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Resolution: standard / high Figure 5.
Vpx and the proteasome inhibitor MG132, but not Arsenate, display similar effects
on the infection of DCs. A) DCs were either infected with Vpx-deficient SIVMAC or HIV-1 LVs (A and B, respectively, at MOI of 0.5 and 5) and treated singularly or
in combination with 1 μM arsenic acid (As2O3) and Vpx-VLPs (at MOI equivalents of 0,5 and 2,5). The efficiency of infection was
evaluated 72 hrs after by flow cytometry analysis. C) DCs were infected with Vpx containing
or deficient SIVMAC LVs (MOI 5) in presence or absence of MG132 (1 μg/ml). The drug was added 30 min prior
to infection then left for a total of 7 hrs prior to cell washing and media replacement.
DCs were then lysed at 24 hrs post-infection for FL PCR analysis as described in the
legend of Fig. 5A. Results are presented as a fold increase in FL DNA for each condition
with respect to the amount produced upon infection with Vpx-deficient SIVMAC LVs. D) DCs were similarly infected with a constant amount of HIV-1 LVs in presence
or absence of MG132 and 2 different amounts of Vpx-VLPs. Media was replaced 7 hrs
post-drug addition and cells analyzed 2 days afterwards by flow cytometry. One representative
experiment out of 3 is shown here for each panel.
Goujon et al. Retrovirology 2007 4:2 doi:10.1186/1742-4690-4-2 |