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膜定位雌激素受体1对小鼠正常雄性生殖发育和功能是必需的。

Membrane-Localized Estrogen Receptor 1 Is Required for Normal Male Reproductive Development and Function in Mice.

作者信息

Nanjappa Manjunatha K, Hess Rex A, Medrano Theresa I, Locker Seth H, Levin Ellis R, Cooke Paul S

机构信息

Department of Physiological Sciences (M.K.N., T.I.M., S.H.L., P.S.C.), University of Florida, Gainesville, Florida 32610; Department of Comparative Biosciences (R.A.H.), University of Illinois at Urbana-Champaign, Urbana, Illinois 61801; Division of Endocrinology (E.R.L.), Department of Medicine, University of California, Irvine, Irvine, California 92697; and Department of Veterans Affairs Medical Center (E.R.L.), Long Beach, Long Beach, California 90822.

出版信息

Endocrinology. 2016 Jul;157(7):2909-19. doi: 10.1210/en.2016-1085. Epub 2016 May 4.

Abstract

Estrogen receptor 1 (ESR1) mediates major reproductive functions of 17β-estradiol (E2). Male Esr1 knockout (Esr1KO) mice are infertile due to efferent ductule and epididymal abnormalities. The majority of ESR1 is nuclear/cytoplasmic; however, a small fraction is palmitoylated at cysteine 451 in mice and localized to cell membranes, in which it mediates rapid E2 actions. This study used an Esr1 knock-in mouse containing an altered palmitoylation site (C451A) in ESR1 that prevented cell membrane localization, although nuclear ESR1 was expressed. These nuclear-only estrogen receptor 1 (NOER) mice were used to determine the roles of membrane ESR1 in males. Epididymal sperm motility was reduced 85% in 8-month-old NOER mice compared with wild-type controls. The NOER mice had decreased epididymal sperm viability and greater than 95% of sperm had abnormalities, including coiled midpieces and tails, absent heads, and folded tails; this was comparable to 4-month Esr1KO males. At 8 months, daily sperm production in NOER males was reduced 62% compared with controls. The NOER mice had histological changes in the rete testes, efferent ductules, and seminiferous tubules that were comparable with those previously observed in Esr1KO males. Serum T was increased in NOER males, but FSH, LH, and E2 were unchanged. Critically, NOER males were initially subfertile, becoming infertile with advancing age. These findings identify a previously unknown role for membrane ESR1 in the development of normal sperm and providing an adequate environment for spermatogenesis.

摘要

雌激素受体1(ESR1)介导17β-雌二醇(E2)的主要生殖功能。雄性Esr1基因敲除(Esr1KO)小鼠由于输出小管和附睾异常而不育。ESR1大部分位于细胞核/细胞质中;然而,一小部分在小鼠的半胱氨酸451处发生棕榈酰化并定位于细胞膜,在细胞膜中它介导E2的快速作用。本研究使用了一种Esr1基因敲入小鼠,其ESR1中含有一个改变的棕榈酰化位点(C451A),该位点阻止了细胞膜定位,尽管细胞核ESR1仍有表达。这些仅含细胞核雌激素受体1(NOER)小鼠被用于确定膜ESR1在雄性中的作用。与野生型对照相比,8月龄NOER小鼠的附睾精子活力降低了85%。NOER小鼠的附睾精子活力下降,超过95%的精子存在异常,包括中段和尾部卷曲、无头、尾部折叠;这与4月龄的Esr1KO雄性小鼠相当。8个月时,NOER雄性小鼠的每日精子生成量比对照组减少了62%。NOER小鼠的睾丸网、输出小管和生精小管出现了组织学变化,与之前在Esr1KO雄性小鼠中观察到的变化相当。NOER雄性小鼠的血清睾酮升高,但促卵泡生成素、促黄体生成素和E2不变。至关重要的是,NOER雄性小鼠最初是亚不育的,随着年龄增长会变得不育。这些发现确定了膜ESR1在正常精子发育以及为精子发生提供适宜环境方面的一个此前未知的作用。

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