Neuroprotective effects of estrogen against beta-amyloid toxicity are mediated by estrogen receptors in cultured neuronal cells

• Published in: Neuroscience letters 2001-04, Vol.302 (1), p.58-62
• Main Authors: Kim, Hee, Bang, Oh Young, Jung, Min Whan, Ha, Sang Duk, Hong, Hyun Seok, Huh, Kyoon, Kim, Seung Up, Mook-Jung, Inhee
• Format: Article
• Language: English
• Subjects: Alzheimer's disease; Amyloid beta-Peptides - antagonists & inhibitors; Amyloid beta-Peptides - pharmacology; Apoptosis; Apoptosis - drug effects; Apoptosis - physiology; Beta amyloid; Biological and medical sciences; Cell death; Cell Death - drug effects; Cell Death - physiology; Cells, Cultured; Estradiol - analogs & derivatives; Estradiol - pharmacology; Estrogen; Estrogen Antagonists - pharmacology; Estrogen receptor; Estrogen Receptor alpha; Estrogen Receptor beta; Estrogens - pharmacology; Fulvestrant; Humans; Medical sciences; Neurons - drug effects; Neurons - metabolism; Neuropharmacology; Neuroprotective agent; Pharmacology. Drug treatments; Receptors, Estrogen - drug effects; Receptors, Estrogen - metabolism; Transfection
• ISSN: 0304-3940; 1872-7972
• DOI: 10.1016/S0304-3940(01)01659-7

Although estrogen is known to exert beneficial effects on Alzheimer's disease, its underlying cellular mechanisms have not been clear. In this study we investigated whether or not neuroprotective effects of estrogen are mediated by estrogen receptors (ERs). Treatment of estrogen (1.8 nM) reduced beta-amyloid (Aβ)-induced death of ER-expressing W4 cells. This effect of estrogen was blocked by a specific ER blocker ICI 182,780. When estrogen was treated to HT22 cells, which lack functional ERs, Aβ-induced cell death was not affected. Transfection of HT22 cells with human ERα, but not ERβ, restored protective action of estrogen against Aβ. Hoechst staining revealed that estrogen protected ERα-expressing cells by blocking Aβ-induced apoptosis. These results indicate that estrogen blocks Aβ-induced cell death via ERα-dependent pathways.