Center for Alzheimer's and Neurodegenerative Disease Research and Center for Neuroscience Discovery, Institute for Healthy Aging, University of North Texas Health Science Center, Fort Worth, TX 76107.
eNeuro. 2017 Aug 29;4(4). doi: 10.1523/ENEURO.0109-17.2017. eCollection 2017 Jul-Aug.
Fast, nongenomic androgen actions have been described in various cell types, including neurons. However, the receptor mediating this cell membrane-initiated rapid signaling remains unknown. This study found a putative androgen receptor splice variant in a dopaminergic N27 cell line and in several brain regions (substantia nigra pars compacta, entorhinal cortex, and hippocampus) from gonadally intact and gonadectomized (young and middle-aged) male rats. This putative splice variant protein has a molecular weight of 45 kDa and lacks an N-terminal domain, indicating it is homologous to the human AR45 splice variant. Interestingly, AR45 was highly expressed in all brain regions examined. In dopaminergic neurons, AR45 is localized to plasma membrane lipid rafts, a microdomain involved in cellular signaling. Further, AR45 protein interacts with membrane-associated G proteins Gαq and Gαo. Neither age nor hormone levels altered AR45 expression in dopaminergic neurons. These results provide the first evidence of AR45 protein expression in the brain, specifically plasma membrane lipid rafts. AR45 presence in lipid rafts indicates that it may function as a membrane androgen receptor to mediate fast, nongenomic androgen actions.
快速的非基因组雄激素作用已在各种细胞类型中描述,包括神经元。然而,介导这种细胞膜起始的快速信号转导的受体仍然未知。本研究在多巴胺能 N27 细胞系和来自性腺完整和性腺切除(年轻和中年)雄性大鼠的几个脑区(黑质致密部、内嗅皮层和海马体)中发现了一种推定的雄激素受体剪接变体。这种推定的剪接变体蛋白的分子量为 45 kDa,缺乏 N 端结构域,表明它与人类 AR45 剪接变体同源。有趣的是,AR45 在所有检查的脑区都高度表达。在多巴胺能神经元中,AR45 定位于质膜脂筏,这是一个参与细胞信号转导的微区。此外,AR45 蛋白与膜相关 G 蛋白 Gαq 和 Gαo 相互作用。年龄和激素水平都没有改变多巴胺能神经元中的 AR45 表达。这些结果首次提供了 AR45 蛋白在大脑中,特别是在质膜脂筏中的表达证据。AR45 在脂筏中的存在表明,它可能作为膜雄激素受体发挥作用,介导快速的非基因组雄激素作用。