Estrogen up-regulates estrogen receptor α and synaptophysin in slice cultures of rat hippocampus

• Published in: Neuroscience 2002-01, Vol.113 (1), p.167-175
• Main Authors: Rune, G.M, Wehrenberg, U, Prange-Kiel, J, Zhou, L, Adelmann, G, Frotscher, M
• Format: Article
• Language: English
• Subjects: Animals; Biochemistry and metabolism; Biological and medical sciences; Blotting, Western; Central nervous system; Culture Techniques; Estrogen Receptor alpha; Estrogen Receptor beta; Estrogens - metabolism; Estrogens - pharmacology; Fundamental and applied biological sciences. Psychology; hippocampal circuitry; Hippocampus - drug effects; Hippocampus - metabolism; Immunohistochemistry; In Situ Hybridization; Interneurons - metabolism; Pyramidal Cells - metabolism; Rats; Rats, Inbred Lew; Receptors, Estrogen - drug effects; Receptors, Estrogen - genetics; Receptors, Estrogen - metabolism; RNA, Messenger - metabolism; Schaffer collaterals; slice culture; steroid receptor; synaptic plasticity; synaptogenesis; Synaptophysin - drug effects; Synaptophysin - immunology; Synaptophysin - metabolism; Up-Regulation - drug effects; Vertebrates: nervous system and sense organs
• ISSN: 0306-4522; 1873-7544
• DOI: 10.1016/S0306-4522(02)00152-5

Previous studies have shown that estrogen application increases the density of synaptic input and the number of spines on CA1 pyramidal neurons. Here, we have investigated whether Schaffer collaterals to CA1 pyramidal cells are involved in this estrogen-induced synaptogenesis on CA1 pyramidal neurons. To this end, we studied estrogen-induced expression of both estrogen receptor (ER) subtypes (ERα and ERβ) together with the presynaptic marker synaptophysin in the rat hippocampus. In tissue sections as well as in slice cultures mRNA expression of ERα, ERβ and synaptophysin was higher in CA3 than in CA1, and mRNA expression and immunoreactivity for both ER subtypes were found in both principal cells and interneurons. By using quantitative image analysis we found stronger nuclear immunoreactivity for ERα in CA3 than in CA1. In slice cultures, supplementation of the medium with 10 −8 M estradiol led to an increase of nuclear immunoreactivity for ERα, but not for ERβ, which was accompanied by a dramatic up-regulation of synaptophysin immunoreactivity in stratum radiatum of CA1. Together these findings indicate that estrogen effects on hippocampal neurons are more pronounced in CA3 than in CA1 and that ER activation in CA3 neurons leads to an up-regulation of a presynaptic marker protein in the axons of these cells, the Schaffer collaterals. We conclude that estradiol-induced spine formation on CA1 pyramidal cells may be mediated presynaptically, very likely by activation of ERα in CA3 pyramidal cells, followed by an increase in Schaffer collateral synapses.