Tocopherol-mediated modulation of age-related changes in microglial cells: turnover of extracellular oxidized protein material

Free Radic Biol Med. 2006 Jun 15;40(12):2126-35. doi: 10.1016/j.freeradbiomed.2006.02.011. Epub 2006 Mar 9.


Proteins accumulate during aging and form insoluble protein aggregates. Microglia are responsible for their removal from the brain. During aging, changes within the microglia might play a crucial role in the malfunctioning of these cells. Therefore, we isolated primary microglial cells from adult rats and compared their activation status and their ability to degrade proteins to that of microglial cells isolated from newborn animals. The ability of adult microglial cells to degrade proteins is substantially decreased. However, the preincubation of microglial cells with vitamin E improves significantly the degradation of such modified proteins. The degradation of proteins from apoptotic vesicles is decreased in microglia isolated from adult rats. This might be the result of a suppression of the CD36 receptor due to vitamin E treatment. We concluded that microglial cells isolated from adult organisms have different metabolic properties and seem to be a more valuable model to study age-related diseases.

Publication types

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

MeSH terms

  • Age Factors
  • Animals
  • Animals, Newborn
  • Apoptosis
  • CD36 Antigens / metabolism*
  • Lysosomes / metabolism
  • Microglia / drug effects*
  • Microglia / metabolism*
  • Myelin Basic Protein / metabolism
  • Proteasome Endopeptidase Complex / metabolism
  • Rats
  • Rats, Wistar
  • Tocopherols / pharmacology*


  • CD36 Antigens
  • Myelin Basic Protein
  • Proteasome Endopeptidase Complex
  • Tocopherols