4.6 Article

Nanosheet-pore topographical titanium substrates: a biophysical regulator of the fate of mesenchymal stem cells

Journal

JOURNAL OF MATERIALS CHEMISTRY B
Volume 4, Issue 10, Pages 1797-1810

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c5tb02391b

Keywords

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Funding

  1. National Natural Science Foundation of China [51173216, 31170923]
  2. Natural Science Foundation of Chongqing Municipal Government [CSTC2013kjrc-ljrcpy0004, CSTC2013jjB50004]
  3. National Key Technology R&D Program of the Ministry of Science and Technology [2012BAI18B04]
  4. Fundamental Research Funds for the Central Universities [CQDXWL-2013-Z002]

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Recent reports have demonstrated that nano- or micro-scale topography could enhance the cellular functions of stem cells. In this study, a sub-micrometer topography composed of nanosheet-pore structures was fabricated on the pure titanium surface by a simple vapor alkaline-treatment method to understand more profoundly sub-micrometer topography mediated stem cell behaviors. The topography was characterized by scanning electron microscopy, atomic force microscopy, X-ray photoelectron spectroscopy, X-ray diffraction and contact angle measurements, respectively. It specifically mediated cellular functions of rat bone marrow-derived mesenchymal stem cells (MSCs) on cellular and molecular levels under either normal medium or osteoinductive medium conditions. The experimental results indicated that the topography dramatically promoted the adhesion of MSCs grown on the surface, but the shape, morphology and spreading of cells were not significantly affected. In addition, the study demonstrated that the formation of focal adhesion complexes (FAs) were highly dependent on the topography, which in turn affects the subsequent biological functions of MSCs, especially accelerating osteogenic differentiation of MSCs under different conditions. Overall, the sub-micrometer topographical titanium substrate was an excellent biophysical regulator of the fate of mesenchymal stem cells, specifically inducing their differentiation into osteoblasts.

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