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FoxO1 在 VEGF 表达中的转录活性及其以外的作用:功能性血管生成中的关键调节因子?

FoxO1 transcriptional activities in VEGF expression and beyond: a key regulator in functional angiogenesis?

机构信息

Division of Hematology and Oncology, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.

Laboratory of Vascular Pathobiology, Blood Research Institute, Blood Center of Wisconsin, Milwaukee, Wisconsin, USA.

出版信息

J Pathol. 2018 Jul;245(3):255-257. doi: 10.1002/path.5088. Epub 2018 May 23.

Abstract

FoxO1 has emerged as an important regulator of angiogenesis. Recent work published in this Journal shows that FoxO1 regulates VEGF expression in keratinocytes and is required for angiogenesis in wound healing. Since FoxO1 also regulates CD36 transcription, and endothelial cell differentiation and vascular maturation, this transcription factor may be essential for the formation of functional vascular networks via coupling the regulation of CD36 in vascular endothelial cells under physiological and pathological conditions. Although many outstanding questions remain to be answered, the mechanisms by which FoxO1 regulates VEGF in keratinocytes provide insight into the development of functional angiogenesis and further our understanding of vascular biology. Copyright © 2018 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.

摘要

FoxO1 已成为血管生成的重要调节因子。本刊最近发表的一项研究表明,FoxO1 可调节角质细胞中 VEGF 的表达,是创伤愈合中血管生成所必需的。由于 FoxO1 还可调节 CD36 的转录,以及内皮细胞的分化和血管的成熟,因此该转录因子可能通过在生理和病理条件下调节血管内皮细胞中 CD36 的转录,对于形成功能性血管网络至关重要。尽管仍有许多悬而未决的问题,但 FoxO1 调节角质细胞中 VEGF 的机制为功能性血管生成的发展提供了深入的了解,并进一步加深了我们对血管生物学的认识。版权所有 © 2018 英国和爱尔兰病理学会。由 John Wiley & Sons, Ltd. 出版。

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