Department of Prosthetics, Stomatology Hospital, College of Medical Sciences, Zhejiang University, Hangzhou, China.
Mol Cell Biochem. 2010 Oct;343(1-2):183-90. doi: 10.1007/s11010-010-0512-8. Epub 2010 Jun 12.
This study was designed to investigate the effect of various strengths and action times of flow stress on mRNA expression of H+-ATPase in osteoclasts. Osteoclasts were obtained through a classical mechanical-anatomical technique. They were identified by their morphology, tartrate-resistant acid phosphatase (TRAP) staining, and by a test of their ability to form resorption lacunae. Osteoclasts were mechanically loaded by flow stress using a cell-loading system. The stress-loading experiments were divided into various strength groups and action time groups. The morphological changes of osteoclasts after application of loading stress were analyzed using an image analysis system and Image-Pro Plus software. Expression of H+-ATPase mRNA in osteoclasts was detected by real-time fluorescent quantitative polymerase chain reaction. The existence of significant differences between experimental groups was analyzed using SPSS 12.0 software. The cytoplasm of osteoclasts with positive TRAP staining appeared with a characteristic claret-red color. Cells were able to form resorption pits in the surface of dentine slices. Morphological changes of osteoclasts with applied stress assumed an early increasing tendency before reaching a peak value and following a decreasing tendency. A significant difference of H+-ATPase mRNA expression of osteoclasts was seen between any two groups (P < 0.05). H+-ATPase mRNA expression in osteoclasts had a tendency to first increase with increasing stress and was observed to then decrease in one action time group. In this present study, a close relationship between the stress and mRNA expression of H+-ATPase in osteoclasts was observed.
本研究旨在探讨不同强度和作用时间的流动应力对破骨细胞 H+-ATPase mRNA 表达的影响。通过经典的机械解剖技术获得破骨细胞,通过其形态、抗酒石酸酸性磷酸酶(TRAP)染色和形成吸收陷窝的能力进行鉴定。使用细胞加载系统通过流动应力对破骨细胞进行机械加载。应力加载实验分为不同的强度组和作用时间组。使用图像分析系统和 Image-Pro Plus 软件分析加载应力后破骨细胞的形态变化。通过实时荧光定量聚合酶链反应检测破骨细胞中 H+-ATPase mRNA 的表达。使用 SPSS 12.0 软件分析实验组之间存在显著差异。经 TRAP 染色呈阳性的破骨细胞细胞质呈现出典型的紫红色。细胞能够在牙本质切片表面形成吸收凹坑。施加应力后破骨细胞的形态变化呈现出先增加后减少的早期增加趋势。破骨细胞 H+-ATPase mRNA 表达在任何两个组之间均存在显著差异(P < 0.05)。在一个作用时间组中,破骨细胞中 H+-ATPase mRNA 的表达呈先增加后减少的趋势,随着应力的增加而增加。在本研究中,观察到破骨细胞中 H+-ATPase 与应力之间存在密切关系。