Division of Endocrinology, Brigham and Women’s Hospital and Harvard Medical School, Boston, Massachusetts 02115, USA.
Endocrinology. 2012 Oct;153(10):4883-93. doi: 10.1210/en.2012-1529. Epub 2012 Aug 14.
At puberty, neurokinin B (NKB) and kisspeptin (Kiss1) may help to amplify GnRH secretion, but their precise roles remain ambiguous. We tested the hypothesis that NKB and Kiss1 are induced as a function of pubertal development, independently of the prevailing sex steroid milieu. We found that levels of Kiss1 mRNA in the arcuate nucleus (ARC) are increased prior to the age of puberty in GnRH/sex steroid-deficient hpg mice, yet levels of Kiss1 mRNA in wild-type mice remained constant, suggesting that sex steroids exert a negative feedback effect on Kiss1 expression early in development and across puberty. In contrast, levels of Tac2 mRNA, encoding NKB, and its receptor (NK3R; encoded by Tacr3) increased as a function of puberty in both wild-type and hpg mice, suggesting that during development Tac2 is less sensitive to sex steroid-dependent negative feedback than Kiss1. To compare the relative responsiveness of Tac2 and Kiss1 to the negative feedback effects of gonadal steroids, we examined the effect of estradiol (E(2)) on Tac2 and Kiss1 mRNA and found that Kiss1 gene expression was more sensitive than Tac2 to E(2)-induced inhibition at both juvenile and adult ages. This differential estrogen sensitivity was tested in vivo by the administration of E(2). Low levels of E(2) significantly suppressed Kiss1 expression in the ARC, whereas Tac2 suppression required higher E(2) levels, supporting differential sensitivity to E(2). Finally, to determine whether inhibition of NKB/NK3R signaling would block the onset of puberty, we administered an NK3R antagonist to prepubertal (before postnatal d 30) females and found no effect on markers of pubertal onset in either WT or hpg mice. These results indicate that the expression of Tac2 and Tacr3 in the ARC are markers of pubertal activation but that increased NKB/NK3R signaling alone is insufficient to trigger the onset of puberty in the mouse.
在青春期,神经激肽 B(NKB)和 kisspeptin(Kiss1)可能有助于放大 GnRH 分泌,但它们的确切作用仍不清楚。我们检验了这样一个假设,即 NKB 和 Kiss1 的表达是作为青春期发育的一个功能而被诱导的,独立于流行的性激素环境。我们发现,在 GnRH/性激素缺乏的 hpg 小鼠中,弓状核(ARC)中的 Kiss1 mRNA 水平在青春期前增加,而在野生型小鼠中,Kiss1 mRNA 水平保持不变,这表明性激素在发育早期和整个青春期对 Kiss1 表达产生负反馈作用。相比之下,编码 NKB 的 Tac2 mRNA 及其受体(由 Tacr3 编码)的水平随着野生型和 hpg 小鼠的青春期而增加,这表明在发育过程中,Tac2 对性激素依赖性负反馈的敏感性低于 Kiss1。为了比较 Tac2 和 Kiss1 对性腺类固醇负反馈作用的相对反应性,我们检查了雌激素(E2)对 Tac2 和 Kiss1 mRNA 的影响,发现 Kiss1 基因表达比 Tac2 对 E2 诱导的抑制更为敏感,无论是在青少年期还是成年期。这种差异的雌激素敏感性在体内通过给予 E2 进行了测试。低水平的 E2 显著抑制了 ARC 中的 Kiss1 表达,而 Tac2 的抑制需要更高水平的 E2,这支持了对 E2 的敏感性差异。最后,为了确定抑制 NKB/NK3R 信号是否会阻止青春期的开始,我们向青春期前(出生后第 30 天之前)的雌性小鼠给予 NK3R 拮抗剂,发现无论是在 WT 还是 hpg 小鼠中,对青春期开始的标志物都没有影响。这些结果表明,ARC 中 Tac2 和 Tacr3 的表达是青春期激活的标志物,但仅增加 NKB/NK3R 信号不足以触发小鼠青春期的开始。