EUGIN Group, Research and Development, Parc Científic de Barcelona, Barcelona, Spain.
Department of Genetics, Microbiology and Statistic, CIBERER, IBUB, IRSJD, Universitat de Barcelona, Barcelona, Spain.
Mol Reprod Dev. 2023 Jun;90(6):369-377. doi: 10.1002/mrd.23698. Epub 2023 Jul 24.
Throughout the reproductive life of women, cumulus cells (CC) protect the dormant oocyte from damage, act as sensors of the follicular microenvironment, and act as a gatekeeper for oocyte developmental potential. One such mechanism relies on the hypoxia-tolerance response, which, with age, decreases systematically, including in the ovary. We aimed to evaluate the association between gene expression related to hypoxia and aging in CC and reproductive results in in vitro fertilization cycles. We recruited 94 women undergoing controlled ovarian stimulation. Total RNA was extracted from pooled CCs collected after oocyte pick-up (OPU) and reverse-transcribed to complementary DNA using random hexamers to test 14 genes related to hypoxia response via HIF1α activation, oxidative stress, and angiogenic responses. The expression of CLU, NOS2, and TXNIP had a positive correlation with age (r = 0.25, r = 0.24, and r = 0.35, respectively). Additionally, NOS2 and HMOX1 expression correlated positively with the retrieval of immature oocytes (r = 0.22 and r = 0.40, respectively). Moreover, VEGFC levels decreased overall with increasing fertilization rate, independently of age (r = -0.29). We found that the fertilization potential of a cohort of oocytes is related to the ability of CC to respond to oxidative stress and hypoxia with age, pointing at NOS2, HMOX1, and VEGFC expression as markers for oocyte maturation and fertilization success.
在女性的生殖生命周期中,卵丘细胞 (CC) 保护休眠卵母细胞免受损伤,充当卵泡微环境的传感器,并充当卵母细胞发育潜能的守门员。其中一种机制依赖于耐缺氧反应,随着年龄的增长,这种反应会系统性地下降,包括在卵巢中。我们旨在评估 CC 中与缺氧和衰老相关的基因表达与体外受精周期中的生殖结果之间的关联。我们招募了 94 名接受控制性卵巢刺激的女性。在卵母细胞采集 (OPU) 后从汇集的 CC 中提取总 RNA,并使用随机六聚体将其逆转录为 cDNA,以通过 HIF1α 激活、氧化应激和血管生成反应测试与缺氧反应相关的 14 个基因的表达。CLU、NOS2 和 TXNIP 的表达与年龄呈正相关(r 分别为 0.25、0.24 和 0.35)。此外,NOS2 和 HMOX1 的表达与未成熟卵母细胞的回收呈正相关(r 分别为 0.22 和 0.40)。此外,VEGFC 水平随着受精率的增加而总体下降,与年龄无关(r 分别为-0.29)。我们发现,一批卵母细胞的受精潜能与 CC 随年龄增长对氧化应激和缺氧的反应能力有关,表明 NOS2、HMOX1 和 VEGFC 的表达可作为卵母细胞成熟和受精成功的标志物。