Vascularization of hollow channel-modified porous silk scaffolds with endothelial cells for tissue regeneration

Biomaterials. 2015 Jul:56:68-77. doi: 10.1016/j.biomaterials.2015.03.053. Epub 2015 Apr 15.

Abstract

Despite the promise for stem cell-based tissue engineering for regenerative therapy, slow and insufficient vascularization of large tissue constructs negatively impacts the survival and function of these transplanted cells. A combination of channeled porous silk scaffolds and prevascularization with endothelial cells was investigated to test the ability of this tissue engineering strategy to support rapid and extensive vascularization process. We report that hollow channels promote in vitro prevascularization by facilitating endothelial cell growth, VEGF secretion, and capillary-like tube formation. When implanted in vivo, the pre-established vascular networks in the hollow channel scaffolds anastomose with host vessels and exhibit accelerated vascular infiltration throughout the whole tissue construct, which provides timely and sufficient nutrients to ensure the survival of the transplanted stem cells. This tissue engineering strategy can promote the effective application of stem cell-based regeneration to improve future clinical applications.

Keywords: Cell survival; Cell tracking; Regenerative medicine; Silk fibroin; Vascularization.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biocompatible Materials / chemistry*
  • Bombyx
  • Bone Marrow Cells / cytology
  • Cell Survival
  • Cell Transplantation
  • Fibroins / chemistry*
  • Human Umbilical Vein Endothelial Cells
  • Humans
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Neovascularization, Physiologic*
  • Porosity
  • Regeneration*
  • Tissue Engineering / methods*
  • Tissue Scaffolds / chemistry*
  • Vascular Endothelial Growth Factor A / metabolism
  • X-Ray Microtomography

Substances

  • Biocompatible Materials
  • Vascular Endothelial Growth Factor A
  • Fibroins