon |
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Title | IFI6 Inhibits Apoptosis via Mitochondrial-Dependent Pathway in Dengue Virus 2 Infected Vascular Endothelial Cells |
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