TABLE 2.
Mean channel fluorescence of CD26 before and after stimulationa
Cells | Mean channel fluorescence value (SD)
|
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---|---|---|---|---|---|---|---|
Day 0 (control) | Day 6
|
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Control | IL-1α | TNF-α | IFN-γ | PMA | LPS | ||
HGF | 5.66 (0.42) | 9.29 (0.47) | 26.36 (5.35) | 15.77 (0.8) | 14.67 (0.92) | 17.70 (1.71) | 12.94 (1.91) |
PDL fibroblasts | 5.30 | 5.58 | 6.33 | NDb | 9.35 | ND | 4.07 |
Induction of CD26 on the cell surfaces of HGF and PDL fibroblasts in response to various stimulants is shown. Confluent HGF (donor, YS-G) and PDL fibroblasts (donor, AK) were stimulated with IL-1α (10 ng/ml), TNF-α (40 ng/ml), IFN-γ (200 U/ml), PMA (100 ng/ml), or E. coli LPS (10 μg/ml) for 6 days in α-MEM supplemented with 10% FCS. After being harvested by trypsinization, cells were stained with anti-CD26 MAb and analyzed by fluorescence-activated cell sorting. The results are representative of four different experiments with four different donors (YS-G, NIK, AK-G, and KEK) for HGF and three different experiments with three different donors (AK, TT, and YS) for PDL fibroblasts. Triplicate (HGF) and single (PDL fibroblasts) assays were carried out.
ND, not done.