Confocal imaging protocols for live/dead staining in three-dimensional carriers

Methods Mol Biol. 2011:740:127-40. doi: 10.1007/978-1-61779-108-6_14.

Abstract

In tissue engineering, a variety of methods are commonly used to evaluate survival of cells inside tissues or three-dimensional (3D) carriers. Among these methods confocal laser scanning microscopy opened accessibility of 3D tissue using live cell imaging into the tissue or 3D scaffolds. However, although this technique is ideally applied to 3D tissue or scaffolds with thickness up to several millimetres, this application is surprisingly rare and scans are often done on slices with thickness <20 μm. Here, we present novel protocols for the staining of 3D tissue (e.g. intervertebral disc tissue) and scaffolds, such as fibrin gels or alginate beads.

MeSH terms

  • Animals
  • Cattle
  • Cell Proliferation / drug effects
  • Cell Separation
  • Cell Survival / drug effects
  • Chondrocytes / cytology
  • Chondrocytes / drug effects
  • Fibrin / pharmacology
  • Imaging, Three-Dimensional / methods*
  • Injections
  • Intervertebral Disc / cytology
  • Intervertebral Disc / drug effects
  • Mesenchymal Stem Cell Transplantation
  • Mesenchymal Stem Cells / cytology
  • Mesenchymal Stem Cells / drug effects
  • Mesenchymal Stem Cells / metabolism
  • Microscopy, Confocal / methods*
  • Organic Chemicals / metabolism
  • Solutions
  • Staining and Labeling*

Substances

  • Organic Chemicals
  • PKH 26
  • Solutions
  • Fibrin