Single-cell RNA sequencing identifies molecular targets associated with poor in vitro maturation performance of oocytes collected from ovarian stimulation.

细胞生物学 体外 卵泡发生 卵泡期 信使核糖核酸 分子生物学 胚泡 生发泡 卵子发生 体外受精 卵泡
作者
Annie Wing Tung Lee,Judy Kin Wing Ng,Jinyue Liao,Alfred Chun Shui Luk,Ashley Hoi Ching Suen,T T H Chan,M Y Cheung,H T Chu,Nelson L.S. Tang,Mingpeng Zhao,Q Lian,Wai-Yee Chan,David Yiu Leung Chan,Tak Yeung Leung,King Lau Chow,Wenjun Wang,L H Wang,N C H Chen,W J Yang,J Y Huang,Tin-Chiu Li,Tin-Lap Lee
出处
期刊:Human Reproduction [Oxford University Press]
卷期号:36 (7): 1907-1921 被引量:2
标识
DOI:10.1093/humrep/deab100
摘要

Study question What is the transcriptome signature associated with poor performance of rescue IVM (rIVM) oocytes and how can we rejuvenate them? Summary answer The GATA-1/CREB1/WNT signalling axis was repressed in rIVM oocytes, particularly those of poor quality; restoration of this axis may produce more usable rIVM oocytes. What is known already rIVM aims to produce mature oocytes (MII) for IVF through IVM of immature oocytes collected from stimulated ovaries. It is not popular due to limited success rate in infertility treatment. Genetic aberrations, cellular stress and the absence of cumulus cell support in oocytes could account for the failure of rIVM. Study design, size, duration We applied single-cell RNA sequencing (scRNA-seq) to capture the transcriptomes of human in vivo oocytes (IVO) (n = 10) from 7 donors and rIVM oocytes (n = 10) from 10 donors. The effects of maternal age and ovarian responses on rIVM oocyte transcriptomes were also studied. In parallel, we studied the effect of gallic acid on the maturation rate of mouse oocytes cultured in IVM medium with (n = 84) and without (n = 85) gallic acid. Participants/materials, setting, methods Human oocytes were collected from donors aged 28-41 years with a body mass index of Main results and the role of chance The transcriptome profiles of rIVM/IVO oocytes showed distinctive differences. A total of 1559 differentially expressed genes (DEGs, genes with at least 2-fold change and adjusted P Large scale data Raw data from this study can be accessed through GSE158539. Limitations, reasons for caution In the rIVM oocytes of the high- and low-quality comparison, the number of samples was limited after data filtering with stringent selection criteria. For the oocyte stage identification, we were unable to predict the presence of oocyte spindle, so polar body extrusion was the only indicator. Wider implications of the findings This study showed that GATA-1/CREB1/WNT signalling was repressed in rIVM oocytes compared with IVO oocytes and was further downregulated in low-quality rIVM oocytes, providing us the foundation of subsequent follow-up research on human oocytes and raising safety concerns about the clinical use of rescued oocytes. Study funding/competing interest(s) This work was supported by the Collaborative Research Fund, Research Grants Council, C4054-16G, and Research Committee Funding (Research Sustainability of Major RGC Funding Schemes), The Chinese University of Hong Kong. The authors have no conflicts of interest to declare.
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