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周期性拉伸对人牙周膜细胞成骨基因表达的影响。

Effect of the cyclic stretch on the expression of osteogenesis genes in human periodontal ligament cells.

机构信息

Department of Orthodontics, College of Stomatology, The Fourth Military Medical University, Xi'an, Shaanxi Province 710032, People's Republic of China.

出版信息

Gene. 2012 Jan 10;491(2):187-93. doi: 10.1016/j.gene.2011.09.031. Epub 2011 Oct 12.

Abstract

Periodontal ligament cells can potentially differentiate into osteoblast-like cells and influence the remodeling of periodontal tissues under mechanical strain conditions. In the present study, Gene chip technology was adopted to investigate the effect of the cyclic stretch on the expression of osteogenic-related genes in human periodontal ligament cells (HPDLCs). Cultured HPDLCs were subjected to 12% elongation cyclic stretch for 24 h using a Flexercell Strain Unit, and then GEArray Q series human osteogenesis gene expression profile chip with 96 spot array numbers was used to conduct parallel analyses on the change of the related gene expression in the osteogenic differentiation of HPDLCs stimulated by cyclic stretch. The results show that after the HPDLCs were stimulated by the cyclic stretch, the expression of 21 osteogenic-related genes was significantly upregulated, including 10 growth factor genes and their associated molecules, 10 extracellular matrix genes and their associated proteins, and 1 cell adhesion molecule. Two genes were significantly downregulated, including one growth factor gene and one cell adhesion molecule. Then the expressions of 10 candidate genes were validated using Real-time RT-PCR. These results indicate that cyclic stretch with 12% deformation can stimulate or inhibit some gene expression which was associated with the process of HPDLCs differentiation.

摘要

牙周膜细胞在机械应变条件下具有向成骨样细胞分化的潜能,并影响牙周组织的改建。本研究采用基因芯片技术观察周期性张应变对人牙周膜细胞(HPDLCs)成骨相关基因表达的影响。应用 Flexercell 应变装置对培养的 HPDLCs 施以 12%的伸长率周期性张应变 24 h,然后采用 GEArray Q 系列人类成骨基因表达谱芯片(96 点阵列数)平行分析周期性张应变刺激 HPDLCs 成骨分化过程中相关基因表达的变化。结果表明,HPDLCs 受周期性张应变刺激后,21 个成骨相关基因的表达明显上调,包括 10 个生长因子基因及其相关分子、10 个细胞外基质基因及其相关蛋白和 1 个细胞黏附分子;有 2 个基因表达明显下调,包括 1 个生长因子基因和 1 个细胞黏附分子。然后采用实时 RT-PCR 对 10 个候选基因的表达进行了验证。这些结果表明,12%变形的周期性张应变可以刺激或抑制与 HPDLCs 分化过程相关的某些基因的表达。

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