Immunohistochemistry and microwave decalcification of human temporal bones

Hear Res. 2000 Oct;148(1-2):192-6. doi: 10.1016/s0378-5955(00)00153-2.

Abstract

Processing of human temporal bones is a long, expensive process and the resulting celloidin sections are difficult to use for immunohistochemistry. We tested the ability of immunohistochemical assays to work in human temporal bones that were decalcified using a microwave oven. Tissue was trimmed to an approximate cube (1.5-2 cm/side) containing only the cochlea and immersed in fresh EDTA with paraformaldehyde every 6 h. This sized block required 190-400 h to decalcify. The decalcified tissue was embedded in paraffin and sectioned. Sections were immunoassayed with anti-cytochrome c oxidase, anti-neurofilament or anti-peripherin. All three antibodies labeled the appropriate structures. This procedure may stimulate advancement in the understanding of human inner ear pathology.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Calcium / antagonists & inhibitors*
  • Calcium / metabolism
  • Cochlea / metabolism
  • Cochlea / radiation effects
  • Electron Transport Complex IV / metabolism
  • Humans
  • Immunohistochemistry
  • Intermediate Filament Proteins / metabolism
  • Membrane Glycoproteins*
  • Microwaves*
  • Nerve Tissue Proteins / metabolism
  • Neurofilament Proteins / metabolism
  • Peripherins
  • Temporal Bone / metabolism*
  • Temporal Bone / radiation effects*

Substances

  • Intermediate Filament Proteins
  • Membrane Glycoproteins
  • Nerve Tissue Proteins
  • Neurofilament Proteins
  • PRPH protein, human
  • Peripherins
  • Electron Transport Complex IV
  • Calcium