压缩应力联合机械振动对RAW 264.7细胞破骨细胞生成的影响。

Boontida Changkhaokham, Sumit Suamphan, P. Pavasant, Suwanna Jitpukdeebodintra, C. Leethanakul
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引用次数: 0

摘要

目的探讨压缩力和/或机械振动对小鼠破骨样细胞系RAW 264.7细胞中NFATc1、DCSTAMP和CTSK (cathepsin K)基因表达和TRAP阳性多核细胞数量的影响。材料与方法对sraw 264.7细胞进行机械振动、压缩力或压缩力与振动的联合作用。测定细胞活力和trap阳性多核细胞数量。实时定量逆转录聚合酶链反应分析NFATc1、DCSTAMP、CTSK基因表达。结果压缩力联合机械振动可显著增加trap阳性多核细胞的数量,但对细胞活力无显著影响。此外,与单独压缩力或振动相比,压缩力联合机械振动显著增加了NFATc1、DCSTAMP和CTSK mRNA的表达。结论压缩力联合机械振动诱导RAW 264.7细胞破骨生成,上调NFATc1、DCSTAMP、CTSK基因表达。这些结果提供了更多的洞察机制,通过振动力加速正畸牙齿的运动。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of compressive stress combined with mechanical vibration on osteoclastogenesis in RAW 264.7 cells.
OBJECTIVES To investigate the effects of compressive force and/or mechanical vibration on NFATc1, DCSTAMP, and CTSK (cathepsin K) gene expression and the number of tartrate-resistant acid phosphatase (TRAP)-positive multinucleated cells in RAW 264.7 cells, a murine osteoclastic-like cell line. MATERIALS AND METHODS RAW 264.7 cells were subjected to mechanical vibration, compressive force, or compressive force combined with vibration. Cell viability and the numbers of TRAP-positive multinucleated cells were evaluated. NFATc1, DCSTAMP, and CTSK gene expressions were analyzed using real-time quantitative reverse transcription polymerase chain reaction. RESULTS Compressive force combined with mechanical vibration significantly increased the numbers of TRAP-positive multinucleated cells but did not significantly affect cell viability. In addition, compressive force combined with mechanical vibration significantly increased NFATc1, DCSTAMP, and CTSK mRNA expression compared with compressive force or vibration alone. CONCLUSIONS Compressive force combined with mechanical vibration induces osteoclastogenesis and upregulates NFATc1, DCSTAMP, and CTSK gene expression in RAW 264.7 cells. These results provide more insight into the mechanisms by which vibratory force accelerates orthodontic tooth movement.
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