Ingram Asia, Kumar T Rajendra
Integrated Physiology Graduate Program, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Division of Reproductive Sciences, Department of Obstetrics and Gynecology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Andrology. 2025 Jul 11. doi: 10.1111/andr.70094.
Gonadotropins are synthesized in gonadotropes of the anterior pituitary, and they orchestrate reproductive function in vertebrates. LH and FSH share a common α-subunit that is non-covalently associated with a hormone - and receptor-specific β-subunit. Despite synthesized in the same cell, i.e., gonadotrope the trafficking and secretion patterns of LH and FSH are distinct. FSH is mostly constitutively secreted, whereas LH is stored in dense core granules and is released as a bolus via the regulated pathway in response to gonadotropin-releasing hormone.
To comparatively review the storage and secretion patterns of gonadotropins in vertebrates.
Gonadotropin storage patterns are comparatively analyzed in vertebrates starting from primitive fish all the way up to higher mammals. The published work on gonadotropin trafficking/secretion patterns using in vitro and in vivo approaches is critically discussed.
Primitive fish (lampreys and hagfish) express a single gonadotropic hormone. From these early vertebrates, luteinizing hormone (LH) and follicle-stimulating hormone (FSH) have evolved as two distinct hormones. In several species, including teleost fish, monohormonal gonadotropes are present that express either LH or FSH. In higher vertebrates, the majority of the gonadotropes (>90%) are bihormonal and contain both LH and FSH. Both in vitro (cell transfection and expression) and in vivo (transgenic mouse) studies identified that the LHβ caroboxy terminus heptapeptide is a gonadotrope-specific regulated pathway sorting determinant.
When FSH is genetically rerouted from the constitutive trafficking mode and is engineered (LHβ heptapeptide fused to FSHβ subunit) to exit via the regulated pathway in gonadotropes of transgenic mice, it resulted in enhanced ovulations due to suppression of atresia and apoptosis and increased pro-survival pathways in ovaries. However, rerouted FSH expressing male mice did not demonstrate any gain of function phenotypes.
Understanding the basic molecular mechanisms of gonadotropin storage/trafficking and secretion may eventually lead to clinical benefits of enhancing female reproductive function and reproductive lifespan.
促性腺激素由垂体前叶的促性腺细胞合成,在脊椎动物中协调生殖功能。促黄体生成素(LH)和促卵泡生成素(FSH)共享一个与激素和受体特异性β亚基非共价结合的共同α亚基。尽管LH和FSH在同一细胞即促性腺细胞中合成,但其运输和分泌模式却不同。FSH大多组成性分泌,而LH则储存于致密核心颗粒中,并通过受调节的途径以脉冲形式释放,以响应促性腺激素释放激素。
比较综述脊椎动物中促性腺激素的储存和分泌模式。
对从原始鱼类到高等哺乳动物的脊椎动物促性腺激素储存模式进行比较分析。对已发表的使用体外和体内方法研究促性腺激素运输/分泌模式的工作进行批判性讨论。
原始鱼类(七鳃鳗和盲鳗)表达单一促性腺激素。从这些早期脊椎动物开始,促黄体生成素(LH)和促卵泡生成素(FSH)逐渐演变为两种不同的激素。在包括硬骨鱼在内的几个物种中,存在表达LH或FSH的单激素促性腺细胞。在高等脊椎动物中,大多数促性腺细胞(>90%)是双激素的,同时含有LH和FSH。体外(细胞转染和表达)和体内(转基因小鼠)研究均表明,LHβ羧基末端七肽是促性腺细胞特异性受调节途径分选决定因素。
当FSH通过基因改造从组成性运输模式转变为经工程改造(将LHβ七肽与FSHβ亚基融合)后,通过转基因小鼠促性腺细胞的受调节途径分泌时,由于抑制闭锁和凋亡以及增加卵巢中的促存活途径,导致排卵增加。然而,表达经改造FSH的雄性小鼠未表现出任何功能增强的表型。
了解促性腺激素储存/运输和分泌的基本分子机制最终可能带来增强女性生殖功能和延长生殖寿命的临床益处。