4.6 Article

Responsive Inverse Opal Scaffolds with Biomimetic Enrichment Capability for Cell Culture

Journal

RESEARCH
Volume 2019, Issue -, Pages -

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.34133/2019/9783793

Keywords

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Funding

  1. National Key Research and Development Program of China [2017YFA0700404]
  2. National Natural Science Foundation of China [21473029, 51522302]
  3. NSAF Foundation of China [U1530260]
  4. National Science Foundation of Jiangsu Province [BK20180128]
  5. Scientific Research Foundation of Southeast University
  6. Scientific Research Foundation of the Graduate School of Southeast University
  7. Fundamental Research Funds for the Central Universities [2242018R20012]
  8. China Postdoctoral Science Foundation [2018M640445]

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Three-dimensional (3D) porous scaffolds have a demonstrated value for tissue engineering and regenerative medicine. Inspired by the predation processes of marine predators in nature, we present new photocontrolled shrinkable inverse opal graphene oxide (GO) hydrogel scaffolds for cell enrichment and 3D culture. The scaffolds with adjustable pore sizes and morphologies were created using a GO and N-isopropylacrylamide dispersed solution as a continuous phase of microfluidic emulsions for polymerizing and replicating. Because of the interconnected porous structures and the remotely controllable volume responsiveness of the scaffolds, the suspended cells could be enriched into the inner spaces of the scaffolds through predator-like swallowing and discharging processes. Hepatocyte cells concentrated in the scaffold pores could form denser 3D spheroids more quickly via the controlled compression force caused by the shrinking of the dynamic scaffolds. More importantly, with a program of scaffold enrichment with different cells, an unprecedented 3D multilayer coculture system of endothelial-cellencapsulated hepatocytes and fibroblasts could be generated for applications such as liver-on-a-chip and bioartificial liver. It was demonstrated that the resultant multicellular system offered significant improvements in hepatic functions, such as albumin secretion, urea synthesis, and cytochrome P450 expression. These features of our scaffolds make them highly promising for the biomimetic construction of various physiological and pathophysiological 3D tissue models, which could be used for understanding tissue level biology and in vitro drug testing applications.

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