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. Author manuscript; available in PMC: 2019 Jun 15.
Published in final edited form as: J Immunol. 2018 Apr 27;200(12):4012–4023. doi: 10.4049/jimmunol.1800112

Figure 1. Spontaneous lethal inflammation in mice with a Treg cell-specific deletion of talin.

Figure 1

(A and B) Morphology (A) or organs (B) (spleen, lymph nodes (aortic, brachial, mesenteric, inguinal), and thymi) of male Tln1fl/fl or Tln1fl/flFoxp3Cre mice. (C) H&E stains of lung, liver, heart, and skin tissue from Tln1fl/fl or Tln1fl/flFoxp3Cre mice. (D and E) Body weight from 4–10 weeks of age (D) and survival (E) of Tln1fl/fl or Tln1fl/flFoxp3Cre mice; n=10. (F–H) Percentages of splenic CD4+ or CD8+ T cells (F) expressing CD44, CD62L (G), or Ki-67 (H) from Tln1fl/fl or Tln1fl/flFoxp3Cre mice; displayed cells gated on CD4+ or CD8+ events; n=6. (I) IFNγ and TNFα expression by splenic CD4+ (left) and CD8+ (right) T cells from Tln1fl/fl or Tln1fl/flFoxp3Cre mice; displayed cells gated on CD4+CD44hi or CD8+CD44hi events; n=6. Data are mean ± SEM and representative of at least 2 independent experiments. *, P < 0.05; **, P <0.01, *** P <0.005, unpaired Student’s t-test.

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