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. 2023 May 15;24(7):e56131. doi: 10.15252/embr.202256131

Figure 2. L. monocytogenes capture instructs B cells to become antigen cross‐presenting cells.

Figure 2

  • A–D
    CD80 (A, B) and CD86 (C, D) expression in B cells measured by flow cytometry on day 0 (non‐instructed; naïve) and day 2 after L. monocytogenes capture (BacB). (A and C) show representative experiments, (B and D) show the mean of at least three independent experiments.
  • E, F
    H‐2Kb expression in B cells measured by flow cytometry on day 0 (naïve, pale gray) and day 1 after L. monocytogenes capture (BacB; dark gray). (E) Shows a representative experiment, (F) shows the mean of four independent experiments.
  • G, H
    Expression of OVAp‐I in the context of H‐2Kb was detected by flow cytometry with anti‐OVAp‐I/H‐2Kb antibody, comparing BacB capturing Listeria‐WT (pale gray) and Listeria‐OVA (dark gray). (G) Shows a representative experiment, (H) shows the mean of two independent experiments.
  • I
    Confocal images of Listeria‐WT (left panels) or Listeria‐OVA (right panels) BacB cells incubated with naïve OTI CD8+ T cells previously stained with CellTraceViolet (CV, red). Actin and CD3 fluorescence are shown on a “fire” scale and in cyan and white respectively in the merged images. Scale bars = 10 μm. *Indicate CD8+ T cells. Arrow points to the IS.
  • J
    Quantification of actin accumulation at the IS on CD8+ T cells conjugated with Listeria‐WT or Listeria‐OVA BacB cells, analyzed using Synapse measures software from confocal images. Each dot corresponds to one IS. Three independent experiments were performed.

Data information: Column bars in the figure represent the mean. Error bars indicate the SD. Significant differences, analyzed by t‐test are represented by asterisk; *P < 0.05, ***P < 0.0005, non‐significant differences are marked as (ns).

Source data are available online for this figure.