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黄体生成素通过牛卵巢膜旁旁分泌信号促进腔前卵泡的成熟和存活。

Luteinizing Hormone Facilitates Antral Follicular Maturation and Survival via Thecal Paracrine Signaling in Cattle.

机构信息

Department of Obstetrics and Gynecology, University of Fukui, Fukui, Japan.

Department of Obstetrics and Gynecology, Japanese Red Cross Fukui Hospital, Fukui, Japan.

出版信息

Endocrinology. 2018 Jun 1;159(6):2337-2347. doi: 10.1210/en.2018-00123.

Abstract

LH supplementation in assisted reproductive technology cycles improves the ongoing pregnancy rate in women with poor ovarian response (POR). However, our knowledge of the precise role of LH during the follicular phase of the menstrual cycle is incomplete. To explore the role of LH in the maturation of small antral follicles, we used an in vitro two-cell system that involved coculturing bovine granulosa cells (GCs) and theca cells (TCs) on a collagen membrane. Treatment of TCs with LH stimulated androgen production in TCs by inducing the expression of androgenic factors, subsequently increasing estrogen biosynthesis in GCs by providing androgen substrates, and inducing aromatase expression. LH stimulation of TCs induced functional LH receptor expression in GCs, a response modulated by the synthesis and action of estrogen. In the presence of TCs, LH stimulation of TCs and FSH stimulation of GCs increased the expression of IGF-1, IGF-2, and IGF-1 receptor in GCs. LH-induced expression of thecal IGF-1 protected GCs from apoptosis and promoted GC survival. Furthermore, LH stimulation of TCs increased FSH sensitivity in GCs. Thus, the LH-TC axis may be involved in the acquisition of LH dependence and the survival of small antral follicles by upregulating androgen/estrogen biosynthesis and activating the IGF system. The use of LH supplementation in ovarian stimulation may increase gonadotropin sensitivity in small antral follicles and promote follicular growth and survival by suppressing GC apoptosis and follicular atresia, resulting in multiple follicular development, even in patients with POR.

摘要

黄体生成素(LH)在辅助生殖技术周期中的补充可以提高卵巢反应不良(POR)女性的持续妊娠率。然而,我们对 LH 在月经周期卵泡期的确切作用的了解并不完整。为了探索 LH 在小窦卵泡成熟过程中的作用,我们使用了一种体外两细胞系统,该系统涉及在胶原膜上共培养牛颗粒细胞(GCs)和膜细胞(TCs)。用 LH 处理 TCs 会通过诱导雄激素因子的表达来刺激 TCs 产生雄激素,随后通过提供雄激素底物增加 GCs 中的雌激素生物合成,并诱导芳香酶表达。LH 对 TCs 的刺激会诱导 GCs 中功能性 LH 受体的表达,这一反应受到雌激素合成和作用的调节。在 TCs 的存在下,LH 对 TCs 的刺激和 FSH 对 GCs 的刺激增加了 GCs 中 IGF-1、IGF-2 和 IGF-1 受体的表达。LH 诱导的 TCs 中 IGF-1 的表达保护 GCs 免于凋亡并促进 GC 存活。此外,LH 对 TCs 的刺激增加了 GCs 对 FSH 的敏感性。因此,LH-TC 轴可能通过上调雄激素/雌激素生物合成和激活 IGF 系统来参与获得 LH 依赖性和小窦卵泡的存活。在卵巢刺激中使用 LH 补充可能会通过抑制 GC 凋亡和卵泡闭锁来增加小窦卵泡对促性腺激素的敏感性,并促进卵泡生长和存活,从而导致多个卵泡发育,即使是在 POR 患者中也是如此。

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