The use of a laser for correlating light and electron microscopic images in thick tissue specimens

Methods Cell Biol. 2014:124:323-37. doi: 10.1016/B978-0-12-801075-4.00015-X.

Abstract

Correlating images between light and electron microscopy is difficult especially in tissue specimens with a substantial z-dimension. To facilitate correlated light and electron microscopy (CLEM) in thick tissue specimens, we describe a basic method of using a femto-pulsed near-infrared laser to burn precise three-dimensional fiducial markers that circumscribe cells or regions of interest for easy identification between imaging methods. This rapid and reliable approach permits traditional fixation and avoids the use of electron-dense labeling methods that can obscure ultrastructural details. The versatility of the technique permits CLEM in a variety of tissue specimens to allow interpretation of highly resolved ultrastructural data in the more macroscopic and potentially dynamic context of light microscopy.

Keywords: Confocal microscopy; Electron microscopy; In vivo; Multiphoton microscopy; Serial section reconstruction; Technique.

MeSH terms

  • Animals
  • Cerebral Cortex / ultrastructure
  • Imaging, Three-Dimensional*
  • Mice, Transgenic
  • Microscopy, Confocal / methods
  • Microscopy, Electron, Transmission / methods
  • Microtomy