Zhang Hanxue, Lanz Rainer B, Dhillon Jimmy, Soloway Paul D, Shui Bo, Ren Yi Athena
Department of Animal Science, College of Agriculture and Life Sciences, Cornell University, Ithaca, NY 14853, USA.
Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USA.
Endocrinology. 2025 May 19;166(7). doi: 10.1210/endocr/bqaf081.
The preovulatory luteinizing hormone (LH) surge orchestrates complex cellular and molecular events leading to ovulation. CCAAT/enhancer-binding proteins α and β (C/EBPα/β) are transcription factors acutely induced by the LH surge and crucial for ovulation and granulosa cell luteinization. However, biological processes (BPs) and their regulatory mechanisms downstream of C/EBPα/β in the preovulatory ovary are not completely understood. To address this knowledge gap, we generated Cebpa/bfl/fl;Pgr-Cre mutants and compared them with Cebpa/bfl/fl;Cyp19a1-Cre mutant female mice: Cebpa/bfl/fl;Cyp19a1-Cre mutants have undetectable levels of C/EBPα/β throughout the preovulatory stages and do not ovulate, aligning with previous reports; and Cebpa/bfl/fl;Pgr-Cre mutants present gradual depletion of C/EBPα/β during the late preovulatory stage and a reduced ovulation rate. Comparison of these two models indicates that sustained expression of C/EBPα/β throughout the preovulatory stages is necessary for successful ovulation and provides a unique opportunity to interrogate gene regulatory mechanisms by C/EBPα/β during different preovulatory time windows and the effect of dysregulating C/EBPα/β on ovulation-associated BPs. Our study revealed that C/EBPα/β regulate gene expression and distinct biological functions such as vascular remodeling via dose- and preovulatory stage-dependent mechanisms. These findings shed new light on the intricate mechanisms of gene regulation by C/EBPα/β downstream of the LH surge.
排卵前促黄体生成素(LH)峰协调一系列复杂的细胞和分子事件,从而导致排卵。CCAAT/增强子结合蛋白α和β(C/EBPα/β)是由LH峰急性诱导的转录因子,对排卵和颗粒细胞黄体化至关重要。然而,排卵前卵巢中C/EBPα/β下游的生物学过程(BPs)及其调控机制尚未完全明确。为了填补这一知识空白,我们构建了Cebpa/bfl/fl;Pgr-Cre突变体,并将其与Cebpa/bfl/fl;Cyp19a1-Cre突变体雌性小鼠进行比较:Cebpa/bfl/fl;Cyp19a1-Cre突变体在整个排卵前阶段都检测不到C/EBPα/β的水平,且不排卵,这与之前的报道一致;而Cebpa/bfl/fl;Pgr-Cre突变体在排卵前后期C/EBPα/β逐渐减少,排卵率降低。这两种模型的比较表明,在整个排卵前阶段持续表达C/EBPα/β对于成功排卵是必要的,并且提供了一个独特的机会来探究C/EBPα/β在不同排卵前时间窗口的基因调控机制以及C/EBPα/β失调对排卵相关生物学过程的影响。我们的研究表明,C/EBPα/β通过剂量和排卵前阶段依赖性机制调节基因表达和不同的生物学功能,如血管重塑。这些发现为LH峰下游C/EBPα/β的复杂基因调控机制提供了新的线索。