自噬
PI3K/AKT/mTOR通路
生物
西罗莫司
子宫内膜
调节器
细胞生物学
基因敲除
激活剂(遗传学)
内科学
内分泌学
癌症研究
信号转导
受体
细胞凋亡
医学
基因
遗传学
生物化学
作者
Diqi Yang,Tingting Jiang,Jianguo Liu,Beibei Zhang,Pengfei Lin,Huatao Chen,Dong Zhou,Keqiong Tang,Aihua Wang,Yaping Jin
标识
DOI:10.1093/biolre/ioy044
摘要
In domestic ruminants, a receptive endometrium is crucial for successful pregnancy. Although many essential molecular modulators and pathways have been identified during early pregnancy, the precise mechanisms regulating goat endometrial function remains largely unknown. Here, we describe a novel regulator during early pregnancy, whereby hormones increased CREB3 regulatory factor (CREBRF) expression and act as a potential activator of autophagy in endometrial epithelial cells (EECs) via the mTOR pathway. Our results showed that knockdown of CREBRF via shCREBRF hampered EECs proliferation by S-phase cell cycle arrest and significantly inhibited endometrial function. We also reported that CREBRF-mTOR-autophagy pathway plays a vital role in regulating endometrial function, with a blockade of the mTOR by rapamycin demonstrating the regulatory function on prostaglandin (PGs) secretion and cell attachment in EECs. Moreover, chloroquine pretreatment also proved the above conclusion. Collectively, our findings provide new insight into the molecular mechanisms of goat endometrial function and indicate that the CREBRF-mTOR-autophagy pathway plays a central role in PGs secretion and cell attachment.
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