Barreiro M L, Gaytán F, Caminos J E, Pinilla L, Casanueva F F, Aguilar E, Diéguez C, Tena-Sempere M
Department of Cell Biology, Physiology, and Immunology, University of Córdoba, Spain.
Biol Reprod. 2002 Dec;67(6):1768-76. doi: 10.1095/biolreprod.102.006965.
Ghrelin, the endogenous ligand for the growth hormone-secretagogue receptor, is a recently cloned 28-amino acid peptide, expressed primarily in the stomach and hypothalamus, with the ability to stimulate growth hormone (GH) release and food intake. However, the possibility of additional, as yet unknown biological actions of ghrelin has been suggested. As a continuation of our recent findings on the expression and functional role of ghrelin in rat testis, we report here the pattern of cellular expression of ghrelin peptide in rat testis during postnatal development and after selective Leydig cell elimination, and we assess hormonal regulation of testicular ghrelin expression, at the mRNA and/or protein levels, in different experimental models. Immunohistochemical analyses along postnatal development demonstrated selective location of ghrelin peptide within rat testis in mature fetal- and adult-type Leydig cells. In good agreement, ghrelin protein appeared undetectable in testicular interstitium after selective Leydig cell withdrawal. In terms of hormonal regulation, testicular ghrelin mRNA and protein expression decreased to negligible levels after long-term hypophysectomy, whereas replacement with human chorionic gonadotropin (CG) (as superagonist of LH) partially restored ghrelin mRNA and peptide expression. Furthermore, acute administration of human CG (25 IU) to intact rats resulted in a transient increase in testicular ghrelin mRNA levels, with peak values 4 h after injection, an effect that was not mimicked by FSH (12.5 IU/rat). In contrast, testicular expression of ghrelin mRNA remained unaltered in GH-deficient rats, under hyper- and hypothyroidism conditions, as well as in adrenalectomized animals. In conclusion, our results demonstrate that mature Leydig cells are the source of ghrelin expression in rat testis, the protein being expressed in both fetal- and adult-type Leydig cells. In addition, our data indicate that testicular expression of ghrelin is hormonally regulated and is at least partially dependent on pituitary LH.
胃饥饿素是生长激素促分泌素受体的内源性配体,是一种最近克隆出的含28个氨基酸的肽,主要在胃和下丘脑表达,具有刺激生长激素(GH)释放和食物摄入的能力。然而,胃饥饿素可能还存在其他尚未知晓的生物学作用。作为我们近期关于胃饥饿素在大鼠睾丸中的表达及功能作用研究的延续,我们在此报告出生后发育期间及选择性消除睾丸间质细胞后大鼠睾丸中胃饥饿素肽的细胞表达模式,并在不同实验模型中评估睾丸胃饥饿素表达在mRNA和/或蛋白质水平上的激素调节情况。出生后发育过程中的免疫组织化学分析表明,胃饥饿素肽在大鼠睾丸中选择性地定位于成熟胎儿型和成年型睾丸间质细胞。与此一致的是,选择性消除睾丸间质细胞后,在睾丸间质中未检测到胃饥饿素蛋白。在激素调节方面,长期垂体切除术后,睾丸胃饥饿素mRNA和蛋白表达降至可忽略不计的水平,而用人绒毛膜促性腺激素(CG)(作为促黄体生成素的超级激动剂)替代则部分恢复了胃饥饿素mRNA和肽的表达。此外,向完整大鼠急性注射人CG(25 IU)导致睾丸胃饥饿素mRNA水平短暂升高,注射后4小时达到峰值,促卵泡生成素(FSH)(12.5 IU/大鼠)未模拟出这种效应。相反,在生长激素缺乏的大鼠中,以及在甲状腺功能亢进和减退状态下以及肾上腺切除的动物中,睾丸胃饥饿素mRNA的表达保持不变。总之,我们的结果表明,成熟睾丸间质细胞是大鼠睾丸中胃饥饿素表达的来源,该蛋白在胎儿型和成年型睾丸间质细胞中均有表达。此外,我们的数据表明,睾丸胃饥饿素的表达受激素调节,并且至少部分依赖于垂体促黄体生成素。