Fig. 5: TAGAP is important for T helper cell polarization in mice. | Nature Communications

Fig. 5: TAGAP is important for T helper cell polarization in mice.

From: TAGAP instructs Th17 differentiation by bridging Dectin activation to EPHB2 signaling in innate antifungal response

Fig. 5: TAGAP is important for T helper cell polarization in mice.

a Cells of lymph nodes and spleens from heterozygous control or TAGAP-deficient mice were analyzed by flow cytometry by gating on CD4+, and analyzed by IL-17A or IFN-γ-producing cells. Right panel indicates quantitative result, and the top right panel represents data from spleen, and the bottom right data represent data from lymph nodes (n = 8). b Heterozygous control or TAGAP-deficient mice were immunized subcutaneously with 200 μg MOG35–55 and 400 μg Mycobacteria tuberculosis H37RA in 200 μL of complete Freund’s adjuvant (Difco). Lymph nodes were collected 10 days later and single-cell suspensions were prepared. Cells were cultured with MOG35–55 (20 μg/mL) for another 3 days, followed by flow cytometry analysis of indicated cell populations. Right panel were quantitative results (n = 4). c Heterozygous control or TAGAP-deficient mice were immunized as in b, except for immunization with 200 μg MOG35–55 plus CFA and 400 μg heat-killed C. albicans (sc-5314). Right panel were quantitative results (n = 4). d Heterozygous control or TAGAP-deficient mice were immunized as in b, except for immunization with 200 μg MOG35–55 plus CFA only (n = 4). ns: P = 0.5226 and P = 0.288. e Naive CD4+ T cells were isolated from spleens of heterozygous control or TAGAP-deficient mice, and polarized in vitro for 3 days in the Th17 or Th1 cell polarization conditions. Cells were analyzed by flow cytometry by gating on CD4+, and analyzed by IL-17A or IFN-γ-producing cells. Right panel were quantitative results (n = 10). ns: P = 0.1848 and P = 0.9952. f Wild-type mice were injected intravenously with 2 × 105 live C. albicans (sc-5314) in 100 μL PBS. Ten days later, CD4+ T cells were isolated from spleen, and co-cultured with DCs isolated from heterozygous control or TAGAP-deficient mice for another 3 days together with indicated numbers of heat-killed C. albicans. Cells were analyzed by flow cytometry by gating on CD4+, and analyzed by IL-17A or IFN-γ-producing cells (n = 6). Right panel were qualified results. *P < 0.05; **P < 0.01; ***P < 0.001 based on two-sided unpaired t test a–f. All error bars represent SEM of technical replicates. Data are representative of two independent experiments.

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