4.7 Article

Magnetically actuated cell-laden microscale hydrogels for probing strain-induced cell responses in three dimensions

期刊

NPG ASIA MATERIALS
卷 8, 期 -, 页码 -

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/am.2015.148

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资金

  1. National Natural Science Foundation of China [11372243, 11522219, 11532009]
  2. Major International Joint Research Program of China [11120101002]
  3. International Science and Technology Cooperation Program of China [2013DFG02930]
  4. Research Fund for the Doctoral Program of Higher Education of China [20130201120071]
  5. China Postdoctoral Science Foundation [2013M540742]
  6. China Young 1000-Talent Program
  7. Program for New Century Excellent Talents in University [NCET-12-0437]

向作者/读者索取更多资源

Living cells respond to their mechanical microenvironments during development, healing, tissue remodeling and homeostasis attainment. However, this mechanosensitivity has not yet been established definitively for cells in three-dimensional (3D) culture environments, in part because of challenges associated with providing uniform and consistent 3D environments that can deliver a large range of physiological and pathophysiological strains to cells. Here, we report microscale magnetically actuated, cell-laden hydrogels (mu MACs) for investigating the strain-induced cell response in 3D cultures. mu MACs provide high-throughput arrays of defined 3D cellular microenvironments that undergo reversible, relatively homogeneous deformation following non-contact actuation under external magnetic fields. We present a technique that not only enables the application of these high strains (60%) to cells but also enables simplified microscopy of these specimens under tension. We apply the technique to reveal cellular strain-threshold and saturation behaviors that are substantially different from their 2D analogs, including spreading, proliferation, and differentiation. mu MACs offer insights for mechanotransduction and may also provide a view of how cells respond to the extracellular matrix in a 3D manner.

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