Dalla-Bona Diego Araujo, Tanaka Eiji, Inubushi Toshihiro, Oka Hiroko, Ohta Atsumi, Okada Haruhisa, Miyauchi Mutsumi, Takata Takashi, Tanne Kazuo
Department of Orthodontics and Craniofacial Developmental Biology, Hiroshima University Graduate School of Biomedical Sciences, 1-2-3 Kasumi, Minami-Ku, Hiroshima 734-8553, Japan.
Arch Oral Biol. 2008 Apr;53(4):318-23. doi: 10.1016/j.archoralbio.2007.11.006. Epub 2007 Dec 27.
It has been shown that ultrasound stimulation accelerates repair of orthodontically induced root resorption. However, the mechanism of such adaptive change is still unclear. The purpose of this study was to evaluate pulsed ultrasound on the differentiation-potential and cementoblast-mediated osteoclastogenesis using a cementoblastic cell line.
Cultured cementoblasts (murine cementoblastic cell line, OCCM-30) were subjected to ultrasound exposure (frequency = 1 MHz; pulsed 1:4; spatial average temporal average intensities=30 or 150 mW/cm(2)) or sham exposure for 15 min per day. Expression levels of alkaline phosphatase (ALP), type I collagen (COL-I), osteoprotegerin (OPG) and receptor activator of nuclear factor small ka, CyrillicB ligand (RANKL) mRNAs were analysed by a real-time PCR analysis. Furthermore, ALP activity, collagen synthesis, and protein levels of OPG and RANKL were examined after 6-day ultrasound exposure.
Real-time PCR analysis indicated that, irrespective of the intensity, single ultrasound exposure increased the expression of transcripts for COL-I and ALP after 24h; the expression of OPG and RANKL also increased after 1 and 4h, respectively. Cultured cementoblasts receiving ultrasound stimulation for 6 days showed a significant (p<0.05 or 0.01) increase in cell number and collagen synthesis. ALP activity and OPG synthesis were also significantly (p<0.05) upregulated by ultrasound stimulation with 150 mW/cm(2).
These results demonstrated that ultrasound stimulation especially with 150 mW/cm(2) might be a better candidate as a medical remedy to protect against root resorption and/or accelerate its repair.
已有研究表明,超声刺激可加速正畸性牙根吸收的修复。然而,这种适应性变化的机制仍不清楚。本研究的目的是使用成牙骨质细胞系评估脉冲超声对分化潜能和成牙骨质细胞介导的破骨细胞生成的影响。
将培养的成牙骨质细胞(小鼠成牙骨质细胞系,OCCM-30)每天进行超声暴露(频率 = 1 MHz;脉冲 1:4;空间平均时间平均强度 = 30 或 150 mW/cm²)或假暴露 15 分钟。通过实时 PCR 分析碱性磷酸酶(ALP)、I 型胶原(COL-I)、骨保护素(OPG)和核因子κB 受体激活剂配体(RANKL)mRNA 的表达水平。此外,在超声暴露 6 天后检测 ALP 活性、胶原合成以及 OPG 和 RANKL 的蛋白水平。
实时 PCR 分析表明,无论强度如何,单次超声暴露在 24 小时后可增加 COL-I 和 ALP 转录本的表达;OPG 和 RANKL 的表达分别在 1 小时和 4 小时后也增加。接受超声刺激 6 天的培养成牙骨质细胞显示细胞数量和胶原合成显著(p<0.05 或 0.01)增加。150 mW/cm² 的超声刺激也显著(p<0.05)上调了 ALP 活性和 OPG 合成。
这些结果表明,超声刺激尤其是 150 mW/cm² 的超声刺激可能是预防牙根吸收和/或加速其修复的更好的医学治疗方法。