血管生成
福克斯O1
伤口愈合
血管内皮生长因子A
肉芽组织
癌症研究
新生血管
转录因子
生物
免疫学
血管内皮生长因子
血管内皮生长因子受体
遗传学
基因
作者
Hyeran Helen Jeon,Quan Yu,Yongjian Lu,Evelyn Spencer,Chanyi Lu,Tatyana N. Milovanova,Yang Yang,Chenying Zhang,Olga Stepanchenko,Rameen P. Vafa,Paulo G. Coelho,Dana T. Graves
摘要
Angiogenesis is a critical aspect of wound healing. We investigated the role of keratinocytes in promoting angiogenesis in mice with lineage-specific deletion of the transcription factor FOXO1. The results indicate that keratinocyte-specific deletion of Foxo1 reduces VEGFA expression in mucosal and skin wounds and leads to reduced endothelial cell proliferation, reduced angiogenesis, and impaired re-epithelialization and granulation tissue formation. In vitro FOXO1 was needed for VEGFA transcription and expression. In a porcine dermal wound-healing model that closely resembles healing in humans, local application of a FOXO1 inhibitor reduced angiogenesis. This is the first report that FOXO1 directly regulates VEGFA expression and that FOXO1 is needed for normal angiogenesis during wound healing. Copyright © 2018 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
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