排卵
毛囊
黄体
细胞生物学
卵泡
卵母细胞
内科学
变硬
生物
内分泌学
发情周期
化学
男科
卵泡期
卵巢
医学
胚胎
材料科学
激素
复合材料
作者
Xiaodong Wang,Junqi Liao,Hongru Shi,Yi Zhao,Wenkai Ke,Hao Wu,Guoshi Liu,Xiang Li,Chao He
标识
DOI:10.1002/advs.202403640
摘要
Abstract Ovulation is vital for successful reproduction. Following ovulation, cumulus cells and oocyte are released, while mural granulosa cells (mGCs) remain sequestered within the post‐ovulatory follicle to form the corpus luteum. However, the mechanism underlying the confinement of mGCs has been a longstanding mystery. Here, in vitro and in vivo evidence is provided demonstrating that the stiffening of mGC‐layer serves as an evolutionarily conserved mechanism that prevents mGCs from escaping the post‐ovulatory follicles. The results from spatial transcriptome analysis and experiments reveal that focal adhesion assembly, triggered by the LH (hCG)‐cAMP‐PKA‐CREB signaling cascade, is necessary for mGC‐layer stiffening. Disrupting focal adhesion assembly through RNA interference results in stiffening failure, mGC escape, and the subsequent development of an abnormal corpus luteum characterized by decreased cell density or cavities. These findings introduce a novel concept of “mGC‐layer stiffening”, shedding light on the mechanism that prevents mGC escape from the post‐ovulatory follicle.
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