Desaulniers Amy T, Cederberg Rebecca A, Mills Ginger A, Ford J Joe, Lents Clay A, White Brett R
University of Nebraska- Lincoln, Department of Animal Science, Lincoln, Nebraska.
US Department of Agriculture, Agricultural Research Service, U.S. Meat Animal Research Center, Clay Center, Nebraska.
Biol Reprod. 2015 Aug;93(2):45. doi: 10.1095/biolreprod.115.128082. Epub 2015 Jul 1.
Unlike classic gonadotropin-releasing hormone 1 (GNRH1), the second mammalian isoform (GNRH2) is an ineffective stimulant of gonadotropin release. Species that produce GNRH2 may not maintain a functional GNRH2 receptor (GNRHR2) due to coding errors. A full-length GNRHR2 gene has been identified in swine, but its role in reproduction requires further elucidation. Our objective was to examine the role of GNRH2 and GNRHR2 in testicular function of boars. We discovered that GNRH2 levels were higher in the testis than in the anterior pituitary gland or hypothalamus, corresponding to greater GNRHR2 abundance in the testis versus the anterior pituitary gland. Moreover, GNRH2 immunostaining was most prevalent within seminiferous tubules, whereas GNRHR2 was detected in high abundance on Leydig cells. GNRH2 pretreatment of testis explant cultures elicited testosterone secretion similar to that of human chorionic gonadotropin stimulation. Treatment of mature boars with GNRH2 elevated testosterone levels similar to those of GNRH1-treated males, despite minimal GNRH2-induced release of luteinizing hormone (LH). When pretreated with a GNRHR1 antagonist (SB-75), subsequent GNRH2 treatment stimulated low levels of testosterone secretion despite a pattern of LH release similar to that in the previous trial, suggesting that SB-75 inhibited testicular GNRHR2s. Given that pigs lack testicular GNRHR1, these data may indicate that GNRH2 and its receptor are involved in autocrine or paracrine regulation of testosterone secretion. Notably, our data are the first to suggest a biological function of a novel GNRH2-GNRHR2 system in the testes of swine.
与经典的促性腺激素释放激素1(GNRH1)不同,哺乳动物的第二种同种型(GNRH2)是促性腺激素释放的无效刺激物。由于编码错误,产生GNRH2的物种可能无法维持功能性的GNRH2受体(GNRHR2)。在猪中已鉴定出全长GNRHR2基因,但其在生殖中的作用需要进一步阐明。我们的目的是研究GNRH2和GNRHR2在公猪睾丸功能中的作用。我们发现,睾丸中的GNRH2水平高于垂体前叶或下丘脑,这与睾丸中GNRHR2的丰度高于垂体前叶相对应。此外,GNRH2免疫染色在生精小管中最为普遍,而GNRHR2在睾丸间质细胞中大量存在。对睾丸外植体培养物进行GNRH2预处理可引发与人类绒毛膜促性腺激素刺激相似的睾酮分泌。用GNRH2处理成年公猪可使睾酮水平升高,与用GNRH1处理的雄性相似,尽管GNRH2诱导的促黄体生成素(LH)释放极少。当用GNRHR1拮抗剂(SB - 75)预处理后,随后的GNRH2处理尽管LH释放模式与前一试验相似,但仍刺激了低水平的睾酮分泌,这表明SB - 75抑制了睾丸中的GNRHR2。鉴于猪缺乏睾丸GNRHR1,这些数据可能表明GNRH2及其受体参与了睾酮分泌的自分泌或旁分泌调节。值得注意的是,我们的数据首次表明了新型GNRH2 - GNRHR2系统在猪睾丸中的生物学功能。