James L. Winkle College of Pharmacy, University of Cincinnati, Cincinnati, Ohio, USA.
Am J Physiol Regul Integr Comp Physiol. 2011 Sep;301(3):R746-56. doi: 10.1152/ajpregu.00138.2011. Epub 2011 Jun 8.
Prolactin (PRL), synthesized and secreted from lactotrophs of the anterior pituitary gland, is tonically inhibited by hypothalamic dopamine (DA) throughout the female reproductive (estrous) cycle. Our laboratory has shown that DA hyperpolarizes these cells by activating G protein-coupled inwardly rectifying K(+) (GIRK) channels; however, this response is only observed on proestrus. While the cellular mechanisms that allow for functional expression of this unique DA-signaling pathway are unclear, we hypothesized that activation of the DA-GIRK effector pathway is due to the rise in circulating estrogen (E₂) during the preceding day of diestrus. Thus, we examined the effects of E₂ on primary lactotrophs isolated from female rats. Treatment with a physiological concentration of E₂ (40-80 pg/ml, in vivo or in vitro) induced a proestrous phenotype in diestrous lactotrophs. These cells exhibited a DA-induced membrane hyperpolarization, as well as a secretory rebound of PRL following DA withdrawal (characteristic of proestrous cells). Internal dialysis of GTPγS demonstrated that E₂ exposure enabled functional expression of GIRK channels, and this regulation by E₂ did not involve the D₂R. The effect of E₂ was blocked by the receptor antagonist, ICI 182,780, and by the protein synthesis inhibitor, cycloheximide. Single-cell analysis revealed increased mRNA expression of GIRK channel subunits in E₂-treated lactotrophs. While E₂ is known to have multiple actions on the lactotroph, the present findings illuminate a novel action of E₂ in lactotrophs-regulation of the expression of a DA effector, the GIRK channel.
催乳素 (PRL) 是由垂体前叶的泌乳细胞合成和分泌的,在整个雌性生殖(发情)周期中受到下丘脑多巴胺 (DA) 的张力抑制。我们的实验室已经表明,DA 通过激活 G 蛋白偶联内向整流钾 (GIRK) 通道使这些细胞超极化;然而,这种反应仅在发情前期观察到。虽然允许表达这种独特的 DA 信号通路的细胞机制尚不清楚,但我们假设激活 DA-GIRK 效应途径是由于发情前期前一天循环雌激素 (E₂) 的增加。因此,我们检查了 E₂ 对从雌性大鼠分离的原代泌乳细胞的影响。用生理浓度的 E₂(体内或体外 40-80pg/ml)处理可诱导发情前期的发情期泌乳细胞表现出发情前期表型。这些细胞表现出 DA 诱导的膜超极化,以及 DA 撤出后 PRL 的分泌反弹(发情前期细胞的特征)。GTPγS 的内部透析表明,E₂ 暴露使 GIRK 通道的功能表达成为可能,而这种 E₂ 调节不涉及 D₂R。E₂ 的作用被受体拮抗剂 ICI 182,780 和蛋白质合成抑制剂环己酰亚胺阻断。单细胞分析显示,E₂ 处理的泌乳细胞中 GIRK 通道亚基的 mRNA 表达增加。虽然已知 E₂ 对泌乳细胞有多种作用,但目前的发现阐明了 E₂ 在泌乳细胞中的一种新作用——调节 DA 效应器 GIRK 通道的表达。