Nguyen Dieu Thao, Archer Hannah, Earle Angel, Petyak Eleanor, Collins Carson, Vaillant Kayla, Lanford Hayes, Roudebush William E, Chang T Arthur, Kordus Rich, Green Lisa, Clay-Gilmour Alyssa, Chosed Renee J
Department of Biomedical Sciences, University of South Carolina School of Medicine Greenville, 607 Grove Rd., Greenville, SC, 29605, USA.
Department of Epidemiology and Biostatistics, University of South Carolina Arnold School of Public Health, Columbia, SC, USA.
J Assist Reprod Genet. 2025 Apr 22. doi: 10.1007/s10815-025-03485-7.
This retrospective study measured global gene abundance using RNASeq of blastocoel fluid-conditioned media from euploid ICSI-generated embryos to identify genes and signaling pathways associated with maternal age.
Blastocoel fluid-conditioned media was obtained following trophectoderm biopsy of ICSI-generated day-5 blastocysts. Media for RNASeq were from 24 euploid blastocysts (9 from patients aged 35 or older). Transcriptome analysis identified differentially expressed genes when comparing media from patients of advanced maternal age to those younger than 35. Further gene abundance analysis on genes and pathways identified from the RNASeq analysis was conducted with another group of media samples using RT-qPCR.
Twenty-five protein encoding genes identified in the RNASeq study were differentially expressed when comparing blastocoel fluid-conditioned media associated with patients of advanced maternal age to media associated with patients under the age of 35. Genes encoding the proteins SHARPIN and BCL2L12 showed a statistically significant increase (p < 0.05) in abundance in patients of advanced maternal age. Abundance analysis using RT-qPCR in additional media samples revealed elevated SHARPIN abundance in media associated with successful implantation in patients under 35 alongside a decrease in CASP8 abundance. This abundance pattern was the opposite in media associated with successful implantation in patients of advanced maternal age.
This study uncovered differential apoptotic gene abundance associated with maternal age by assessing blastocoel fluid-conditioned media from euploid blastocysts. These unique abundance patterns may provide insight into the regulation of apoptosis in embryos from women of advanced maternal age, and how this signaling pathway may impact implantation outcomes.
本回顾性研究使用来自整倍体ICSI生成胚胎的囊胚腔液条件培养基的RNA测序来测量全球基因丰度,以鉴定与母亲年龄相关的基因和信号通路。
在对ICSI生成的第5天囊胚进行滋养外胚层活检后获得囊胚腔液条件培养基。用于RNA测序的培养基来自24个整倍体囊胚(9个来自35岁及以上患者)。转录组分析在比较高龄产妇患者的培养基与35岁以下患者的培养基时鉴定出差异表达基因。使用另一组培养基样本通过RT-qPCR对从RNA测序分析中鉴定出的基因和通路进行进一步的基因丰度分析。
在比较与高龄产妇患者相关的囊胚腔液条件培养基和与35岁以下患者相关的培养基时,RNA测序研究中鉴定出的25个蛋白质编码基因差异表达。编码SHARPIN和BCL2L12蛋白的基因在高龄产妇患者中的丰度有统计学显著增加(p<0.05)。在额外的培养基样本中使用RT-qPCR进行的丰度分析显示,35岁以下患者中与成功着床相关的培养基中SHARPIN丰度升高,同时CASP8丰度降低。在高龄产妇患者中与成功着床相关的培养基中,这种丰度模式相反。
本研究通过评估来自整倍体囊胚的囊胚腔液条件培养基,发现了与母亲年龄相关的差异凋亡基因丰度。这些独特的丰度模式可能有助于深入了解高龄产妇胚胎中细胞凋亡的调控,以及这种信号通路如何影响着床结果。