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. 2008 May 12;112(3):626–634. doi: 10.1182/blood-2007-10-115618

Figure 4.

Figure 4

The absence of TGFβ signaling in TECs results in an increase in mature, single-positive thymocytes. (A) Relative frequency of phenotypically mature (ie, CD3high) thymocytes in 8-week-old TGFβRIIlox/lox::Foxn1-Cre (□) and TGFβRIIlox/lox (■) mice. (B) Relative frequency of CD3high SP thymocytes in E12.5 thymic lobes of phenotypically mature thymocytes in TGFβRIIlox/lox::Hoxa3-Cre (□) and TGFβRIIlox/lox (■) embryos grafted under the kidney capsule of syngeneic nude recipients and analyzed 12 weeks later. (C) Relative frequency of CD24low and (D) absolute numbers of CD24low (Inline graphic) and CD24high (Inline graphic) thymocytes among single-positive, CD3high thymocytes in TGFβRIIlox/lox::Foxn1-Cre and TGFβRIIlox/lox mice. (E) Thymic export measured by intrathymic FITC injection of 5-week-old mice and quantification of FITC+ cells 24 hours later: absolute number of FITC+ T cells detected in spleen and lymph nodes (Inline graphic CD4+ T cells, Inline graphicCD8+ T cells). One of 3 experiments with similar results shown. P values were obtained using a t test. Error bars represent SD.