Control of aromatase in hippocampal neurons

• Published in: The Journal of steroid biochemistry and molecular biology Vol. 160; pp. 9 - 14
• Main Authors: Fester, Lars, Brandt, Nicola, Windhorst, Sabine, Pröls, Felicitas, Bläute, Corinna, Rune, Gabriele M.
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 01.06.2016
• Subjects: 17β-Estradiol; Animals; Aromatase; Aromatase - metabolism; Aromatase immunohistochemistry; Aromatase phosphorylation; Ca2+ transients; Calcium - metabolism; Estradiol - metabolism; Hippocampus - cytology; Hippocampus - metabolism; Humans; Neurons; Neurons - cytology; Neurons - metabolism; Phosphorylation; 17β-Estradiol; Aromatase phosphorylation; Neurons; Ca2+ transients; Aromatase; Aromatase immunohistochemistry; Ca(+) transients
• ISSN: 0960-0760; 1879-1220
• DOI: 10.1016/j.jsbmb.2015.10.009

•Estradiol is synthesized in hippocampal neurons.•Aromatase in hippocampal neurons becomes phoshorylated upon treatment of the neurons with estradiol.•Estradiol release from hippocampal neurons is stimulated by depletion of Ca2+ stores using thapsigargin.•Aromatase protein is upregulated upon treatment of hippocampal neurons with estradiol. Our knowledge on estradiol-induced modulation of synaptic function in the hippocampus is widely based on results following the application of the steroid hormone to either cell cultures, or after the treatment of gonadectomized animals, thus ignoring local neuronal estrogen synthesis. We and others, however, have shown that hippocampus-derived estradiol also controls synaptic plasticity in the hippocampus. Estradiol synthesis in the hippocampus is regulated by several mechanisms, which are reviewed in this report. The regulation of the activity of aromatase, the final enzyme of estrogen biosynthesis, by Ca2+ transients, is of particular interest. Aromatase becomes inactivated as soon as it is phosphorylated by Ca2+-dependent kinases upon calcium release from internal stores. Accordingly, thapsigargin dephosphorylates aromatase and stimulates estradiol synthesis by depletion of internal Ca2+ stores. Vice versa, letrozole, an aromatase inhibitor, phosphorylates aromatase and reduces estradiol synthesis. Treatment of the cultures with 17β-estradiol results in phosphorylation of the enzyme and increased aromatase protein expression, which suggests that estradiol synthesis in hippocampal neurons is regulated in an autocrine manner.