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首页> 外文期刊>Connective tissue research >Effects of cyclic mechanical stretching on the mRNA expression of tendon/ligament-related and osteoblast-specific genes in human mesenchymal stem cells.
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Effects of cyclic mechanical stretching on the mRNA expression of tendon/ligament-related and osteoblast-specific genes in human mesenchymal stem cells.

机译:周期性机械拉伸对人间充质干细胞中肌腱/韧带相关和成骨细胞特异性基因mRNA表达的影响。

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The purpose of this study was to explore the influences of cyclic mechanical stretching on the mRNA expressions of tendon/ligament-related and osteoblast-specific marker genes in human MSCs seeded onto a collagen type I-coated surface. The stretch-induced mRNA expressions of mesenchymal stem cell protein (MSCP), matrix metalloproteinase-3 (MMP-3), and marker genes related to tendon/ligament cells (type I collagen, type III collagen, and tenascin-C) and those typical of osteoblasts (core binding factor alpha 1 (Cbfa1), alkaline phosphatase (ALP), and osteocalcin (OCN)) were analyzed by quantitative real-time PCR. The results revealed significant downregulation of MSCP and upregulation of MMP-3 genes in MSCs subjected to mechanical loading, regardless of the magnitude of the stretching (high or low). Moreover, the typical marker genes of the osteoblast lineage were upregulated by low-magnitude stretching, whereas tendon/ligament-related genes were upregulated by high-magnitude stretching for a long period. Cbfa1 and ALP were upregulated starting as early at 8 hr, followed by a downward trend and no significant change in expression at the other time points. The mRNA expressions of type I collagen, type III collagen, and tenascin-C significantly increased in MSCs subjected to 10% stretching for 48 hr, and this effect still existed after the stretched cells had rested for 48 hr. This study demonstrated the effect of cyclic mechanical stretching on differential transcription of marker genes related to different cell lineages. Low-magnitude stretching increased mRNA expressions of Cbfa1 and ALP and was possibly involved in the early osteoblastic differentiation of MSCs, whereas high-magnitude stretching upregulated the mRNA expressions of tendon/ligament-related genes.
机译:这项研究的目的是探讨循环机械拉伸对接种在I型胶原涂层表面的人MSC中肌腱/韧带相关和成骨细胞特异性标记基因mRNA表达的影响。拉伸诱导的间充质干细胞蛋白(MSCP),基质金属蛋白酶3(MMP-3)和与肌腱/韧带细胞相关的标志物基因(I型胶原,III型胶原和腱生蛋白C)的mRNA表达通过定量实时PCR分析典型的成骨细胞(核心结合因子α1(Cbfa1),碱性磷酸酶(ALP)和骨钙蛋白(OCN))。结果显示,受到机械负荷的MSC中,MSCP的显着下调和MMP-3基因的上调,而与拉伸的幅度(高或低)无关。此外,成骨细胞谱系的典型标记基因通过低强度拉伸被上调,而与肌腱/韧带相关的基因长期被高强度拉伸上调。 Cbfa1和ALP最早在8小时开始上调,随后呈下降趋势,在其他时间点表达无明显变化。在经过10%拉伸48小时的MSC中,I型胶原蛋白,III型胶原蛋白和腱糖蛋白C的mRNA表达显着增加,并且在拉伸的细胞静置48小时后这种效应仍然存在。这项研究证明了循环机械拉伸对与不同细胞谱系有关的标记基因差异转录的影响。低强度拉伸增加了Cbfa1和ALP的mRNA表达,可能参与了MSC的成骨分化,而高强度拉伸则上调了肌腱/韧带相关基因的mRNA表达。

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