Figure 4
Figure 4. Validation of changes in gene expression using quantitative RT-PCR and flow cytometry. (A-B) Fold change in the expression of selected genes measured by quantitative RT-PCR for (A) patients (P1-P3) relative to controls4 and (B) P1-yr +6 relative to P1-yr 0. P values were calculated based on 3 independent experiments using the Student t test and are indicated in the corresponding bar. (C) Histograms showing the surface expression of CD29 (ITGB1), CD49D (ITGA4), and CD62L (SELL) on control CD3+CD4+CD45RO+ T cells and P1-yr 0, P1-yr +4, and P1-yr +6 CD3−CD4+CD45RO+ T cells. Isotype controls (not shown) for each sample were set between 100 and 101.

Validation of changes in gene expression using quantitative RT-PCR and flow cytometry. (A-B) Fold change in the expression of selected genes measured by quantitative RT-PCR for (A) patients (P1-P3) relative to controls and (B) P1-yr +6 relative to P1-yr 0. P values were calculated based on 3 independent experiments using the Student t test and are indicated in the corresponding bar. (C) Histograms showing the surface expression of CD29 (ITGB1), CD49D (ITGA4), and CD62L (SELL) on control CD3+CD4+CD45RO+ T cells and P1-yr 0, P1-yr +4, and P1-yr +6 CD3CD4+CD45RO+ T cells. Isotype controls (not shown) for each sample were set between 100 and 101.

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