4.5 Article

Rats Display Sexual Dimorphism in Phosphorylation of Brain Tau with Age

期刊

JOURNAL OF ALZHEIMERS DISEASE
卷 82, 期 2, 页码 855-869

出版社

IOS PRESS
DOI: 10.3233/JAD-210341

关键词

Alzheimer's disease; entorhinal cortex; gender; hippocampus; protein phosphorylation; tau expression; tau iso-forms

资金

  1. New York State Office for People with Developmental Disabilities
  2. Alzheimer's Association [2016-NIRG-397030]

向作者/读者索取更多资源

The study revealed that male and female rats have comparable levels of total tau, 3R-tau, and 4R-tau, but females exhibit higher levels of tau phosphorylated at multiple sites, potentially underlying the gender disparity in brain tau burden and risk for AD.
Background: Women have a two-fold higher risk than men to Alzheimer's disease (AD) at midlife. Larger brain tau burden was consistently shown in older women than age-matched men. The biological basis for this gender disparity remains elusive. Objective: We sought to knowwhether tau expression and phosphorylation physiologically differ between males and females. Methods: We used western blots and immunohistochemistry to compare the levels of total tau and phosphorylated tau in the hippocampus and entorhinal cortex (EC) between sexes in Wistar rats at 40 days, and 8 and 20 months of age. Results: We detected no statistically significant difference in total tau, 3R-tau, and 4R-tau between sexes. However, female rats exhibited lower levels of tau unphosphorylated at the Tau-1 site at 40 days of age. At 8 months of age, females showed higher levels of tau phosphorylated at Ser(190), Ser(387), and Ser(395) (Ser(199), Ser(396), and Ser(404) of human tau, respectively) than males in EC. At 20 months of age, both brain regions of female rats consistently showed higher levels than males of tau phosphorylated at Ser(253), Ser(387), PHF-1 (Ser(387/395)), and Ser(413) sites, which correspond to Ser(262), Ser(396), Ser(396/404), and Ser(422) of human tau, respectively. Conclusion: Rats of both sexes have comparable levels of total tau, 3R-tau, and 4R-tau, whereas females exhibit higher levels of tau phosphorylated at multiple sites that are implicated in AD tau pathology, indicating a sexual dimorphism of tau phosphorylation that may potentially underlie the disparity in brain tau burden and risk for AD between sexes.

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