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人羊水来源干细胞成骨分化过程中细胞力学的原子力显微镜研究

AFM studies of cellular mechanics during osteogenic differentiation of human amniotic fluid-derived stem cells.

作者信息

Chen Qian, Xiao Pan, Chen Jia-Nan, Cai Ji-Ye, Cai Xiao-Fang, Ding Hui, Pan Yun-Long

机构信息

Department of Chemistry, Jinan University, Guangzhou 510632, P. R. China.

出版信息

Anal Sci. 2010;26(10):1033-7. doi: 10.2116/analsci.26.1033.

Abstract

Amniotic fluid-derived stem cells (AFSCs) are becoming an important source of cells for regenerative medicine given with apparent advantages of accessibility, renewal capacity and multipotentiality. In this study, the mechanical properties of human amniotic fluid-derived stem cells (hAFSCs), such as the average Young's modulus, were determined by atomic force microscopy (3.97 ± 0.53 kPa for hAFSCs vs. 1.52 ± 0.63 kPa for fully differentiated osteoblasts). These differences in cell elasticity result primarily from differential actin cytoskeleton organization in these two cell types. Furthermore, ultrastructures, nanostructural details on the surface of cell, were visualized by atomic force microscopy (AFM). It was clearly shown that surface of osteoblasts were covered by mineralized particles, and the histogram of particles size showed that most of the particles on the surface of osteoblasts distributed from 200 to 400 nm in diameter, while the diameter of hAFSCs particles ranged from 100 to 200 nm. In contrast, there were some dips on the surface of hAFSCs, and particles were smaller than that of osteoblasts. Additionally, as osteogenic differentiation of hAFSCs progressed, more and more stress fibers were replaced by a thinner actin network which is characteristic of mature osteoblasts. These results can improve our understanding of the mechanical properties of hAFSCs during osteogenic differentiation. AFM can be used as a powerful tool for detecting ultrastructures and mechanical properties.

摘要

羊水来源的干细胞(AFSCs)因其在获取、更新能力和多能性方面具有明显优势,正成为再生医学中重要的细胞来源。在本研究中,通过原子力显微镜测定了人羊水来源的干细胞(hAFSCs)的力学性能,如平均杨氏模量(hAFSCs为3.97±0.53 kPa,而完全分化的成骨细胞为1.52±0.63 kPa)。这两种细胞弹性的差异主要源于这两种细胞类型中肌动蛋白细胞骨架组织的不同。此外,通过原子力显微镜(AFM)观察了细胞表面的超微结构和纳米结构细节。结果清楚地表明,成骨细胞表面覆盖有矿化颗粒,颗粒大小直方图显示,成骨细胞表面的大多数颗粒直径分布在200至400 nm之间,而hAFSCs颗粒的直径范围为100至200 nm。相比之下,hAFSCs表面有一些凹陷,且颗粒比成骨细胞的小。此外,随着hAFSCs向成骨细胞分化的进行,越来越多的应力纤维被成熟成骨细胞特有的较细肌动蛋白网络所取代。这些结果有助于我们更好地理解hAFSCs在成骨分化过程中的力学性能。AFM可作为检测超微结构和力学性能的有力工具。

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