Figure 1
Figure 1. Inactivation of Smad4 in TECs causes thymic hypoplasia. (A) Representative photomicrographs of thymi from neonate (i), 5-week- (ii), and 20-week-old (iii) Smad4co/co (*) and Smad4co/co;Foxn1Cre (**) mouse littermates. Boxed area is shown in higher magnification to point out cysts in aged Smad4co/co;Foxn1Cre mice. Scale bars represent 1 mm. (B) Smad4 exon 9 deletion was verified in adult MHCIIint and MHCIIhi sorted TEC populations. Rectangles in the dot plots indicate sorting gates. Deletion was quantified by genomic PCR, yielding a 3-kb WT fragment and a 0.5-kb recombined fragment.

Inactivation of Smad4 in TECs causes thymic hypoplasia. (A) Representative photomicrographs of thymi from neonate (i), 5-week- (ii), and 20-week-old (iii) Smad4co/co (*) and Smad4co/co;Foxn1Cre (**) mouse littermates. Boxed area is shown in higher magnification to point out cysts in aged Smad4co/co;Foxn1Cre mice. Scale bars represent 1 mm. (B) Smad4 exon 9 deletion was verified in adult MHCIIint and MHCIIhi sorted TEC populations. Rectangles in the dot plots indicate sorting gates. Deletion was quantified by genomic PCR, yielding a 3-kb WT fragment and a 0.5-kb recombined fragment.

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