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原子力显微镜测量间充质基质细胞成骨过程中杨氏模量的改变。

Alteration of Young's modulus in mesenchymal stromal cells during osteogenesis measured by atomic force microscopy.

机构信息

Institute of Clinical Medicine, and Stem Cell Research Center, National Yang-Ming University, Taipei, Taiwan; Department of Electronic Engineering, National Chin-Yi University of Technology, Taichung, Taiwan.

Institute of Biophotonics, National Yang-Ming University, Taipei, Taiwan.

出版信息

Biochem Biophys Res Commun. 2020 Jun 4;526(3):827-832. doi: 10.1016/j.bbrc.2020.03.146. Epub 2020 Apr 6.

Abstract

Mechanical properties of biological tissues are increasingly recognized as an important parameter for the indication of disease states as well as tissue homeostasis and regeneration. Multipotent mesenchymal stromal/stem cells (MSCs), which play important roles in bone formation and remodeling, are potential cell sources for regenerative medicine. However, the cellular mechanical properties of differentiating MSCs corresponding to the substrate stiffness has not been sufficiently studied. In this study, we used Atomic Force Microscopy (AFM) to measure changes of stiffness of human MSCs cultured in rigid Petri dish and on polyacrylamide (PA) substrates during osteogenic differentiation. The results showed that the Young's modulus of MSC cytoplasmic outer region increased over time during osteogenesis. There is a strong linear correlation between the osteogenic induction time and the Young's modulus of the cells cultured in rigid Petri dishes in the first 15 days after the induction; the Young's modulus approaches to a plateau after day 15. On the other hand, the Young's moduli of MSCs cultured on PA gels with stiffness of 7 kPa and 42 kPa also increase over time during osteogenic differentiation, but the inclination of such increase is much smaller than that of MSCs differentiating in rigid dishes. Herein, we established a protocol of AFM measurement to evaluate the maturation of stem cell osteogenic differentiation at the single cell level and could encourage further AFM applications in tissue engineering related to mechanobiology.

摘要

生物组织的力学性能正逐渐被认为是指示疾病状态以及组织动态平衡和再生的一个重要参数。多能间充质基质/干细胞(MSCs)在骨形成和重塑中发挥着重要作用,是再生医学的潜在细胞来源。然而,对于分化中的 MSCs 对应于基质刚度的细胞力学特性尚未进行充分研究。在这项研究中,我们使用原子力显微镜(AFM)来测量在成骨分化过程中培养在刚性培养皿和聚丙烯酰胺(PA)基质上的人 MSCs 的硬度变化。结果表明,在成骨过程中,MSC 细胞质外层的杨氏模量随时间增加。在诱导后的前 15 天,刚性培养皿中培养的细胞的成骨诱导时间与杨氏模量之间存在很强的线性相关性;15 天后杨氏模量趋于稳定。另一方面,在杨氏模量为 7 kPa 和 42 kPa 的 PA 凝胶上培养的 MSCs 也随着成骨分化时间的增加而增加,但这种增加的倾斜度远小于在刚性培养皿中分化的 MSCs。在此,我们建立了一种 AFM 测量方案,以评估单个细胞水平的干细胞成骨分化成熟度,并鼓励在与力学生物学相关的组织工程中进一步应用 AFM。

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