Smith Jeremy T, Cunningham Matthew J, Rissman Emilie F, Clifton Donald K, Steiner Robert A
Department of Physiology and Biophysics, Health Sciences Building, G-424, School of Medicine, University of Washington, Box 357290, Seattle, Washington 98195-7290, USA.
Endocrinology. 2005 Sep;146(9):3686-92. doi: 10.1210/en.2005-0488. Epub 2005 May 26.
The Kiss1 gene encodes a family of neuropeptides called kisspeptins, which activate the receptor G protein-coupled receptor-54 and play a role in the neuroendocrine regulation of GnRH secretion. We examined whether estradiol (E2) regulates KiSS-1 in the forebrain of the female mouse by comparing KiSS-1 mRNA expression among groups of ovary-intact (diestrus), ovariectomized (OVX), and OVX plus E2-treated mice. In the arcuate nucleus (Arc), KiSS-1 expression increased after ovariectomy and decreased with E2 treatment. Conversely, in the anteroventral periventricular nucleus (AVPV), KiSS-1 expression was reduced after ovariectomy and increased with E2 treatment. To determine whether the effects of E2 on KiSS-1 are mediated through estrogen receptor (ER)alpha or ERbeta, we evaluated the effects of E2 in OVX mice that lacked functional ERalpha or ERbeta. In OVX mice that lacked functional ERalpha, KiSS-1 mRNA did not respond to E2 in either the Arc or AVPV, suggesting that ERalpha is essential for mediating the inhibitory and stimulatory effects of E2. In contrast, KiSS-1 mRNA in OVX mice that lacked functional ERbeta responded to E2 exactly as wild-type animals. Double-label in situ hybridization revealed that virtually all KiSS-1-expressing neurons in the Arc and AVPV coexpress ERalpha, suggesting that the effects of E2 are mediated directly through KiSS-1 neurons. We conclude that KiSS-1 neurons in the Arc, which are inhibited by E2, may play a role in the negative feedback regulation of GnRH secretion, whereas KiSS-1 neurons in the AVPV, which are stimulated by E2, may participate in the positive feedback regulation of GnRH secretion.
Kiss1基因编码一类名为亲吻素的神经肽,这些神经肽可激活G蛋白偶联受体54,并在促性腺激素释放激素(GnRH)分泌的神经内分泌调节中发挥作用。我们通过比较卵巢完整(动情间期)、卵巢切除(OVX)和OVX加雌二醇(E2)处理的小鼠组之间的KiSS-1 mRNA表达,研究了雌二醇(E2)是否调节雌性小鼠前脑的KiSS-1。在弓状核(Arc)中,卵巢切除后KiSS-1表达增加,而E2处理后表达降低。相反,在腹前室周核(AVPV)中,卵巢切除后KiSS-1表达降低,而E2处理后表达增加。为了确定E2对KiSS-1的影响是否通过雌激素受体(ER)α或ERβ介导,我们评估了E2对缺乏功能性ERα或ERβ的OVX小鼠的影响。在缺乏功能性ERα的OVX小鼠中,Arc或AVPV中的KiSS-1 mRNA对E2均无反应,这表明ERα对于介导E2的抑制和刺激作用至关重要。相比之下,缺乏功能性ERβ的OVX小鼠中的KiSS-1 mRNA对E2的反应与野生型动物完全相同。双标原位杂交显示,Arc和AVPV中几乎所有表达KiSS-1的神经元都共表达ERα,这表明E2的作用是直接通过KiSS-1神经元介导的。我们得出结论,Arc中受E2抑制的KiSS-1神经元可能在GnRH分泌的负反馈调节中发挥作用,而AVPV中受E2刺激的KiSS-1神经元可能参与GnRH分泌的正反馈调节。