Estrogen receptors α and β in choroid plexus epithelial cells in Alzheimer's disease

Benecia C. Hong-Goka, Fen Lei F. Chang

Research output: Contribution to journalArticle

22 Scopus citations

Abstract

Estrogen replacement therapy (ERT) may reduce the risks of Alzheimer's disease (AD). One of the potential actions of estrogen is through its effect on β-amyloid elimination into the cerebrospinal fluid (CSF) compartment from the brain parenchyma. CSF secretion is controlled largely by the choroid plexus (CP) epithelial cells. In this study, we evaluated the status of estrogen receptor (ER) α and β subtypes in CP epithelial cells. Tissue from 49 AD and 12 non-AD patients were studied using immunohistochemistry with anti-ER antibodies. ER α and ER β were present in CP epithelial cells in both cytosolic and nuclear compartments. Male and female AD patients had lower ER α and β densities in CP compared to non-AD patients. We further stratified the female AD patients into four groups according to their hormonal status. Among the female AD patients, those without hysterectomy and with ERT had the highest ER α density. In contrast, those with hysterectomy and without ERT had the lowest ER α density. The effects of hysterectomy and ERT were additive. For ER β, ERT but not the status of hysterectomy was associated with higher receptor density. The lower ER density in CP epithelial cells of AD patients supports a potential role of estrogen in the regulation of CSF secretion of β-amyloid protein, which may affect the accumulation of β-amyloid in the brain parenchyma. Among AD patients, the association of ER α density with status of hysterectomy and ERT supports estrogen effects through receptor-mediated mechanisms.

Original languageEnglish (US)
Pages (from-to)113-116
Number of pages4
JournalNeuroscience Letters
Volume360
Issue number3
DOIs
StatePublished - Apr 29 2004

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Keywords

  • β-Amyloid
  • Alzheimer's disease
  • Cerebrospinal fluid
  • Choroid plexus
  • Estrogen receptor
  • Estrogen replacement
  • Hysterectomy

ASJC Scopus subject areas

  • Neuroscience(all)

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