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通过表皮生长因子(EGF)处理在小鼠和人类体内及体外激活休眠原始卵泡。

In vivo and in vitro activation of dormant primordial follicles by EGF treatment in mouse and human.

作者信息

Zhang Jiawei, Yan Lei, Wang Yibo, Zhang Shuo, Xu Xueqiang, Dai Yanli, Zhao Shidou, Li Zhen, Zhang Yan, Xia Guoliang, Qin Yingying, Zhang Hua

机构信息

State Key Laboratory of Agrobiotechnology, College of Biological Sciences, China Agricultural University, Beijing, 100193, China.

Center for Reproductive Medicine, Shandong University, Jinan, 250021, China.

出版信息

Clin Transl Med. 2020 Sep;10(5):e182. doi: 10.1002/ctm2.182.

DOI:10.1002/ctm2.182
PMID:32997412
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7520080/
Abstract

In the mammalian ovaries, dormant primordial follicles represent the reproductive reserve of individual females. Recently, stimulating the activation of primordial follicles in vitro has been practiced, making the utilization of those dormant follicles to treat female infertility possible. However, there are still lacks of effective upstream molecule and strategy to elevate follicle activation in vivo. In the current study, we revealed that growth factor EGF improved a transiently primordial follicle activation in mice by elevating the CDC42-PI3K signaling activity, and EGF treatment also improved the activation and development of human follicles in ovarian cortical pieces. Using a liquid-solid phase transition bio-gel as a carrier, an efficient in vivo activation system was established by ovarian topical EGF administration to living mice. We found that EGF treatment led to an increase of primordial follicle activation in short time but had no effect on long-term fertility in females. By establishing an inducible premature ovarian insufficiency (POI) mouse model through selectively ablating growing follicles in Zp3-Cre;iDTR mice, we further revealed that our in vivo EGF treatment system improved primordial follicle activation and ovulation of POI ovaries significantly. Taken together, our results revealed that in situ ovarian EGF administration could improve the activation of primordial follicles in living animals, and manipulating activation and development of primordial follicles in vivo might be an efficient approach to improve reproductive health in women.

摘要

在哺乳动物卵巢中,静止的原始卵泡代表着个体雌性的生殖储备。近来,体外刺激原始卵泡激活的技术已得到应用,使得利用这些休眠卵泡治疗女性不孕症成为可能。然而,目前仍缺乏有效的上游分子和策略来提高体内卵泡的激活率。在本研究中,我们发现生长因子表皮生长因子(EGF)通过提高细胞分裂周期蛋白42(CDC42)-磷脂酰肌醇-3激酶(PI3K)信号活性,改善了小鼠体内原始卵泡的短暂激活,且EGF处理还促进了人卵巢皮质块中卵泡的激活和发育。通过将液-固相变生物凝胶作为载体,对活体小鼠进行卵巢局部EGF给药,建立了一种高效的体内激活系统。我们发现,EGF处理可在短时间内增加原始卵泡的激活,但对雌性小鼠的长期生育能力并无影响。通过在Zp3-Cre;iDTR小鼠中选择性消融生长卵泡,建立了一种诱导性卵巢早衰(POI)小鼠模型,我们进一步发现,我们的体内EGF治疗系统显著改善了POI卵巢的原始卵泡激活和排卵。综上所述,我们的结果表明,卵巢原位给予EGF可改善活体动物体内原始卵泡的激活,而调控体内原始卵泡的激活和发育可能是改善女性生殖健康的有效途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b956/7520080/c3d2cd69e2e7/CTM2-10-e182-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b956/7520080/0b0623edf758/CTM2-10-e182-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b956/7520080/169aef83abe5/CTM2-10-e182-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b956/7520080/10cd1233785c/CTM2-10-e182-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b956/7520080/308cf890157c/CTM2-10-e182-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b956/7520080/c3d2cd69e2e7/CTM2-10-e182-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b956/7520080/0b0623edf758/CTM2-10-e182-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b956/7520080/169aef83abe5/CTM2-10-e182-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b956/7520080/10cd1233785c/CTM2-10-e182-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b956/7520080/308cf890157c/CTM2-10-e182-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b956/7520080/c3d2cd69e2e7/CTM2-10-e182-g005.jpg

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BMC Biol. 2018 Jul 5;16(1):73. doi: 10.1186/s12915-018-0541-4.
3
The epidermal growth factor network: role in oocyte growth, maturation and developmental competence.
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Sleep Deprivation Triggers the Excessive Activation of Ovarian Primordial Follicles via β2 Adrenergic Receptor Signaling.睡眠剥夺通过β2 肾上腺素能受体信号触发卵巢原始卵泡的过度激活。
Adv Sci (Weinh). 2024 Nov;11(41):e2402393. doi: 10.1002/advs.202402393. Epub 2024 Sep 4.
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