卵巢FKBP51表达增强与卵巢衰老相关:女性年龄相关生育的分子洞察

Papri Sarkar, Monica Moore, Asli Ozmen, Busra Cetinkaya-Un, Julie Vitko, Anthony N Imudia, Charles J Lockwood, Umit A Kayisli, Ozlem Guzeloglu-Kayisli
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Lastly, this relation was further queried by comparing ovarian expression of several collagen genes as markers of ovarian fibrosis in 14-month-old wild type (Fkbp5<sup>+/+</sup>) and Fkbp5 knockout (Fkbp5<sup>-/-</sup>) mice.</p><p><strong>Design: </strong>Laboratory based experimental study.</p><p><strong>Setting: </strong>Academic-affiliated assisted reproductive technology unit/laboratory SUBJECTS: (1) Samples collected included follicular fluid (FF), CC, GC and serum from group 1: Young women with normal ovarian reserve (<35 years; n=12); group 2: DOR (anti-Mullerian hormone (AMH) <1 ng/mL; n=10); and group 3: Women of advanced age with normal ovarian reserve (>37 years; n=8). (2) Ovarian stromal tissues obtained from surgical specimen of post-menopausal (50-65 years; n=6) and pre-menopausal (18-30 years; n=6). 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Analysis of qPCR revelated that 1) Col1a1, Col1a2, Col3a1 levels were significantly lower in ovaries obtained from 14-month-old Fkbp5<sup>-/-</sup>vs. Fkbp5<sup>+/+</sup> mice; 2) FKBP5 levels significantly increased in cumulus cells of advanced age women vs. younger women (1.71± 0.22 vs. 1.11± 0.15, P= 0.03); and 3) FKBP5 levels were ∼3-fold higher in granulosa cells of women with DOR vs. age-matched control (3.22± 1.11 vs. 1.30± 0.54 P= 0.03).</p><p><strong>Conclusion: </strong>This study for the first time demonstrates expression profile of FKBP51 in human ovary and its potential role in ovarian aging. Our results indicate that the upregulation of FKBP51 is associated with ovarian aging. Moreover, in women undergoing IVF treatment, enhanced FKBP51 expression is seen in those with DOR or women of advanced maternal reproductive age, who have poor prognosis. 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引用次数: 0

摘要

目的:通过比较高龄和/或诊断为DOR的卵巢控制性刺激(COS)时收集的颗粒细胞(GC)和积云细胞(CC)中fk506结合蛋白51 (FKBP51)与卵巢储备功能正常的年轻女性的fk506结合蛋白51 (FKBP51)水平,研究fk506结合蛋白51与卵巢老化和/或卵巢储备功能减退(DOR)之间的关系。为了进一步探讨FKBP51表达升高与人类卵巢衰老的关系,我们比较了绝经后和绝经前女性卵巢间质中FKBP51的表达。最后,通过比较14月龄野生型(Fkbp5+/+)和Fkbp5敲除型(Fkbp5-/-)小鼠卵巢中几种胶原基因作为卵巢纤维化标志物的表达,进一步探究这种关系。设计:基于实验室的实验研究。背景:学术附属辅助生殖技术单位/实验室受试者:(1)收集的样本包括第1组的卵泡液(FF)、CC、GC和血清:卵巢储备正常的年轻女性(37岁;n = 8)。(2)绝经后(50 ~ 65岁)手术标本获得的卵巢间质组织;N =6)和绝经前(18-30岁;n = 6)。(3) Fkbp5+/+和Fkbp5-/-小鼠14月龄卵巢组织。暴露:比较FKBP51在COS妇女GC和CC、绝经前和绝经后妇女卵巢间质组织、老年Fkbp5+/+和Fkbp5-/-小鼠卵巢组织中的表达。主要观察指标:(1)人GC和CC中FKBP51的水平,通过RT-qPCR (RT-qPCR)在COS期间收集。(2)免疫组化(IHC)检测FKBP51水平,Picrosirius Red染色(PSR)检测人卵巢间质组织胶原沉积。(3) RT-qPCR比较Fkbp5+/+和Fkbp5-/-老年小鼠卵巢中几种胶原蛋白基因的表达水平。(4) ELISA法测定血清和FF中TGF-β1、可溶性内啡肽水平。结果:IHC显示绝经后妇女卵巢间质组织中FKBP51 HSCORE水平明显高于绝经前妇女(Mean±SEM;160.52±17.75 vs. 120.67±14.33,P= 0.002)。绝经后和绝经前妇女的小天狼星红染色较强,提示纤维化(54.06±6.94比37.50±14.29,P=0.02)。qPCR分析显示:1)14月龄Fkbp5-/-vs卵巢Col1a1、Col1a2、Col3a1水平显著降低。Fkbp5 + / +老鼠;2)老年女性积云细胞中FKBP5水平明显高于年轻女性(1.71±0.22比1.11±0.15,P= 0.03);3)与年龄匹配的对照组相比,DOR女性颗粒细胞中FKBP5水平高出约3倍(3.22±1.11比1.30±0.54 P= 0.03)。结论:本研究首次揭示了FKBP51在人卵巢中的表达谱及其在卵巢衰老中的潜在作用。我们的研究结果表明FKBP51的上调与卵巢衰老有关。此外,在接受IVF治疗的女性中,DOR患者或产妇生育年龄较晚且预后较差的女性中FKBP51表达增强。因此,靶向抑制FKBP51表达和/或活性的药物可能延缓卵巢衰老或治疗卵巢早衰。
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Enhanced Ovarian FKBP51 Expression is Associated with Ovarian Aging: A Molecular Insight for Age-Related Fertility in Women.

Objective: To study the relationship between FK506-binding protein 51 (FKBP51) and ovarian aging and/or diminished ovarian reserve (DOR) in human ovaries by comparing FKBP51 levels in granulosa (GC) and cumulus cells (CC), collected during controlled ovarian stimulation (COS) from women of advanced reproductive age and/or with a diagnosis of DOR with that of young women with normal ovarian reserve. To explore the association between increased FKBP51 expression and human ovarian aging further, expression of FKBP51 was compared in ovarian stroma of post-menopausal versus pre-menopausal women. Lastly, this relation was further queried by comparing ovarian expression of several collagen genes as markers of ovarian fibrosis in 14-month-old wild type (Fkbp5+/+) and Fkbp5 knockout (Fkbp5-/-) mice.

Design: Laboratory based experimental study.

Setting: Academic-affiliated assisted reproductive technology unit/laboratory SUBJECTS: (1) Samples collected included follicular fluid (FF), CC, GC and serum from group 1: Young women with normal ovarian reserve (<35 years; n=12); group 2: DOR (anti-Mullerian hormone (AMH) <1 ng/mL; n=10); and group 3: Women of advanced age with normal ovarian reserve (>37 years; n=8). (2) Ovarian stromal tissues obtained from surgical specimen of post-menopausal (50-65 years; n=6) and pre-menopausal (18-30 years; n=6). (3) 14-month-old ovarian tissues from Fkbp5+/+and Fkbp5-/- mice.

Exposure: Comparison of FKBP51 expression in GC and CC from women undergoing COS, ovarian stromal tissue from pre- and post-menopausal women, and ovarian tissue from aged Fkbp5+/+and Fkbp5-/- mice.

Main outcome measures: (1) Level of FKBP51 in human GC and CC, collected during COS by performing RT-quantitative PCR (RT-qPCR). (2) Immunohistochemistry (IHC) to detect FKBP51 levels and Picrosirius Red Staining (PSR) to detect collagen deposition in human ovarian stromal tissue. (3) RT-qPCR to compare expression levels of several collagen genes in Fkbp5+/+ and Fkbp5-/- old mice ovaries. (4) Serum and FF levels of TGF-β1, and soluble Endoglin measured by ELISA.

Results: IHC revealed that FKBP51 HSCORE levels in ovarian stromal tissue were significantly higher in post- vs. pre-menopausal women (Mean± SEM; 160.52±17.75 vs. 120.67±14.33, P= 0.002). Stronger Picrosirius Red staining, suggestive of fibrosis, was seen in post- vs. pre-menopausal women (54.06± 6.94 vs. 37.50± 14.29, P=0.02). Analysis of qPCR revelated that 1) Col1a1, Col1a2, Col3a1 levels were significantly lower in ovaries obtained from 14-month-old Fkbp5-/-vs. Fkbp5+/+ mice; 2) FKBP5 levels significantly increased in cumulus cells of advanced age women vs. younger women (1.71± 0.22 vs. 1.11± 0.15, P= 0.03); and 3) FKBP5 levels were ∼3-fold higher in granulosa cells of women with DOR vs. age-matched control (3.22± 1.11 vs. 1.30± 0.54 P= 0.03).

Conclusion: This study for the first time demonstrates expression profile of FKBP51 in human ovary and its potential role in ovarian aging. Our results indicate that the upregulation of FKBP51 is associated with ovarian aging. Moreover, in women undergoing IVF treatment, enhanced FKBP51 expression is seen in those with DOR or women of advanced maternal reproductive age, who have poor prognosis. Therefore, drugs targeting inhibition of FKBP51 expression and/or activity may delay ovarian aging or treat premature ovarian aging.

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来源期刊
F&S science
F&S science Endocrinology, Diabetes and Metabolism, Obstetrics, Gynecology and Women's Health, Urology
CiteScore
2.00
自引率
0.00%
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审稿时长
51 days
期刊最新文献
Enhanced Ovarian FKBP51 Expression is Associated with Ovarian Aging: A Molecular Insight for Age-Related Fertility in Women. Polycystic ovary syndrome and morphokinetic embryonic development: A case-control study evaluating 791 embryos. Chemotherapy-induced diminished murine ovarian reserve model and impact of low-dose chemotherapy on fertility. From the Editor-in-Chief. Luteinizing hormone receptor deficiency in immature cumulus-oocyte complexes retrieved for assisted reproduction.
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