Versatile fabrication of vascularizable scaffolds for large tissue engineering in bioreactor

Biomaterials. 2015 Mar:45:124-31. doi: 10.1016/j.biomaterials.2014.12.031. Epub 2015 Jan 29.

Abstract

Despite significant progresses were achieved in tissue engineering over the last 20 years, a number of unsolved problems still remain. One of the most relevant issues is the lack of a proper vascularization that is limiting the size of the engineered tissues to smaller than clinically relevant dimensions. Sacrificial molding holds great promise to engineered construct with perfusable vascular architectures, but there is still the need to develop more versatile approaches able to be independent of the nature and dimensions of the construct. In this work we developed a versatile sacrificial molding technique for fabricating bulk, cell-laden and porous scaffolds with embedded vascular fluidic networks. These branched fluidic architectures are created by highly resistant thermoplastic sacrificial templates, made of poly(vinyl alcohol), representing a remarkable progress in manufacturability and scalability. The obtained architecture, when perfused in bioreactor, has shown to prevent the formation of a necrotic core in thick cell-laden constructs and enabled the rapid fabrication of hierarchically branched endothelium. In conclusion we demonstrate a novel strategy towards the engineering of vascularized thick tissues through the integration of the PVA-based microfabrication sacrificial approach and perfusion bioreactors. This approach may be able to scale current engineered tissues to clinically relevant dimensions, opening the way to their widespread clinical applications.

Keywords: Bioreactor; Sacrificial molding; Scaffolds; Tissue engineering; Vascularization.

MeSH terms

  • Animals
  • Bioreactors*
  • Cell Survival
  • Endothelial Cells / drug effects
  • Endothelial Cells / metabolism
  • Fluorescent Antibody Technique
  • Gels
  • Mice
  • Microfluidics
  • Microtechnology
  • NIH 3T3 Cells
  • Neovascularization, Physiologic*
  • Optical Imaging
  • Porosity
  • Tissue Engineering / methods*
  • Tissue Scaffolds / chemistry*

Substances

  • Gels