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Resolution: standard / high Figure 9.
Detection of CD26 by Fluorescence-activated cell sorting (FACS) analysis. Expression of CD26 was detected by FACS analysis. (a) Expression level of CD26 on unstimulated fibroblasts. Background staining with secondary
antibody only (black histograms) was compared with specific CD26-staining (open histograms).
Control staining with isotype antibodies resulted in a similar histogram as with secondary
antibody alone. Confluent fibroblast monolayers were left untreated (Co) or were treated
with IL-1β (100 U/ml), tumour necrosis factor alpha (TNF-α) (10 ng/ml), IFN-γ (200
ng/ml) or with combinations of these cytokines. (b) Regulation of CD26 expression as the percentage of the relative mean fluorescence
intensity (MFI) for untreated fibroblasts (± standard error of the mean). The mean
MFI of four experiments is shown (except for treatment with IFN-γ alone, for which
n = 3). Statistical analysis was performed with the Mann–Whitney U test, *P < 0.05.
Proost et al. Arthritis Research & Therapy 2006 8:R107 doi:10.1186/ar1997 |