Ozaki Saeko, Higo Shimpei, Iwata Kinuyo, Saeki Hidehisa, Ozawa Hitoshi
Department of Anatomy and Neurobiology, Graduate School of Medicine, Nippon Medical School, Sendagi 1-1-5, Bunkyo-ku, Tokyo, 113-8602, Japan.
Department of Dermatology, Graduate School of Medicine, Nippon Medical School, Tokyo, Japan.
Histochem Cell Biol. 2019 Jul;152(1):25-34. doi: 10.1007/s00418-018-01767-z. Epub 2019 Jan 22.
Kisspeptin acts as a potent neuropeptide regulator of reproduction through modulation of the hypothalamic-pituitary-gonadal axis. Previous studies revealed sex differences in brain expression patterns as well as regulation of expression by estrogen. Alternatively, sex differences and estrogen regulation of the kisspeptin receptor (encoded by Kiss1r) have not been examined at cellular resolution. In the current study, we examined whether Kiss1r mRNA expression also exhibits estrogen sensitivity and sex-dependent differences using in situ hybridization. We compared Kiss1r mRNA expression between ovariectomized (OVX) rats and estradiol (E2)-replenished OVX rats to examine estrogen sensitivity, and compared expression between gonadally intact male rats and female rats in diestrus or proestrus to examine sex differences. In OVX rats, E2 replenishment significantly reduced Kiss1r expression specifically in the hypothalamic arcuate nucleus (ARC). A difference in Kiss1r expression was also observed between diestrus and proestrus rats in the hypothalamic paraventricular nucleus (PVN), but not in the ARC. Thus, estrogen appears to have region- and context-specific effects on Kiss1r expression. However, immunostaining revealed minimal colocalization of estrogen receptor alpha (ERα) in Kiss1r-expressing neuronal populations of ARC and PVN, indicating indirect or ERα-independent regulation of Kiss1r expression. Surprisingly, unlike the kisspeptin ligand, no sexual dimorphisms were observed in either the brain distribution of Kiss1r expression or in the number of Kiss1r-expressing neurons within enriched brain nuclei. The current study reveals marked differences in regulation between kisspeptin and kisspeptin receptor, and provides an essential foundation for further study of kisspeptin signaling and function in reproduction.
亲吻素通过调节下丘脑 - 垂体 - 性腺轴,作为一种强大的生殖神经肽调节剂。先前的研究揭示了大脑表达模式的性别差异以及雌激素对表达的调节作用。另外,亲吻素受体(由Kiss1r编码)的性别差异和雌激素调节尚未在细胞分辨率水平上进行研究。在本研究中,我们使用原位杂交技术研究了Kiss1r mRNA表达是否也表现出雌激素敏感性和性别依赖性差异。我们比较了去卵巢(OVX)大鼠和补充雌二醇(E2)的OVX大鼠之间的Kiss1r mRNA表达,以检查雌激素敏感性,并比较性腺完整的雄性大鼠与处于动情间期或动情前期的雌性大鼠之间的表达,以检查性别差异。在OVX大鼠中,E2补充显著降低了下丘脑弓状核(ARC)中Kiss1r的表达。在下丘脑室旁核(PVN)中,动情间期和动情前期大鼠之间也观察到Kiss1r表达的差异,但在ARC中未观察到。因此,雌激素似乎对Kiss1r表达具有区域和背景特异性影响。然而,免疫染色显示雌激素受体α(ERα)在ARC和PVN中表达Kiss1r的神经元群体中的共定位极少,表明Kiss1r表达存在间接或不依赖于ERα的调节。令人惊讶的是,与亲吻素配体不同,在Kiss1r表达的脑部分布或富含脑核内表达Kiss1r的神经元数量方面均未观察到性二态性。本研究揭示了亲吻素与亲吻素受体在调节方面的显著差异,并为进一步研究亲吻素信号传导及其在生殖中的功能提供了重要基础。