Effects of continuous and released compressive force on osteoclastogenesis in vitro
Objective: Compressive force has been found to be catabolic to alveolar bone during orthodontic tooth movement. This study quantified the fusion of mononuclear RAW 264.7 cells (a murine osteoclastic-like cell line) into multinucleated osteoclasts under a hydrostatic pressure-generated mechanical com...
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Elsevier,
2024-03-01T00:00:00Z.
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LEADER | 00000 am a22000003u 4500 | ||
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001 | doaj_cb18a1cbb77a40e6bdf109edc5643d6c | ||
042 | |a dc | ||
100 | 1 | 0 | |a Boontida Changkhaokham |e author |
700 | 1 | 0 | |a Sumit Suamphan |e author |
700 | 1 | 0 | |a Suwanna Jitpukdeebodintra |e author |
700 | 1 | 0 | |a Chidchanok Leethanakul |e author |
245 | 0 | 0 | |a Effects of continuous and released compressive force on osteoclastogenesis in vitro |
260 | |b Elsevier, |c 2024-03-01T00:00:00Z. | ||
500 | |a 2212-4268 | ||
500 | |a 10.1016/j.jobcr.2024.01.015 | ||
520 | |a Objective: Compressive force has been found to be catabolic to alveolar bone during orthodontic tooth movement. This study quantified the fusion of mononuclear RAW 264.7 cells (a murine osteoclastic-like cell line) into multinucleated osteoclasts under a hydrostatic pressure-generated mechanical compression-the new model of various magnitudes and durations. Methods: RAW 264.7 cells were subjected to 0.3, 0.6 or 0.9 g/cm2 of compressive force by an acrylic cylinder custom-made by laser cutting or no compressive force for 4 days during osteoclastogenic induction. TRAP-positive multinucleated cells were quantified. For the release from force experiment, osteoclastogenesis was induced by 0.6 g/cm2 mechanical stimuli for 0, 1, 2, 3 or 4 days. Cell viability, TRAP-positive multinucleated cells, DCSTAMP and Cathepsin K (CTSK) gene expression were evaluated 4 days after release from force. Results: Compressive force at 0.6 and 0.9 g/cm2 significantly increase the number of TRAP-positive multinucleated cells (P < 0.05). Release from continuous mechanical compression after 4 days significantly elevated the number of TRAP-positive multinucleated cells and DCSTAMP and CTSK mRNA expression, with no adverse effects on cell viability (P < 0.05). Conclusions: Continuous stimulation with compressive force induced osteoclastogenesis in RAW 264.7 cells by enhancing DCSTAMP and CTSK expression, which provides new understanding of bone remodeling during orthodontic treatment. | ||
546 | |a EN | ||
690 | |a Cathepsin K | ||
690 | |a Compressive force | ||
690 | |a DCSTAMP | ||
690 | |a Osteoclasts | ||
690 | |a TRAP | ||
690 | |a Dentistry | ||
690 | |a RK1-715 | ||
655 | 7 | |a article |2 local | |
786 | 0 | |n Journal of Oral Biology and Craniofacial Research, Vol 14, Iss 2, Pp 164-168 (2024) | |
787 | 0 | |n http://www.sciencedirect.com/science/article/pii/S221242682400023X | |
787 | 0 | |n https://doaj.org/toc/2212-4268 | |
856 | 4 | 1 | |u https://doaj.org/article/cb18a1cbb77a40e6bdf109edc5643d6c |z Connect to this object online. |