Immunohistochemical co-localization of S-100b and the glial fibrillary acidic protein in rat brain

Neuroscience. 1986 Mar;17(3):857-65. doi: 10.1016/0306-4522(86)90050-3.

Abstract

A rabbit antiserum against purified bovine brain S-100b protein was produced and characterized by immunoassay and immunoblot analysis of electrophoretically resolved soluble brain proteins. Fluorescent immunohistochemistry was conducted in order to determine the cellular localization of the S-100b immunoreactivity. Double immunohistofluorescent experiments on adult rat brain tissue sections with the rabbit antiserum to S-100b and a rat monoclonal antibody to the glial fibrillary acidic protein resulted in immunolabelling of the same cells. This finding determines a strict astroglial localization of the S-100b immunoreactivity. In addition, the immunolabelling of astrocyte perikarya and processes by the S-100b immunohistochemistry is consistent with a cytoplasmic location of S-100b. In contrast, the glial fibrillary acidic protein immunohistochemistry predominantly labeled the fine fibrillary processes of the cells. The present report suggests that S-100b immunohistochemistry is of use for the specific identification and morphological description of astrocytes in the rat brain.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Monoclonal
  • Astrocytes / analysis
  • Brain Chemistry*
  • Cattle
  • Enzyme-Linked Immunosorbent Assay
  • Fluorescent Antibody Technique
  • Glial Fibrillary Acidic Protein / analysis*
  • Immune Sera / analysis
  • Male
  • Neurons / analysis
  • Rabbits
  • Rats
  • S100 Proteins / analysis*
  • Staining and Labeling

Substances

  • Antibodies, Monoclonal
  • Glial Fibrillary Acidic Protein
  • Immune Sera
  • S100 Proteins