Development of senile plaques. Relationships of neuronal abnormalities and amyloid deposits

Am J Pathol. 1990 Dec;137(6):1383-92.

Abstract

The evolution of senile plaques and the relationships among neuritic elements, extracellular deposits of the beta-amyloid protein (beta/A4), and vascular beta/A4 are poorly understood. Immunocytochemical methods were used to examine fixed-frozen prefrontal cortices of 14 rhesus monkeys (Macaca mulatta) (14 to 37 years of age) for the presence of abnormal fibers/neurites, alpha 1-antichymotrypsin (alpha-ACT), and beta/A4. Age-associated alterations included abnormal fibers/neurites, presence of beta/A4, and association of alpha-ACT with beta/A4 in plaques and blood vessels. Vascular amyloid was present only in the oldest monkeys. The topographic distribution of abnormal fibers/neurites was mapped with acetylcholinesterase (AChE) histochemistry, and deposits of amyloid were visualized with immunocytochemistry for beta/A4. beta/A4 often was associated with neurites, but many neurites lacked demonstrable beta/A4. Thus in aged monkeys, abnormal neurites may provide one type of focus for the accumulation of the amyloid precursor, which is subsequently abnormally processed to form beta/A4. Our data in rhesus monkeys suggest that fiber and neuritic abnormalities increase with age and that they may precede the majority of beta/A4 deposits; the initial stages of neurite formation and parenchymal amyloid deposits may be independent of the appearance of vascular amyloid; and these processes may be synergistic with advanced age.

Publication types

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

MeSH terms

  • Acetylcholinesterase / metabolism
  • Aged
  • Aged, 80 and over
  • Aging / physiology*
  • Amyloid / metabolism*
  • Animals
  • Axons / metabolism
  • Axons / ultrastructure
  • Brain / metabolism
  • Brain / pathology
  • Histocytochemistry
  • Humans
  • Immunohistochemistry / methods
  • Macaca mulatta
  • Middle Aged
  • Neurofibrils / pathology
  • Neurons / pathology*
  • Staining and Labeling
  • alpha 1-Antichymotrypsin / metabolism

Substances

  • Amyloid
  • alpha 1-Antichymotrypsin
  • Acetylcholinesterase