Cell cycle-related protein expression in vascular dementia and Alzheimer's disease

M Z Smith, Z Nagy, M M Esiri

Research output: Contribution to journalArticlepeer-review

81 Citations (Scopus)

Abstract

Recent findings from our and other laboratories indicate that cell cycle-related phenomena may play a key role in the formation of Alzheimer-type pathology and neuronal cell death in both Alzheimer's and cerebro-vascular diseases. In this study we examine the expression patterns of cyclins A, B1, D1 and E in neuronal nuclei in the hippocampus in autopsied healthy elderly individuals, Alzheimer's disease patients and subjects suffering from cerebrovascular disease with and without co-existing Alzheimer's disease. Nuclear cyclin B1 and cyclin E expression was detected in hippocampal neurones in each subject category. However, cyclin B1 expression was significantly elevated in the CA1 of patients suffering from cerebro-vascular disease alone, while cyclin E expression was significantly higher in the CA4 subfield in patients suffering from mixed Alzheimer's and cerebro-vascular diseases compared to subjects in other categories. We hypothesize that cell cycle re-entry may occur in healthy elderly people leading to age-related cell death and mild Alzheimer-type pathology in the hippocampus. However, in pathological conditions, the cell cycle arrest may lead either to the development of severe Alzheimer-related pathology or to excess apoptotic cell death as in vascular dementia.

Original languageEnglish
Pages (from-to)45-8
Number of pages4
JournalNeuroscience Letters
Volume271
Issue number1
Publication statusPublished - 13 Aug 1999

Keywords

  • Aged
  • Aged, 80 and over
  • Alzheimer Disease
  • Autopsy
  • Cell Cycle
  • Cell Nucleus
  • Cerebrovascular Disorders
  • Cyclin A
  • Cyclin B
  • Cyclin B1
  • Cyclin D1
  • Cyclin E
  • Cyclins
  • Dementia, Vascular
  • Hippocampus
  • Humans
  • Neurons
  • Reference Values

Fingerprint

Dive into the research topics of 'Cell cycle-related protein expression in vascular dementia and Alzheimer's disease'. Together they form a unique fingerprint.

Cite this