Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/71112
標題: HIV-1 Vpr Triggers Mitochondrial Destruction by Impairing Mfn2-Mediated ER-Mitochondria Interaction
作者: Huang, C.Y.
Chiang, S.F.
Lin, T.Y.
Chiou, S.H.
Chow, K.C.
關鍵字: viral protein r;virus type-1 vpr;tail-anchored proteins;cell-cycle;arrest;cytomegalovirus ul37 proteins;endoplasmic-reticulum;ubiquitin;ligase;nmr structure;subcellular-localization;nuclear-localization
Project: Plos One
期刊/報告no:: Plos One, Volume 7, Issue 3.
摘要: 
Human immunodeficiency virus 1 (HIV-1) viral protein R (Vpr) has been shown to induce host cell death by increasing the permeability of mitochondrial outer membrane (MOM). The mechanism underlying the damage to the mitochondria by Vpr, however, is not clearly illustrated. In this study, Vpr that is introduced, via transient transfection or lentivirus infection, into the human embryonic kidney cell line HEK293, human CD4(+) T lymphoblast cell line SupT1, or human primary CD4+ T cells serves as the model system to study the molecular mechanism of Vpr-mediated HIV-1 pathogenesis. The results show that Vpr injures MOM and causes a loss in membrane potential (MMP) by posttranscriptionally reducing the expression of mitofusin 2 (Mfn2) via VprBP-DDB1-CUL4A ubiquitin ligase complex, gradually weakening MOM, and increasing mitochondrial deformation. Vpr also markedly decreases cytoplasmic levels of dynamin-related protein 1 (DRP1) and increases bulging in mitochondria-associated membranes (MAM), the specific regions of endoplasmic reticulum (ER) which form physical contacts with the mitochondria. Overexpression of Mfn2 and DRP1 significantly decreased the loss of MMP and apoptotic cell death caused by Vpr. Furthermore, by employing time-lapse confocal fluorescence microscopy, we identify the transport of Vpr protein from the ER, via MAM to the mitochondria. Taken together, our results suggest that Vpr-mediated cellular damage may occur on an alternative protein transport pathway from the ER, via MAM to the mitochondria, which are modulated by Mfn2 and DRP1.
URI: http://hdl.handle.net/11455/71112
ISSN: 1932-6203
DOI: 10.1371/journal.pone.0033657
Appears in Collections:期刊論文

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