Pinceti E, Shults C L, Rao Y S, Mott N N, Pak T R
Department of Cell and Molecular Physiology, Loyola University Chicago, Stritch School of Medicine, Maywood, IL, USA.
J Neuroendocrinol. 2015 Dec;27(12):861-71. doi: 10.1111/jne.12326.
Nuclear steroid hormone receptors are ubiquitously expressed transcription factors whose activity can be altered by post-translational modifications, such as phosphorylation. The consequences of post-translational modifications have been described for several members of the nuclear steroid hormone receptor superfamily; however, little is known about the effects of oestrogen receptor (ER)β phosphorylation in the brain. Moreover, to our knowledge, the presence of phosphorylated ERβ has not been detected in the brain of any species to date. Oestrogen receptor β is highly expressed in several regions of the brain and in vitro studies have demonstrated that it can be phosphorylated at two serine residues (S87 and S105) in the N-terminal AF-1 region. The present study aimed to determine whether phosphorylated ERβ is detectable in the hippocampus of aged female rats, as well as the functional consequences of ERβ S87 and S105 phosphorylation on transcriptional activity in neuronal cells. First, we used a novel PhosTag(™) approach to detect phosphorylated forms of ERβ in the dorsal hippocampus of aged female rats. The data obtained demonstrated abundant forms of phosphorylated ERβ in the dorsal hippocampus, suggesting that this post-translational modification might be an important regulator of ERβ function. To assess the functional consequences of ERβ phosphorylation in neuronal cells, we created phospho-mimetic (S87E, S105E) and phospho-null (S87A, S105A) ERβ receptors that were transiently transfected in a hippocampal-derived cell line. Collectively, our results showed that phosphorylation of S87 and S105 altered both ligand-independent and ligand-dependent ERβ transcriptional regulation. Overall, these data demonstrate that phosphorylated forms of ERβ are present in the brain of aged female rats and that phosphorylation of ERβ could differentially alter ERβ-mediated gene expression.
核类固醇激素受体是普遍表达的转录因子,其活性可通过翻译后修饰(如磷酸化)而改变。核类固醇激素受体超家族的几个成员的翻译后修饰后果已被描述;然而,关于雌激素受体(ER)β磷酸化在大脑中的作用知之甚少。此外,据我们所知,迄今为止在任何物种的大脑中都未检测到磷酸化的ERβ。雌激素受体β在大脑的几个区域高度表达,体外研究表明它可以在N端AF-1区域的两个丝氨酸残基(S87和S105)处被磷酸化。本研究旨在确定在老年雌性大鼠的海马体中是否可检测到磷酸化的ERβ,以及ERβ S87和S105磷酸化对神经元细胞转录活性的功能影响。首先,我们使用一种新颖的PhosTag(™)方法来检测老年雌性大鼠背侧海马体中ERβ的磷酸化形式。获得的数据表明背侧海马体中存在丰富形式的磷酸化ERβ,这表明这种翻译后修饰可能是ERβ功能的重要调节因子。为了评估ERβ磷酸化在神经元细胞中的功能影响,我们构建了磷酸模拟(S87E、S105E)和磷酸缺失(S87A、S105A)的ERβ受体,并将其瞬时转染到海马来源的细胞系中。总的来说,我们的结果表明S87和S105的磷酸化改变了ERβ的非配体依赖性和配体依赖性转录调控。总体而言,这些数据表明磷酸化形式的ERβ存在于老年雌性大鼠的大脑中,并且ERβ的磷酸化可以不同程度地改变ERβ介导的基因表达。