血管生成
KLF4公司
化学
内科学
医学
生物化学
基因
诱导多能干细胞
胚胎干细胞
作者
Can Cao,Yuling Zhou,Yu Zhang,Yucong Ma,Shujin Du,Lijie Fan,Ruobing Niu,Yingmei Zhang,Ming He
出处
期刊:iScience
[Elsevier]
日期:2022-06-02
卷期号:25 (7): 104509-104509
被引量:11
标识
DOI:10.1016/j.isci.2022.104509
摘要
Endometrial angiogenesis is necessary for good endometrial receptivity. Krüppel-like factor 4 (KLF4) is a transcription factor that is essential for regulating angiogenesis. Here we found that vascular endothelial growth factor A (VEGFA) can form a positive feedback loop with KLF4 to promote the proliferation and migration of human endometrial microvascular endothelial cells (HEMECs) and inhibit cell apoptosis. General control non-derepressible 5 (GCN5) is also time-dependent on VEGFA and participates in the KLF4-VEGFA loop. In addition, we found that GCN5 is a succinyltransferase that modulates the succinylation of histones and nonhistones. GCN5 interacts with KLF4 and is recruited to the KLF4-binding site of the VEGFA promoter to succinylate H3K79, which initiates gene transcription epigenetically. For nonhistones, GCN5 succinylates KLF4 that is activated by ERK signaling in HEMECs treated with VEGFA to increase its transcription activity. These results demonstrate KLF4-VEGFA positive feedback loop is regulated by epigenetics, which contributes to endometrial angiogenesis.
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