Zhao Yanhong, Wang Chunling, Li Shu, Song Hui, Wei Fulan, Pan Keqing, Zhu Kun, Yang Pishan, Tu Qisheng, Chen Jake
School of Stomatology, Shandong University, Jinan, Shandong, China.
Eur J Oral Sci. 2008 Jun;116(3):199-206. doi: 10.1111/j.1600-0722.2008.00533.x.
Osterix (Osx) is an osteoblast-specific transcription factor required for the differentiation of pre-osteoblasts into functional osteoblasts. This study sought to examine the changes of Osx expression in periodontal ligament cells (PDLC) subjected to mechanical force, and to investigate whether Osx is involved in the mechanical stress-induced differentiation of PDLC. Human PDLC were exposed to centrifugal force for 1-12 h. Real-time polymerase chain reaction (PCR), western blot, and immunofluorescence assays were used to examine the mRNA and protein expression of Osx and its subcellular localization. Furthermore, PDLC were transfected with the expression vector pcDNA3.1 flag-Osx and subjected to mechanical force for 6 h. The changes in alkaline phosphatase (ALP) activity and in the expression of core-binding factor alpha1 (Cbfa1), ALP, osteopontin, bone sialoprotein, osteocalcin, and collagen I were measured. After the application of mechanical force, Osx was upregulated in a time-dependent manner at both mRNA and protein levels, and Osx protein was translocated from the cytosol into the cell nuclei. Overexpression of Osx did not affect the expression of Cbfa1, but it significantly enhanced the ALP activity and the mRNA expression of all the aforementioned osteogenic marker genes, all of which increased further under mechanical stress. These results suggest that Osx might play an important role in the mechanical stress-induced osteogenic differentiation of PDLC and therefore be involved in alveolar bone remodeling during orthodontic therapy.
osterix(Osx)是一种成骨细胞特异性转录因子,是前成骨细胞分化为功能性成骨细胞所必需的。本研究旨在检测牙周膜细胞(PDLC)在受到机械力作用时Osx表达的变化,并探讨Osx是否参与机械应力诱导的PDLC分化。将人PDLC暴露于离心力下1至12小时。采用实时聚合酶链反应(PCR)、蛋白质印迹法和免疫荧光测定法检测Osx的mRNA和蛋白质表达及其亚细胞定位。此外,用表达载体pcDNA3.1 flag-Osx转染PDLC,并使其受到机械力作用6小时。检测碱性磷酸酶(ALP)活性以及核心结合因子α1(Cbfa1)、ALP、骨桥蛋白、骨唾液蛋白、骨钙素和I型胶原表达的变化。施加机械力后,Osx在mRNA和蛋白质水平均呈时间依赖性上调,且Osx蛋白从细胞质转位至细胞核。Osx的过表达不影响Cbfa1的表达,但显著增强了上述所有成骨标记基因的ALP活性和mRNA表达,在机械应力作用下这些表达进一步增加。这些结果表明,Osx可能在机械应力诱导的PDLC成骨分化中起重要作用,因此参与正畸治疗期间的牙槽骨重塑。