Horta Fabrizzio, Ravichandran Aravind, Catt Sally, Vollenhoven Beverley, Temple-Smith Peter
Education Program in Reproduction and Development, EPRD, Department of Obstetrics and Gynecology, School of Clinical Science, Monash University, Melbourne, VIC, 3168, Australia.
Monash IVF, Melbourne, VIC, 3168, Australia.
J Assist Reprod Genet. 2021 Jan;38(1):55-69. doi: 10.1007/s10815-020-01981-6. Epub 2020 Oct 17.
Oocyte quality and reproductive outcome are negatively affected by advanced maternal age, ovarian stimulation and method of oocyte maturation during assisted reproduction; however, the mechanisms responsible for these associations are not fully understood. The aim of this study was to compare the effects of ageing, ovarian stimulation and in-vitro maturation on the relative levels of transcript abundance of genes associated with DNA repair during the transition of germinal vesicle (GV) to metaphase II (MII) stages of oocyte development.
The relative levels of transcript abundance of 90 DNA repair-associated genes was compared in GV-stage and MII-stage oocytes from unstimulated and hormone-stimulated ovaries from young (5-8-week-old) and old (42-45-week-old) C57BL6 mice. Ovarian stimulation was conducted using pregnant mare serum gonadotropin (PMSG) or anti-inhibin serum (AIS). DNA damage response was quantified by immunolabeling of the phosphorylated histone variant H2AX (γH2AX).
The relative transcript abundance in DNA repair genes was significantly lower in MII oocytes compared to GV oocytes in young unstimulated and PMSG stimulated but was higher in AIS-stimulated mice. Interestingly, an increase in the relative level of transcript abundance of DNA repair genes was observed in MII oocytes from older mice in unstimulated, PMSG-stimulated and AIS-stimulated mice. Decreased γH2AX levels were found in both GV oocytes (82.9%) and MII oocytes (37.5%) during ageing in both ovarian stimulation types used (PMSG/AIS; p < 0.05).
In conclusion, DNA repair relative levels of transcript abundance are altered by maternal age and the method of ovarian stimulation during the GV-MII transition in oocytes.
在辅助生殖过程中,高龄产妇、卵巢刺激及卵母细胞成熟方法会对卵母细胞质量和生殖结局产生负面影响;然而,这些关联背后的机制尚未完全明确。本研究旨在比较衰老、卵巢刺激及体外成熟对卵母细胞从生发泡(GV)期向中期 II(MII)期发育转变过程中与 DNA 修复相关基因转录本丰度相对水平的影响。
比较了来自年轻(5 - 8 周龄)和年老(42 - 45 周龄)C57BL6 小鼠未受刺激和激素刺激卵巢的 GV 期和 MII 期卵母细胞中 90 个与 DNA 修复相关基因的转录本丰度相对水平。使用孕马血清促性腺激素(PMSG)或抗抑制素血清(AIS)进行卵巢刺激。通过对磷酸化组蛋白变体 H2AX(γH2AX)进行免疫标记来定量 DNA 损伤反应。
在未受刺激和 PMSG 刺激的年轻小鼠中,MII 期卵母细胞中 DNA 修复基因的相对转录本丰度显著低于 GV 期卵母细胞,但在 AIS 刺激的小鼠中则较高。有趣的是,在未受刺激、PMSG 刺激和 AIS 刺激的老年小鼠的 MII 期卵母细胞中,观察到 DNA 修复基因转录本丰度相对水平有所增加。在两种使用的卵巢刺激类型(PMSG/AIS)的衰老过程中,GV 期卵母细胞(82.9%)和 MII 期卵母细胞(37.5%)中均发现 γH2AX 水平降低(P < 0.05)。
总之,在卵母细胞从 GV 期向 MII 期转变过程中,母体年龄和卵巢刺激方法会改变 DNA 修复相关转录本丰度的相对水平。