Park et al. [160] analyzed the relevance of MAPK activation and reactive oxygen species (ROS)-induced apoptosis in MC3T3-E1 cells. http://www.selleckchem.com/products/z-vad-fmk.html We also

examined whether MAPKs play a role in osteocytes apoptosis, treating osteocytes with the ERK1/2 inhibitor, PD98059, and p38 MAPK inhibitor, SB239063, under compressive force loading [155]. PD98059 significantly blocked loading-induced osteocyte apoptosis, whereas SB239063 showed a trend, but not significant for reduced osteocyte apoptosis. These results indicate that compressive force loading induces osteocyte apoptosis through activation of MAPK, especially ERK1/2. However, we did not examine how ERK1/2 activation induces osteocyte apoptosis, which thus needs to be assessed in future investigations. Osteocytes produce various factors that mediate the onset of bone formation and resorption, and play roles in maintaining bone homeostasis and remodeling in response to

mechanical stimuli. Osteocytes are mechanosensors and mechanotransducers in bone. As explained in this article, we have shown previously that osteocytes respond to mechanical compressive force loaded on the bone with expression of the osteopontin gene during experimental tooth movement. Following the increased expression of OPN in osteocytes, a greater number of osteoclasts and numerous resorption pits were observed on the pressure side of the alveolar bone. Furthermore, an in vitro migration assay demonstrated the chemotactic activity of OPN on the precursor of osteoclasts. Thus, our study selleck inhibitor suggests that OPN is an important

migration factor for osteoclast precursor cells to bone surface, triggering bone resorption caused by mechanical compressive forces. In addition to OPN, experimental tooth movement stimulates the gene expression of CCN2/CTGF and induces apoptosis in osteocytes in mice. In that study, CTGF mRNA expression was detected at 2 h in osteocytes on the pressure side, followed by apoptosis at 6 h after tooth movement in mice and the number of empty lacunae significantly increased on day 1 after mechanical stimulation. Thereafter, the number of osteoclasts significantly increased on the pressure side of the alveolar bone on day 3. Finally, tooth movement increased rapidly on day 10. These findings suggest that CTGF expression, followed by apoptosis Thymidine kinase in osteocytes in response to mechanical compressive force might play a significant role for bone resorption on pressure side during tooth movement. CCN2 expression and production were promoted in isolated osteocytes in vitro under compressive force loading. The reinforced CCN2 induced osteocyte apoptosis through activation of ERK1/2 pathway. These results at least in part elucidated the mechanism of bone resorption under mechanical compressive force. Furthermore, we showed anti-apoptotic effect of CCN2 neutralizing antibody and ERK1/2 inhibitor, PD98059 in osteocytes under compressive force loading.