Figure 4
Figure 4. Expression of MafB in adult thymus cells and nude 3PPs. (A) Quantitative PCR analysis of MafB transcript levels in indicated cell fractions isolated from adult C57BL/6 mice. MafB mRNA levels were normalized to GAPDH mRNA levels and are indicated as the ratio to the amount expressed in CD45+ leukocytes. Means and standard errors of the results obtained from 4 independent measurements are shown. (B) Quantitative PCR analysis of MafB and PD-L1 transcript levels in microdissected 3PPs from E11.5 nu/+ mice or E11.5 nu/nu mice. mRNA levels were normalized to GAPDH mRNA levels and are indicated as the ratio to the amount expressed in nu/+ 3PPs. Means and standard errors of the results obtained from 3 independent measurements are shown. (C) In situ expression analysis of MafB in developing thymus by monitoring GFP expression (green) derived from the MafB− allele, in which the coding sequence of MafB was replaced with GFP, of MafB+/− heterozygous mice.31 Paraformaldehyde-fixed E15.5 thymus sections were stained with anti-pancytokeratin antibody (red). Scale bars indicate 100 μm. Representative results of 10 different sections are shown.

Expression of MafB in adult thymus cells and nude 3PPs. (A) Quantitative PCR analysis of MafB transcript levels in indicated cell fractions isolated from adult C57BL/6 mice. MafB mRNA levels were normalized to GAPDH mRNA levels and are indicated as the ratio to the amount expressed in CD45+ leukocytes. Means and standard errors of the results obtained from 4 independent measurements are shown. (B) Quantitative PCR analysis of MafB and PD-L1 transcript levels in microdissected 3PPs from E11.5 nu/+ mice or E11.5 nu/nu mice. mRNA levels were normalized to GAPDH mRNA levels and are indicated as the ratio to the amount expressed in nu/+ 3PPs. Means and standard errors of the results obtained from 3 independent measurements are shown. (C) In situ expression analysis of MafB in developing thymus by monitoring GFP expression (green) derived from the MafB allele, in which the coding sequence of MafB was replaced with GFP, of MafB+/− heterozygous mice.31  Paraformaldehyde-fixed E15.5 thymus sections were stained with anti-pancytokeratin antibody (red). Scale bars indicate 100 μm. Representative results of 10 different sections are shown.

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