Targeted hypoxia-inducible factor 1-alpha (HIF1A) stabilization during in vitro maturation of bovine cumulus-oocyte complexes increases blastocyst rates

在体外成熟牛卵丘-卵母细胞复合体的过程中,靶向稳定缺氧诱导因子1α (HIF1A) 可提高囊胚形成率

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Abstract

In vitro production (IVP) of bovine embryos frequently results in varying blastocyst yields, partly because culture conditions fail to support optimal oocyte and embryo development. In vivo, cumulus-oocyte complexes (COCs) mature under hypoxic conditions, and while in vitro protocols try to mimic the natural conditions, standard in vitro maturation (IVM) is typically performed under normoxia, guided largely by empirical outcomes rather than a biological understanding. We hypothesized that IVP efficiency would be improved by stabilization of hypoxia-inducible factor 1-alpha (HIF1A), via pharmacological inhibition of prolyl hydroxylase domain (PHD) activity, during IVM. To test this, we treated COCs with varying concentrations of Roxadustat, a PHD inhibitor. Low-dose treatment (25 µM) stabilized and significantly enhanced blastocyst formation (p < 0.01), while higher doses (100 µM) impaired maturation rates (p < 0.05). Interestingly, HIF1A mRNA expression decreased in treated groups, whereas protein levels remained stable, suggesting a feedback mechanism that may prevent excessive and potentially detrimental HIF1A activity. Additionally, we assessed the expression of markers related to cumulus expansion (HAS2, TNFAIP6), meiotic resumption (TMSB4), and cell proliferation (PCNA). However, their expression did not correlate with the increased blastocyst formation after Roxadustat treatment. Furthermore, PHD inhibition during in vitro culture (IVC) had no effect on cleavage rates (p > 0.05), but higher doses led to reduced blastocyst development (p < 0.01). These findings suggest that the benefits of HIF1A stabilization are specific to the maturation phase, likely by supporting cumulus-oocyte interactions critical for establishing developmental competence, rather than by directly influencing fertilization or early cleavage. These findings highlight the potential of fine-tuned HIF1A modulation to improve IVP efficiency. Further studies should elucidate the downstream molecular mechanisms and assess post-transfer development outcomes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1038/s41598-025-33894-8.

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