At each time points as indicated, the fluorescent dyes (2.0 μM) were added into the culture media and cells were incubated for 15 min before micro-images were taken Apoptosis inhibitor under a fluorescent microscope (panel A, magnification × 200). Quantitative data for the percentage of dead cells (red-labeled cells) in the total cells (red plus green cells) were summarized in panel B as mean ± SEM from 5 microscopic fields). The asterisk indicates a significant difference (P < 0.01, Student t -test) as compared to the value at the 0 hour time point. The calcimimetic R-568-induced cell death is an apoptotic event in prostate cancer cells It has been shown that CaSR activation is involved in osteoblast

cell apoptosis [4] and R-568 treatment induces apoptotic

cell death in rat parathyroid cell [3]. Therefore, we asked if R-568-induced cell death was an apoptotic selleck chemicals response in LNCaP and PC-3 cells. We utilized the most commonly used apoptotic markers, www.selleckchem.com/products/BIRB-796-(Doramapimod).html caspase-3 processing and PARP cleavage, in our next experiments. As shown in Fig 3 (panel A and panel B), R-568 treatment resulted in a remarkable processing of caspase-3 and a clear pattern of PARP cleavage in both LNCaP and PC-3 cells, indicating that R-568-induced cell death is an apoptotic response. Figure 3 R-568-induced cell death is an apoptotic response in prostate cancer cells. A&B LNCaP and PC-3 cells were treated with R-568 (50 μM) for different time period as indicated. Equal amounts of cellular proteins were subjected to Western blot assay to assess caspase-3 processing and PARP cleavage. Primary antibodies used are indicated on the left side. Actin blot served as the protein loading control. Data represent two different experiments. C LNCaP and PC-3 cells were seeded in 8-well chambered glass slides overnight. Following treatment with R-568 or S-568 at a dose of 50 μM for 24 h, cells were incubated with JC-1 (0.3 μg/ml) for 15 min Rebamipide at 37C. Pictures were

taken under a fluorescent microscope. Magnification × 200. To further characterize R-568-induced apoptosis, we examined the change of mitochondrial membrane potential using the JC-1 dye, which accumulates in the mitochondria of viable cells as aggregates, which are fluorescent red in color. Conversely, in apoptotic cells, the mitochondrial potential collapses and the JC-1 dye could no longer accumulate in the mitochondria and remains in the cytoplasm in a monomeric form which fluoresces green. As shown in Fig 3C, treatment with R-568 but not S-568 induced a dramatic change of JC-1 color/distribution from red/puncture pattern to green/defused pattern, suggesting that R-568 treatment induced a severe damage to mitochondria, which is consistent with the data shown in Fig 3A and Fig 3B. Taken together, these data strongly suggest that the calcimimetic agent R-568 induced apoptotic cell death via a mitochondria-related mechanism.