4.8 Article

Nano-micrometer surface roughness gradients reveal topographical influences on differentiating responses of vascular cells on biodegradable magnesium

Journal

BIOACTIVE MATERIALS
Volume 6, Issue 1, Pages 262-272

Publisher

KEAI PUBLISHING LTD
DOI: 10.1016/j.bioactmat.2020.08.004

Keywords

Surface roughness gradients; Topography cue; Vascular cells; Cell adhesion and proliferation; Cell selectivity

Funding

  1. National Key Research and Development Program of China [2016YFC1102401, 2016YFB0301001]
  2. National Natural Science Foundation of China [51701041]
  3. Committee of Shanghai Science and Technology [17DZ2200200]
  4. Shanghai Outstanding Academic Leaders Plan [17XD1402100]

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By developing surface gradients with varying nano-micro roughness on magnesium, a study on the response of endothelial cells and smooth muscle cells was conducted, revealing significant differences between the two cell types in highly rough regions. Surface topography played a crucial role in overcoming the biochemical cues and was found to modulate cell response. Insights into the regulatory mechanism at subcellular and gene levels were also gained through this research.
Distinctively directing endothelial cells (ECs) and smooth muscle cells (SMCs), potentially by surface topography cue, is of central importance for enhancing bioefficacy of vascular implants. For the first time, surface gradients with a broad range of nano-micrometer roughness are developed on Mg, a promising next-generation biodegradable metal, to carry out a systematic study on the response of ECs and SMCs. Cell adhesion, spreading, and proliferation are quantified along gradients by high-throughput imaging, illustrating drastic divergence between ECs and SMCs, especially in highly rough regions. The profound role of surface topography overcoming the biochemical cue of released Mg2+ is unraveled at different roughness ranges for ECs and SMCs. Further insights into the underlying regulatory mechanism are gained at subcellular and gene levels. Our work enables high-efficient exploration of optimized surface morphology for modulating favored cell selectivity of promoting ECs and suppressing SMCs, providing a potential strategy to achieve rapid endothelialization for Mg.

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