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. 2021 May 10;95(11):e02124-20. doi: 10.1128/JVI.02124-20

FIG 2.

FIG 2

Correlation between HIV-1 vpu/env mRNA level and Env protein level. (A) Sorting strategy for Env-GFPBright, Env-GFPdim, and Env-GFP cells. Activated CD4+ T cells were infected with NL4-3ΔEnv-EGFP. Env-GFPBright, Env-GFPdim, and Env-GFP cells were sorted based on green fluorescent protein (GFP) intensity on day 3 postinfection. (B) Sorting strategy for IgG-FcBright, IgG-Fcdim, and GFP cells. Activated CD4+ T cells were infected with NL4-3-Env(Ba-L)-Δnef-EGFP. On day 3 postinfection, surface Env protein was labeled by PGT121 followed with anti-human IgG Fc antibodies. (C and D) Cell-associated vpu/env or gag mRNA was measured by qPCR. P values were calculated by one-way analysis of variance (ANOVA) with Tukey’s test. *, P < 0.05; **, P < 0.01; ***, P < 0.001; ****, P < 0.0001.