Depletion of placental brain-derived neurotrophic factor (BDNF) is attributed to premature ovarian insufficiency (POI) in mice offspring.

IF 3.8 3区 医学 Q1 REPRODUCTIVE BIOLOGY
Bin Liu, Yongjie Liu, Shuman Li, Pingping Chen, Jun Zhang, Liping Feng
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Abstract

Introduction: Premature ovarian insufficiency (POI) is one of the causes of female infertility. Unexplained POI is increasingly affecting women in their reproductive years. However, the etiology of POI is diverse and remains elusive. We and others have shown that brain-derived neurotrophic factor (BDNF) plays an important role in adult ovarian function. Here, we report on a novel role of BDNF in the Developmental Origins of POI.

Methods: Placental BDNF knockout mice were created using CRISPR/CAS9. Homozygous knockout (cKO(HO)) mice didn't survive, while heterozygous knockout (cKO(HE)) mice did. BDNF reduction in cKO(HE) mice was confirmed via immunohistochemistry and Western blots. Ovaries were collected from cKO(HE) mice at various ages, analyzing ovarian metrics, FSH expression, and litter sizes. In one-month-old mice, oocyte numbers were assessed using super-ovulation, and oocyte gene expression was analyzed with smart RNAseq. Ovaries of P7 mice were studied with SEM, and gene expression was confirmed with RT-qPCR. Alkaline phosphatase staining at E11.5 and immunofluorescence for cyclinD1 assessed germ cell number and cell proliferation.

Results: cKO(HE) mice had decreased ovarian function and litter size in adulthood. They were insensitive to ovulation induction drugs manifested by lower oocyte release after superovulation in one-month-old cKO(HE) mice. The transcriptome and SEM results indicate that mitochondria-mediated cell death or aging might occur in cKO(HE) ovaries. Decreased placental BDNF led to diminished primordial germ cell proliferation at E11.5 and ovarian reserve which may underlie POI in adulthood.

Conclusion: The current results showed decreased placental BDNF diminished primordial germ cell proliferation in female fetuses during pregnancy and POI in adulthood. Our findings can provide insights into understanding the underlying mechanisms of POI.

胎盘脑源性神经营养因子(BDNF)的消耗是导致小鼠后代卵巢早衰(POI)的原因。
导言卵巢早衰(POI)是导致女性不孕的原因之一。不明原因的卵巢早衰越来越多地影响着育龄期女性。然而,POI 的病因多种多样,仍然难以捉摸。我们和其他人已经证明,脑源性神经营养因子(BDNF)在成人卵巢功能中发挥着重要作用。在此,我们报告了 BDNF 在 POI 发育起源中的新作用:方法:利用 CRISPR/CAS9 技术创建了胎盘 BDNF 基因敲除小鼠。同基因敲除(cKO(HO))小鼠无法存活,而杂基因敲除(cKO(HE))小鼠可以存活。免疫组化和 Western 印迹证实了 cKO(HE)小鼠中 BDNF 的减少。从不同年龄的cKO(HE)小鼠体内收集卵巢,分析卵巢指标、FSH表达和产仔数。在一个月大的小鼠中,使用超级排卵法评估卵母细胞数量,并使用智能 RNAseq 分析卵母细胞基因表达。用 SEM 对 P7 小鼠的卵巢进行研究,并用 RT-qPCR 确认基因表达。结果:cKO(HE)小鼠成年后卵巢功能下降,产仔数减少。结果:cKO(HE)小鼠成年后卵巢功能下降,产仔数减少,对促排卵药物不敏感,表现为一个月大的cKO(HE)小鼠超排卵后卵母细胞释放量减少。转录组和扫描电镜结果表明,线粒体介导的细胞死亡或衰老可能发生在cKO(HE)卵巢中。胎盘BDNF减少导致E11.5原始生殖细胞增殖和卵巢储备减少,这可能是成年后POI的原因:目前的研究结果表明,胎盘BDNF的降低会减少女性胎儿在妊娠期原始生殖细胞的增殖和成年后的POI。我们的研究结果有助于了解 POI 的内在机制。
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来源期刊
Journal of Ovarian Research
Journal of Ovarian Research REPRODUCTIVE BIOLOGY-
CiteScore
6.20
自引率
2.50%
发文量
125
审稿时长
>12 weeks
期刊介绍: Journal of Ovarian Research is an open access, peer reviewed, online journal that aims to provide a forum for high-quality basic and clinical research on ovarian function, abnormalities, and cancer. The journal focuses on research that provides new insights into ovarian functions as well as prevention and treatment of diseases afflicting the organ. Topical areas include, but are not restricted to: Ovary development, hormone secretion and regulation Follicle growth and ovulation Infertility and Polycystic ovarian syndrome Regulation of pituitary and other biological functions by ovarian hormones Ovarian cancer, its prevention, diagnosis and treatment Drug development and screening Role of stem cells in ovary development and function.
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