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Resolution: standard / high Figure 2.
p38 MAPK activity regulates cell death induced by anti-CD95. (a) Total cell death rate for OA chondrocytes quantified by trypan blue exclusion assay
after treatment of cells as indicated below. *P < 0.05 versus control. The graph shows the average of three independent experiments.
(b) Apoptosis rate of OA chondrocytes quantified by flow cytometry. Chondrocytes were
fluorescently labeled by TUNEL assay after treatment of cells as indicated below.
The data shown are representative of three OA cartilage samples. Anti-CD95: treatment
with a mAb anti-Fas CH 11 (100 ng/ml) in serum-free medium for 17 hours. SB: treatment
with SB203580 (10 μmol/l) for 17 hours. SB+Anti-CD95: treatment with SB203580 for
2 hours followed by anti-Fas treatment for 17 hours. Control: cells were treated with
DMSO only. (c) Chondrocytes were labeled with Hoechst after treatment of cells as indicated above.
Nuclear condensation (indicated by an arrow) was detected in the cells treated with
Anti-CD95. DMSO, dimethyl sulfoxide; mAb, monoclonal antibody; MAPK, mitogen-activated
protein kinase; OA, osteoarthritis; PI, propidium iodide; TUNEL, terminal dUTP nick-end
labeling.
Wei et al. Arthritis Research & Therapy 2006 8:R37 doi:10.1186/ar1891 |