Chen Yi-Jane, Huang Chien-Hsun, Lee I-Chi, Lee Yu-Tsang, Chen Min-Huey, Young Tai-Horng
School of Dentistry, College of Medicine, National Taiwan University, Taipei, Taiwan.
Connect Tissue Res. 2008;49(1):7-14. doi: 10.1080/03008200701818561.
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.
本研究的目的是探讨周期性机械拉伸对接种于I型胶原包被表面的人骨髓间充质干细胞(MSCs)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。通过定量实时PCR分析了拉伸诱导的间充质干细胞蛋白(MSCP)、基质金属蛋白酶-3(MMP-3)以及与肌腱/韧带细胞相关的标记基因(I型胶原、III型胶原和腱生蛋白-C)和成骨细胞典型标记基因(核心结合因子α1(Cbfa1)、碱性磷酸酶(ALP)和骨钙素(OCN))的mRNA表达。结果显示,无论拉伸幅度大小(高或低),机械加载的MSCs中MSCP基因显著下调,MMP-3基因上调。此外,低幅度拉伸上调了成骨细胞谱系的典型标记基因,而高幅度长时间拉伸上调了肌腱/韧带相关基因。Cbfa1和ALP在8小时时就开始上调,随后呈下降趋势,在其他时间点表达无显著变化。在10%拉伸48小时的MSCs中,I型胶原、III型胶原和腱生蛋白-C的mRNA表达显著增加,并且在拉伸后的细胞静置48小时后这种效应仍然存在。本研究证明了周期性机械拉伸对不同细胞谱系相关标记基因差异转录的影响。低幅度拉伸增加了Cbfa1和ALP的mRNA表达,可能参与了MSCs的早期成骨分化,而高幅度拉伸上调了肌腱/韧带相关基因的mRNA表达。