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Journal of Dental Research
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Figure 4


Figure 4. Effects on apoptotic signaling pathways by 15-d-PGJ2. Control cells were assigned a value of 1, and other values were expressed relative to these and were plotted against the time after 15-d-PGJ2 treatment. Data are expressed as mean ± SD (n = 3). *p < 0.05, **p < 0.01. (A) Caspase activation induced by 15-d-PGJ2. Cells were incubated with 20 µM 15-d-PGJ2 and troglitazone for the indicated periods of time. (B) Effects of caspase inhibitors on 15-d-PGJ2-induced apoptosis. Cells were treated with 20 µM 15-d-PGJ2 in the presence or absence of Z-VAD-FMK (2.5-20 µM), or Z-DEVD-FMK (2.5-20 µM) for 24 hrs. Then cells were processed for detection of fragmented mono- and oligonucleosomes by ELISA. (C) Cytochrome c release from mitochondria. Cells were incubated with 20 µM 15-d-PGJ2 for the indicated periods of time.

J DENT RES, Vol. 82, No. 10, 802-806 (2003)
DOI: 10.1177/154405910308201008





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