Affiliations: [a] Neuroscience Program, Michigan State University, East Lansing, MI 48824, USA | [b] Department of Physiology, Michigan State University, East Lansing, MI 48824, USA | [c] Department of Microbiology and Molecular Genetics, Michigan State University, East Lansing, MI 48824, USA | [d] Department of Psychology, Michigan State University, East Lansing, MI 48824, USA
Correspondence:
[*]
Corresponding author: Cheryl L. Sisk, Neuroscience Program, Michigan State University, East Lansing, MI 48824, USA. Tel.: +1 517 355 5253; Fax: +1 517 432 2744; E-mail: sisk@msu.edu.
Abstract: Estrogen replacement therapy in postmenopausal women is associated with a reduced risk of Alzheimer's Disease (AD). The multiple mechanisms by which estrogen protects against AD are still unknown. To conduct a broad screen for estrogen-regulated AD-related genes in the brain, we used cDNA array assays of brain mRNA samples from ovariectomized (ovx) adult female mice treated with either 17β-estradiol or vehicle at 1 or 5 weeks post-ovx. The gene encoding transthyretin (TTR), which has been reported to scavenge amyloid β peptides and reduce amyloid plaque formation, is increased by estradiol treatment at both 1 and 5 weeks post-ovx. Northern blot analyses and RNase protection assays performed on whole brain samples obtained from estradiol- or vehicle-treated mice confirmed the cDNA array assays showing a significant increase in TTR mRNA with estradiol treatment. Qualitative in situ hybridization or immunocytochemistry performed on brain sections demonstrated that TTR mRNA is expressed only in choroid plexus and leptomeninges, and that both estrogen receptor proteins, α and β, are present in choroid plexus cells. These novel findings suggest that estrogen may reduce the risk of AD by acting on choroid plexus cells to increase TTR gene expression, leading to enhanced sequestration and reduced aggregation of amyloid β peptides.
