The integration of 3-D cell printing and mesoscopic fluorescence molecular tomography of vascular constructs within thick hydrogel scaffolds

Biomaterials. 2012 Jul;33(21):5325-32. doi: 10.1016/j.biomaterials.2012.04.004. Epub 2012 Apr 22.

Abstract

Developing methods that provide adequate vascular perfusion is an important step toward engineering large functional tissues. Meanwhile, an imaging modality to assess the three-dimensional (3-D) structures and functions of the vascular channels is lacking for thick matrices (>2 ≈ 3 mm). Herein, we report on an original approach to construct and image 3-D dynamically perfused vascular structures in thick hydrogel scaffolds. In this work, we integrated a robotic 3-D cell printing technology with a mesoscopic fluorescence molecular tomography imaging system, and demonstrated the capability of the platform to construct perfused collagen scaffolds with endothelial lining and to image both the fluid flow and fluorescent-labeled living endothelial cells at high-frame rates, with high sensitivity and accuracy. These results establish the potential of integrating both 3-D cell printing and fluorescence mesoscopic imaging for functional and molecular studies in complex tissue-engineered tissues.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Blood Vessel Prosthesis*
  • Cell Culture Techniques / methods*
  • Collagen / pharmacology
  • Fluorescence
  • Human Umbilical Vein Endothelial Cells / cytology
  • Human Umbilical Vein Endothelial Cells / drug effects
  • Human Umbilical Vein Endothelial Cells / metabolism
  • Humans
  • Hydrogel, Polyethylene Glycol Dimethacrylate / pharmacology*
  • Imaging, Three-Dimensional
  • Microscopy, Phase-Contrast
  • Perfusion
  • Phantoms, Imaging
  • Rats
  • Reproducibility of Results
  • Tissue Engineering / methods*
  • Tissue Scaffolds / chemistry*
  • Tomography / methods*

Substances

  • Hydrogel, Polyethylene Glycol Dimethacrylate
  • Collagen