4.6 Article

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

Journal

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbrc.2020.03.146

Keywords

Mesenchymal stromal cells (MSCs); Atomic force microscopy (AFM); Osteogenic differentiation; Young's modulus; Substrate stiffness

Funding

  1. Ministry of Science and Technology [MOST 107-2911-I-010-504, MOST 107-2314-B-010-015-MY3, MOST 108-2911-I-010-502, MOST 108-2321B-010-006, MOST 108-2923-B-010-002-MY3]
  2. Development and Construction Plan of the School of Medicine, National Yang-Ming University [107F-M010504]
  3. Aiming for the Top University Plan from Ministry of Education

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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. (C) 2020 Elsevier Inc. All rights reserved.

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