Characterization of metabolic changes associated with the functional development of 3D engineered tissues by non-invasive, dynamic measurement of individual cell redox ratios

Biomaterials. 2012 Jul;33(21):5341-8. doi: 10.1016/j.biomaterials.2012.04.024. Epub 2012 May 4.

Abstract

Non-invasive approaches to assess tissue function could improve significantly current methods to diagnose diseases and optimize engineered tissues. In this study, we describe a two-photon excited fluorescence microscopy approach that relies entirely on endogenous fluorophores to dynamically quantify functional metabolic readouts from individual cells within three-dimensional engineered tissues undergoing adipogenic differentiation over six months. Specifically, we employ an automated approach to analyze 3D image volumes and extract a redox ratio of metabolic cofactors. We identify a decrease in redox ratio over the first two months of culture that is associated with stem cell differentiation and lipogenesis. In addition, we demonstrate that the presence of endothelial cells facilitate greater cell numbers deeper within the engineered tissues. Since traditional assessments of engineered tissue structure and function are destructive and logistically intensive, this non-destructive, label-free approach offers a potentially powerful high-content characterization tool for optimizing tissue engineering protocols and assessing engineered tissue implants.

Publication types

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

MeSH terms

  • Adipose Tissue / cytology
  • Azo Compounds / metabolism
  • Cell Differentiation
  • Cell Proliferation
  • Cells, Cultured
  • Coculture Techniques
  • Endothelial Cells / cytology
  • Endothelial Cells / metabolism*
  • Flavin-Adenine Dinucleotide / metabolism
  • Humans
  • Image Processing, Computer-Assisted
  • Lipid Metabolism
  • Mesenchymal Stem Cells / cytology
  • Mesenchymal Stem Cells / metabolism*
  • Microscopy, Fluorescence, Multiphoton
  • Microvessels / cytology
  • Models, Biological
  • NAD / metabolism
  • Oxidation-Reduction
  • Staining and Labeling
  • Time Factors
  • Tissue Engineering / methods*

Substances

  • Azo Compounds
  • NAD
  • Flavin-Adenine Dinucleotide
  • oil red O