Visualisation and characterisation of oestrogen receptor α‐positive neurons expressing green fluorescent protein under the control of the oestrogen receptor α promoter. Issue 2 (19th April 2013)

• Record Type: Journal Article
• Authors: Matsuda, Ken Ichi; Yanagisawa, Miho; Sano, Kazuhiro; Ochiai, Ikuo; Musatov, Sergei; Okoshi, Kota; Tsukahara, Shinji; Ogawa, Sonoko; Kawata, Mitsuhiro
• Is Part Of: European journal of neuroscience. Volume 38:Issue 2(2013:Jul.)
• Page Start: 2242
• Page End: 2249
• Publication Date: 2013-04-19
• Subjects: Nervous system -- Periodicals; 612.8
• DOI: 10.1111/ejn.12227
• Languages: English
• ISSNs: 0953-816X

Abstract

<abstract abstract-type="main" id="ejn12227-abs-0001"> <title>Abstract</title> <p>Oestrogen receptor (ER)α plays important roles in the development and function of various neuronal systems through activation by its ligands, oestrogens. To visualise ERα‐positive neurons, we generated transgenic (tg) mice expressing green fluorescent protein (GFP) under the control of the ERα promoter. In three independent tg lines, GFP‐positive neurons were observed in areas previously reported to express ERα mRNA, including the lateral septum, bed nucleus of the stria terminalis, medial preoptic nucleus (MPO), hypothalamus, and amygdala. In these areas, GFP signals mostly overlapped with ERα immunoreactivity. GFP fluorescence was seen in neurites and cell bodies of neurons. In addition, the network and detailed structure of neurites were visible in dissociated and slice cultures of hypothalamic neurons. We examined the effect of oestrogen deprivation by ovariectomy on the structure of the GFP‐positive neurons. The area of ERα‐positive cell bodies in the bed nucleus of the stria terminalis and MPO was measured by capturing the GFP signal and was found to be significantly smaller in ovariectomy mice than in control mice. When neurons in the MPO were infected with an adeno‐associated virus that expressed small hairpin RNA targeting the ERα gene, an apparent induction of GFP was observed in this area, suggesting a negative feedback mechanism in which ERα controls expression of the ERα gene itself. Thus, the ERα promoter–GFP tg mice will be useful to analyse the development and plastic changes of the structure of ERα‐expressing neurons and oestrogen and its receptor‐mediated neuronal responses.</p> </abstract>