Skip to main content
. 2023 Feb 8;220(4):e20221288. doi: 10.1084/jem.20221288

Figure 4.

Figure 4.

Ablating CTCF impairs TEFF cell accumulation and cytotoxic functions. (A) Immunoblotting for CTCF in sorted WT or Ctcf−/− GFP+ naive CD8+ T cells (before adoptive transfer, left) and early TEFF cells (4 dpi from infected recipients), with β-actin as loading control. Data are representative from two independent experiments. (B and C) Cell division of CTV-labeled WT or Ctcf−/− naive CD45.2+GFP+CD8+ T cells at 36 h (top) or 60 h (bottom) after transfer into CD45.1+ recipient mice followed by LCMV-Arm infection, with representative dot plots (B) and cumulative data on cell frequency in each cell division (C) shown. (D and E) Relative expression of CD25 (D) and CD69 (E) in WT or Ctcf−/− CD8+ T cells in individual cell divisions at 36 or 60 h after infection. gMFI, geometric mean fluorescence intensity. (F) Numbers of WT or Ctcf−/− effector CD8+ T cells on 4 and 8 dpi. (G–I) Detection of CD25 expression (G), IFN-γ production (H), and granzyme B expression (I) in WT or Ctcf−/− CD8+ T cells on 4 dpi. Data in B, H, and I are from two independent experiments. Data in C–F are means ± SD. *, P < 0.05; **, P < 0.01; ***, P < 0.001; NS, not statistically significant by two-tailed Student’s t test. Source data are available for this figure: SourceData F4.