Jo Misung, Brännström Mats, Akins James W, Curry Thomas E
Department of Obstetrics and Gynecology, University of Kentucky College of Medicine, Lexington, KY, USA.
Department of Obstetrics and Gynecology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Hum Reprod Update. 2025 Jan 1;31(1):21-47. doi: 10.1093/humupd/dmae027.
Successful ovulation is essential for natural conception and fertility. Defects in the ovulatory process are associated with various conditions of infertility or subfertility in women. However, our understanding of the intra-ovarian biochemical mechanisms underlying this process in women has lagged compared to our understanding of animal models. This has been largely due to the limited availability of human ovarian samples that can be used to examine changes across the ovulatory period and delineate the underlying cellular/molecular mechanisms in women. Despite this challenge, steady progress has been made to improve our knowledge of the ovulatory process in women by: (i) collecting granulosa cells across the IVF interval, (ii) creating a novel approach to collecting follicular cells and tissues across the periovulatory period from normally cycling women, and (iii) developing unique in vitro models to examine the LH surge or hCG administration-induced ovulatory changes in gene expression, the regulatory mechanisms underlying the ovulatory changes, and the specific functions of the ovulatory factors.
The objective of this review is to summarize findings generated using in vivo and in vitro models of human ovulation, with the goal of providing new insights into the mechanisms underlying the ovulatory process in women.
This review is based on the authors' own studies and a search of the relevant literature on human ovulation to date using PubMed search terms such as 'human ovulation EGF-signaling', 'human ovulation steroidogenesis', 'human ovulation transcription factor', 'human ovulation prostaglandin', 'human ovulation proteinase', 'human ovulation angiogenesis' 'human ovulation chemokine', 'human ovulatory disorder', 'human granulosa cell culture'. Our approach includes comparing the data from the authors' studies with the existing microarray or RNA-seq datasets generated using ovarian cells obtained throughout the ovulatory period from humans, monkeys, and mice.
Current findings from studies using in vivo and in vitro models demonstrate that the LH surge or hCG administration increases the expression of ovulatory mediators, including EGF-like factors, steroids, transcription factors, prostaglandins, proteolytic systems, and other autocrine and paracrine factors, similar to those observed in other animal models such as rodents, ruminants, and monkeys. However, the specific ovulatory factors induced, their expression pattern, and their regulatory mechanisms vary among different species. These species-specific differences stress the necessity of utilizing human samples to delineate the mechanisms underlying the ovulatory process in women.
The data from human ovulation in vivo and in vitro models have begun to fill the gaps in our understanding of the ovulatory process in women. Further efforts are needed to discover novel ovulatory factors. One approach to address these gaps is to improve existing in vitro models to more closely mimic in vivo ovulatory conditions in humans. This is critically important as the knowledge obtained from these human studies can be translated directly to aid in the diagnosis of ovulation-associated pathological conditions, for the development of more effective treatment to help women with anovulatory infertility or, conversely, to better manage ovulation for contraceptive purposes.
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成功排卵是自然受孕和生育的关键。排卵过程中的缺陷与女性的各种不孕或生育力低下状况相关。然而,与我们对动物模型的了解相比,我们对女性这一过程背后的卵巢内生化机制的认识较为滞后。这主要是由于可用于研究女性排卵周期变化并阐明其潜在细胞/分子机制的人类卵巢样本有限。尽管存在这一挑战,但通过以下方式在增进我们对女性排卵过程的认识方面取得了稳步进展:(i)在体外受精周期内收集颗粒细胞;(ii)创建一种从正常月经周期女性的围排卵期收集卵泡细胞和组织的新方法;(iii)开发独特的体外模型,以研究促黄体生成素激增或人绒毛膜促性腺激素给药诱导的排卵相关基因表达变化、排卵变化的调控机制以及排卵因子的特定功能。
本综述的目的是总结使用人类排卵的体内和体外模型所产生的研究结果,以期为女性排卵过程的潜在机制提供新见解。
本综述基于作者自身的研究以及使用诸如“人类排卵表皮生长因子信号传导”“人类排卵类固醇生成”“人类排卵转录因子”“人类排卵前列腺素”“人类排卵蛋白酶”“人类排卵血管生成”“人类排卵趋化因子”“人类排卵障碍”“人类颗粒细胞培养”等PubMed检索词对迄今为止关于人类排卵的相关文献进行的检索。我们的方法包括将作者研究的数据与使用从人类、猴子和小鼠整个排卵期获得的卵巢细胞生成的现有微阵列或RNA测序数据集进行比较。
使用体内和体外模型的当前研究结果表明,促黄体生成素激增或人绒毛膜促性腺激素给药会增加排卵介质的表达,包括表皮生长因子样因子、类固醇、转录因子、前列腺素、蛋白水解系统以及其他自分泌和旁分泌因子,这与在啮齿动物、反刍动物和猴子等其他动物模型中观察到的情况类似。然而,不同物种诱导的特定排卵因子、其表达模式及其调控机制各不相同。这些物种特异性差异强调了利用人类样本阐明女性排卵过程潜在机制的必要性。
来自人类排卵体内和体外模型的数据已开始填补我们对女性排卵过程认识上的空白。还需要进一步努力发现新的排卵因子。解决这些空白的一种方法是改进现有的体外模型,使其更紧密地模拟人类体内的排卵条件。这至关重要,因为从这些人类研究中获得的知识可直接转化,以帮助诊断与排卵相关的病理状况,开发更有效的治疗方法来帮助患有无排卵性不孕的女性,或者相反,更好地控制排卵以达到避孕目的。
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