Beta-Amyloid peptide and amyloid precursor proteins in olfactory mucosa of patients with Alzheimer's disease, Parkinson's disease, and Down syndrome

Ann Otol Rhinol Laryngol. 1995 Aug;104(8):655-61. doi: 10.1177/000348949510400812.

Abstract

Dystrophic neurites are present in olfactory epithelium (OE) of patients with Alzheimer's disease (AD), Parkinson's disease (PD), and Down syndrome (DS) and occasionally in normal individuals. Cultured olfactory neuroblasts from AD patients generate carboxy terminal amyloid precursor protein (APP) fragments that contain beta-amyloid (A beta), but it is not known if deposits of A beta and/or APP fragments occur in the OE of individuals with or without AD, PD, or DS. To determine if A beta accumulates in the OE in situ, we probed postmortem samples of olfactory mucosa from patients with AD, PD, and AD (PD/AD), and DS and AD (DS/AD), as well as from controls, using polyclonal and monoclonal antibodies to A beta and flanking sequences in APPs. Samples of OE also were examined by thioflavin-S and electron microscopy. Labeling of A beta was observed in 10 of 12 AD cases, 2 of 3 PD/AD cases, 3 of 4 DS/AD cases, 3 of 10 adult controls, and 4 of 6 fetal cases. The A beta staining was seen in the basal third of the OE, in axons projecting through the lamina propria, and in metaplastic respiratory epithelium within the OE. Antibodies to other APP domains stained the OE of patients and controls. Thioflavin-S staining was present in the basal third of the OE of 8 of 9 AD patients and several PD/AD and DS/AD patients, but only in rare cells of 3 controls. Electron microscopy did not reveal amyloid fibrils in the OE.(ABSTRACT TRUNCATED AT 250 WORDS)

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aged
  • Alzheimer Disease / metabolism
  • Alzheimer Disease / pathology*
  • Amyloid / analysis*
  • Amyloid beta-Peptides / analysis*
  • Case-Control Studies
  • Down Syndrome / metabolism
  • Down Syndrome / pathology*
  • Fetus / pathology
  • Humans
  • Immunohistochemistry
  • Infant
  • Infant, Newborn
  • Middle Aged
  • Nasal Mucosa / chemistry*
  • Parkinson Disease / metabolism
  • Parkinson Disease / pathology*
  • Prion Proteins
  • Prions
  • Protein Precursors / analysis*

Substances

  • Amyloid
  • Amyloid beta-Peptides
  • PRNP protein, human
  • Prion Proteins
  • Prions
  • Protein Precursors