Department of Physiology, Centre for Neuroendocrinology, School of Medical Sciences, University of Otago, Dunedin, New Zealand.
J Neuroendocrinol. 2012 Jun;24(6):907-15. doi: 10.1111/j.1365-2826.2012.02294.x.
Kisspeptin and its G-protein coupled receptor Gpr54 are essential for the pubertal activation of gonadotrophin-releasing hormone (GnRH) neurones, with Gpr54 mutation or deletion resulting in failed puberty and infertility in humans and mice. The number of kisspeptin-immunoreactive neurones in the rostral periventricular area of the third ventricle (RP3V) increases during pubertal development in concert with the appearance of kisspeptin appositions with GnRH neurones in the mouse rostral preoptic area. We recently demonstrated that the pubertal increase in RP3V kisspeptin neuronal number in females is dependent upon circulating oestradiol levels. The present experiments investigated the potential role of gonadal steroids in the induction of kisspeptin expression in the RP3V during pubertal development in the male mouse. Using immunocytochemistry (ICC), we show that gonadectomy of male pups at postnatal day (P) 20 resulted in a 60-70% reduction in the number of kisspeptin immunoreactive (IR) neurones within the RP3V of P45 mice (P<0.05) compared to sham-treated littermates. We established a profile of circulating testosterone levels during postnatal development in male mice and found that circulating testosterone was low throughout early postnatal development and increased from P35-40 to reach adult levels. Treatment of P20-gonadectomised male mice with 17β-oestradiol or testosterone from P38-45 restored kisspeptin-IR neurone number in the RP3V to intact control levels (P>0.05). Using double-label ICC, we demonstrate that the majority of RP3V kisspeptin neurones express androgen receptors and oestrogen receptor α, indicating that RP3V kisspeptin neurones in the male mouse are equipped to respond to both androgen and oestrogen signals. These results indicate that, as in females, gonadal steroids are essential for the increase in kisspeptin immunoreactive cell number that occurs in the RP3V during pubertal development in the male mouse.
Kisspeptin 和其 G 蛋白偶联受体 Gpr54 对于促性腺激素释放激素 (GnRH) 神经元的青春期激活至关重要,Gpr54 突变或缺失会导致人类和小鼠青春期失败和不育。在青春期发育过程中,第三脑室(RP3V)前室周区的 kisspeptin 免疫反应神经元数量增加,同时伴随着小鼠前脑前区 kisspeptin 与 GnRH 神经元的 kisspeptin 吻合出现。我们最近证明,雌性 RP3V kisspeptin 神经元数量的青春期增加取决于循环雌激素水平。本实验研究了在雄性小鼠青春期发育过程中,生殖类固醇在 RP3V 中诱导 kisspeptin 表达的潜在作用。通过免疫细胞化学(ICC),我们发现,在出生后第 20 天(P)对雄性幼鼠进行性腺切除术,会导致 P45 小鼠的 RP3V 中的 kisspeptin 免疫反应(IR)神经元数量减少 60-70%(P<0.05),与假手术处理的同窝幼鼠相比。我们建立了雄性小鼠在出生后发育过程中循环睾酮水平的概况,发现循环睾酮在整个早期出生后发育过程中都很低,并从 P35-40 增加到成年水平。从 P38-45 开始用 17β-雌二醇或睾酮治疗 P20 性腺切除术雄性小鼠,可将 RP3V 中的 kisspeptin-IR 神经元数量恢复到完整对照水平(P>0.05)。通过双标记 ICC,我们证明大多数 RP3V kisspeptin 神经元表达雄激素受体和雌激素受体α,表明雄性小鼠的 RP3V kisspeptin 神经元有能力对雄激素和雌激素信号作出反应。这些结果表明,与雌性小鼠一样,生殖类固醇对于雄性小鼠青春期发育过程中 RP3V 中 kisspeptin 免疫反应细胞数量的增加是必不可少的。