Figure 3 - Recovery and activated phenotype of CD4+CD25+Foxp3+ thymocytes in Tgfbr1f/fLck-Cre+ mice.


From the following article

A critical function for TGF-beta signaling in the development of natural CD4+CD25+Foxp3+ regulatory T cells

Yongzhong Liu, Pin Zhang, Jun Li, Ashok B Kulkarni, Sylvain Perruche & WanJun Chen

Nature Immunology 9, 632 - 640 (2008) Published online: 27 April 2008 Corrected online: 4 May 2008

doi:10.1038/ni.1607

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(a) Expression of CD25 and Foxp3 by gated CD4+CD8- thymocytes from Tgfbr1f/fLck-Cre+ mice (n = 11) and control mice (n = 13) at the age of 3–4 weeks. (b) Percent CD4+Foxp3+ thymocytes (mean plusminus s.d.) in the CD4+ population of the mice in a. *, P = 0.0011. 'Tgfbr1+/+ or Tgfbr1f/+Lck-Cre+' includes Tgfbr1+/+Lck-Cre+ and Tgfbr1f/+Lck-Cre+ control mice. Data are representative of three experiments. (c) CD25 expression by CD4+Foxp3+ thymocytes from 2- to 4-week-old Tgfbr1f/fLck-Cre+ and control mice, presented as mean fluorescence intensity (MFI) plusminus s.d. of five mice (Tgfbr1f/fLck-Cre+) or seven mice (control). *, P = 0.012. This experiment was repeated four times with similar results. (d) Expression of activation markers on gated CD4+Foxp3+ thymocytes. Data are from one representative mouse from each group of at least three mice; this experiment was repeated more than three times.

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