Fluorescence imaging of osteoclasts using confocal microscopy

Fraser Coxon

Research output: Contribution to journalArticle

Abstract

In order to understand osteoclast cell biology, it is necessary to culture these cells on a physiological -substrate that they can resorb in vitro, such as bone or dentine. However, this creates problems for analysis by fluorescence microscopy, due to the depth of the sample under investigation. By virtue of its optical sectioning capabilities, confocal microscopy is ideal for analysis of such samples, enabling precise intracellular localisation of proteins in resorbing osteoclasts to be determined. Moreover, by taking a series of images in the axial dimension, it is possible to create axial section views and to reconstruct 3D images of the osteoclasts, enabling the spatial organisation of the structures of interest to be more easily discerned.

Original languageEnglish
Pages (from-to)401-424
Number of pages24
JournalMethods in Molecular Biology
Volume816
Early online date14 Oct 2011
DOIs
Publication statusPublished - 2012

Fingerprint

Optical Imaging
Osteoclasts
Confocal Microscopy
Dentin
Fluorescence Microscopy
Cell Biology
Cell Culture Techniques
Bone and Bones
Proteins

Keywords

  • alendronate
  • animals
  • cells, cultured
  • dentin
  • equipment design
  • fluorescent dyes
  • humans
  • microscopy, confocal
  • osteoclasts
  • staining and labeling

Cite this

Fluorescence imaging of osteoclasts using confocal microscopy. / Coxon, Fraser.

In: Methods in Molecular Biology, Vol. 816, 2012, p. 401-424.

Research output: Contribution to journalArticle

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