Cooke Paul S, Nanjappa Manjunatha K, Ko CheMyong, Prins Gail S, Hess Rex A
Department of Physiological Sciences, University of Florida, Gainesville, Florida; Department of Comparative Biosciences, University of Illinois at Urbana-Champaign, Urbana, Illinois; Department of Urology, College of Medicine, University of Illinois at Chicago, Chicago, Illinois.
Physiol Rev. 2017 Jul 1;97(3):995-1043. doi: 10.1152/physrev.00018.2016.
Estrogens have historically been associated with female reproduction, but work over the last two decades established that estrogens and their main nuclear receptors (ESR1 and ESR2) and G protein-coupled estrogen receptor (GPER) also regulate male reproductive and nonreproductive organs. 17β-Estradiol (E2) is measureable in blood of men and males of other species, but in rete testis fluids, E2 reaches concentrations normally found only in females and in some species nanomolar concentrations of estrone sulfate are found in semen. Aromatase, which converts androgens to estrogens, is expressed in Leydig cells, seminiferous epithelium, and other male organs. Early studies showed E2 binding in numerous male tissues, and ESR1 and ESR2 each show unique distributions and actions in males. Exogenous estrogen treatment produced male reproductive pathologies in laboratory animals and men, especially during development, and studies with transgenic mice with compromised estrogen signaling demonstrated an E2 role in normal male physiology. Efferent ductules and epididymal functions are dependent on estrogen signaling through ESR1, whose loss impaired ion transport and water reabsorption, resulting in abnormal sperm. Loss of ESR1 or aromatase also produces effects on nonreproductive targets such as brain, adipose, skeletal muscle, bone, cardiovascular, and immune tissues. Expression of GPER is extensive in male tracts, suggesting a possible role for E2 signaling through this receptor in male reproduction. Recent evidence also indicates that membrane ESR1 has critical roles in male reproduction. Thus estrogens are important physiological regulators in males, and future studies may reveal additional roles for estrogen signaling in various target tissues.
雌激素在历史上一直与女性生殖相关联,但过去二十年的研究表明,雌激素及其主要核受体(ESR1和ESR2)以及G蛋白偶联雌激素受体(GPER)也对男性生殖和非生殖器官发挥调节作用。在男性及其他物种雄性个体的血液中可检测到17β - 雌二醇(E2),但在睾丸网液中,E2的浓度达到了通常仅在雌性个体中才有的水平,并且在某些物种的精液中还发现了纳摩尔浓度的硫酸雌酮。将雄激素转化为雌激素的芳香化酶在睾丸间质细胞、生精上皮及其他男性器官中均有表达。早期研究显示E2在众多男性组织中存在结合现象,并且ESR1和ESR2在雄性个体中各自呈现出独特的分布和作用。外源性雌激素处理在实验动物和男性中引发了雄性生殖病理变化,尤其是在发育过程中,而对雌激素信号传导受损的转基因小鼠的研究表明E2在正常雄性生理中发挥作用。输出小管和附睾功能依赖于通过ESR1的雌激素信号传导,ESR1缺失会损害离子转运和水重吸收,导致精子异常。ESR1或芳香化酶的缺失也会对非生殖靶器官产生影响,如脑、脂肪、骨骼肌、骨骼、心血管和免疫组织。GPER在男性生殖道中的表达广泛,提示通过该受体的E2信号传导在雄性生殖中可能发挥作用。最近的证据还表明膜ESR1在雄性生殖中具有关键作用。因此,雌激素是男性重要的生理调节因子,未来的研究可能会揭示雌激素信号传导在各种靶组织中的更多作用。