|
Resolution: standard / high Figure 5.
CHOP plays an important role in autophagy in RASF and in cell death in OASF. OASF and RASF were treated with thapsigargin (5 μM) or tunicamycin (5 μg/ml) for
60 h. Autophagy formation was measured as described in methods *P < 0.05, significantly different from thapsigargin-treated OASF, #P < 0.05, significantly different from tunicamycin-treated OASF (a). Non-specific or CHOP siRNA was transfected into OASF and RASF. After 16 h, cells
were treated with thapsigargin (5 μM) or tunicamycin (5 μg/ml) for 4 h. Immunoblotting
was performed with anti-CHOP or actin antibody (b). Autophagy formation (c) and cell death (d) were measured. *P < 0.05, significantly different from non-specific siRNA-transfected OASF in the presence
of thapsigargin. #P < 0.05, significantly different from non-specific siRNA-transfected OASF in the presence
of tunicamycin, $P < 0.05, significantly different from non-specific siRNA-transfected RASF in the presence
of thapsigargin. &P < 0.05, significantly different from non-specific siRNA-transfected RASF in the presence
of tunicamycin.
Shin et al. Arthritis Research & Therapy 2010 12:R19 doi:10.1186/ar2921 |