School of Materials Science and Engineering, Nanyang Technological University, Singapore 639798, Singapore.
Biochem Biophys Res Commun. 2010 Feb 26;393(1):150-5. doi: 10.1016/j.bbrc.2010.01.107. Epub 2010 Feb 1.
Human mesenchymal stem cells (hMSCs) have gained widespread attention in the field of tissue engineering but not much is known about the changes of mechanical properties during the process of cell lineage commitment and the mechanisms of these behaviors. It is believed that exploring the inter-relations between stem cells mechanical properties and lineage commitment will shed light on the mechanobiology aspect of differentiation. hMSCs were cultured in adipogenic and osteogenic mediums and the elastic moduli were monitored using micropipette aspiration. It was found that hMSCs undergoing osteogenesis have an instantaneous Young's modulus of 890 +/- 219 Pa and an equilibrium Young's modulus of 224 +/- 40 Pa, each is about 2-fold higher than the control group. Interestingly, cells cultured in adipogenic medium exhibited a slight increase in the cellular modulus followed by a decrease relative to that of the control group. Gene expression study was employed to gain insights into this phenomenon. Concomitant up regulation of actin binding filamin A (FLNa) and gamma-Tubulin with the cellular elastic modulus indicated their important role in mechanical regulation during hMSCs differentiation. Statistical results showed that cell shape and cell area changed with cellular mechanical properties, which means that cell morphology has a close relation with cell elastic modulus in the initial stage of differentiation. Collectively, these results provide a quantitative description of hMSCs mechanical behavior during the process of differentiation as well as the possible accompanying mechanism at the biomolecular level.
人骨髓间充质干细胞(hMSCs)在组织工程领域受到广泛关注,但对于细胞谱系分化过程中力学性能的变化及其机制知之甚少。人们相信,探索干细胞力学特性与谱系分化之间的关系,将有助于阐明分化的力学生物学方面。我们将 hMSCs 培养在成脂和成骨培养基中,并使用微吸管抽吸法监测弹性模量。结果发现,成骨分化的 hMSCs 的瞬时杨氏模量为 890 ± 219 Pa,平衡杨氏模量为 224 ± 40 Pa,分别约为对照组的 2 倍。有趣的是,在成脂培养基中培养的细胞的细胞模量先略有增加,然后相对于对照组降低。我们通过基因表达研究来深入了解这种现象。细胞中肌动蛋白结合细丝蛋白 A(FLNa)和γ-微管蛋白的同时上调,表明它们在 hMSCs 分化过程中的力学调节中发挥重要作用。统计结果表明,细胞形状和细胞面积随细胞力学性能而变化,这意味着在分化的初始阶段,细胞形态与细胞弹性模量密切相关。综上所述,这些结果为 hMSCs 在分化过程中的力学行为提供了定量描述,以及在生物分子水平上可能伴随的机制。