Scheven B A, Man J, Millard J L, Cooper P R, Lea S C, Walmsley A D, Smith A J
University of Birmingham School of Dentistry, St Chad's Queensway, Birmingham B46NN, UK.
Arch Oral Biol. 2009 Feb;54(2):185-91. doi: 10.1016/j.archoralbio.2008.09.008. Epub 2008 Nov 5.
Vascular endothelial growth factor (VEGF) has been implicated in the regulation of dental pulp and dentine repair. Therapeutic ultrasound was shown to be effective for fracture repair. We investigated whether low frequency ultrasound influences the production of VEGF by odontoblast-like cells. Moreover, we examined the direct effects of VEGF on odontoblast-like cell proliferation.
MDPC-23, an established odontoblast-like cell line, was exposed to increasing intensities of 30kHz ultrasound using an ultrasonic tip probe.
After 24h cell culture, WST-1 analysis of cell viability and number showed a dose-dependent decrease in the number of viable cells with increasing ultrasound power. However, the relative concentration of VEGF as analysed by ELISA and normalised to cell number was significantly increased in the culture supernatants indicating an ultrasound-induced stimulation of odontoblastic VEGF secretion. Analysis of VEGF gene expression by sqRT-PCR revealed the expression of the main VEGF isoforms in the MDPC-23 cells, i.e. VEGF(120) and VEGF(164) as well as to a minor extent VEGF(188). Low power ultrasound increased gene expression of all VEGF isoforms. Addition of recombinant VEGF to the cell cultures significantly stimulated cell proliferation. Gene expression of the VEGF receptors Flt1/VEGFR1 and KDR/VEGFR2 was detected in the MDPC-23, suggesting the possibility that VEGF may act on the odontoblast-like cells in an autocrine manner.
Our results indicate that ultrasound promoted VEGF expression and production by odontoblast-like cells and that VEGF may have autocrine effects on these cells. It is proposed that ultrasound may influence odontoblast activity and dentine repair by modulating production of endogenous growth factors in the dentine-pulp complex.
血管内皮生长因子(VEGF)与牙髓和牙本质修复的调节有关。治疗性超声已被证明对骨折修复有效。我们研究了低频超声是否会影响成牙本质细胞样细胞产生VEGF。此外,我们还检测了VEGF对成牙本质细胞样细胞增殖的直接影响。
使用超声探头将已建立的成牙本质细胞样细胞系MDPC-23暴露于强度不断增加的30kHz超声下。
细胞培养24小时后,通过WST-1分析细胞活力和数量发现,随着超声功率增加,活细胞数量呈剂量依赖性减少。然而,通过ELISA分析并以细胞数量标准化的VEGF相对浓度在培养上清液中显著增加,表明超声诱导了成牙本质细胞VEGF分泌。通过sqRT-PCR分析VEGF基因表达发现,MDPC-23细胞中主要的VEGF异构体即VEGF(120)和VEGF(164)以及少量的VEGF(188)均有表达。低功率超声增加了所有VEGF异构体的基因表达。向细胞培养物中添加重组VEGF可显著刺激细胞增殖。在MDPC-23中检测到VEGF受体Flt1/VEGFR1和KDR/VEGFR2的基因表达,提示VEGF可能以自分泌方式作用于成牙本质细胞样细胞。
我们的结果表明,超声促进了成牙本质细胞样细胞VEGF的表达和产生,且VEGF可能对这些细胞具有自分泌作用。有人提出,超声可能通过调节牙髓-牙本质复合体中内源性生长因子的产生来影响成牙本质细胞活性和牙本质修复。