Abstract: The successful entry of human immunodeficiency virus type 1 (HIV-1) relies on
active functions of the viral envelope glycoproteins (Env) and human CD4 together with
proper chemokine co-receptors. To specifically search for novel HIV-1 entry inhibitors, we
established a cell-cell fusion assay that mimicked the entry step of the virus. The assay
utilized two cell populations; effector cells that expressed HIV-1 Env on the cell surface as
well as a trans-activator Tat protein, and target cells that expressed human CD4 and CXCR4
as viral receptor and co-receptor, respectively. To assess fusion, we exploited a copepod
Pontellina plumata green fluorescent protein (copGFP) to be expressed under the control of a
truncated HIV-1 LTR promoter in the target cells. By co-culturing the effector and the target
cells, multinucleated cells or syncytia were formed by 24 hours as a result of cell-cell fusion,
allowing Tat from the effector cells to activate the truncated LTR promoter in the target cells.
Therefore, the amounts of syncytial formations could be directly quantified by measuring
fluorescent intensity, which was demonstrated to be optimal on day 4 after co-cultivation.
The assay was validated by showing that cell-cell fusion mediated by HIV-1 Env was
inhibited by a known fusion inhibitor (enfuvirtide, T20) in a dose-dependent manner. The
50% inhibitory concentration (IC50) of T20 in our assay was 0.0242 μg/ml. These results
indicate that our system of HIV-1 Env-mediated cell-cell fusion assay is suitable for
identification and evaluation of potential HIV-1 entry inhibitors.
Abstract: The successful entry of human immunodeficiency virus type 1 (HIV-1) relies onactive functions of the viral envelope glycoproteins (Env) and human CD4 together withproper chemokine co-receptors. To specifically search for novel HIV-1 entry inhibitors, weestablished a cell-cell fusion assay that mimicked the entry step of the virus. The assayutilized two cell populations; effector cells that expressed HIV-1 Env on the cell surface aswell as a trans-activator Tat protein, and target cells that expressed human CD4 and CXCR4as viral receptor and co-receptor, respectively. To assess fusion, we exploited a copepodPontellina plumata green fluorescent protein (copGFP) to be expressed under the control of atruncated HIV-1 LTR promoter in the target cells. By co-culturing the effector and the targetcells, multinucleated cells or syncytia were formed by 24 hours as a result of cell-cell fusion,allowing Tat from the effector cells to activate the truncated LTR promoter in the target cells.Therefore, the amounts of syncytial formations could be directly quantified by measuringfluorescent intensity, which was demonstrated to be optimal on day 4 after co-cultivation.The assay was validated by showing that cell-cell fusion mediated by HIV-1 Env wasinhibited by a known fusion inhibitor (enfuvirtide, T20) in a dose-dependent manner. The50% inhibitory concentration (IC50) of T20 in our assay was 0.0242 μg/ml. These resultsindicate that our system of HIV-1 Env-mediated cell-cell fusion assay is suitable foridentification and evaluation of potential HIV-1 entry inhibitors.
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