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本文引用的文献

1
Role of Notch in endothelial biology.Notch 在血管内皮生物学中的作用。
Angiogenesis. 2021 May;24(2):237-250. doi: 10.1007/s10456-021-09793-7. Epub 2021 May 29.
2
Control of endothelial quiescence by FOXO-regulated metabolites.FOXO 调控代谢物控制血管内皮细胞静止
Nat Cell Biol. 2021 Apr;23(4):413-423. doi: 10.1038/s41556-021-00637-6. Epub 2021 Apr 1.
3
The quiescent endothelium: signalling pathways regulating organ-specific endothelial normalcy.静止内皮:调节器官特异性内皮正常状态的信号通路
Nat Rev Cardiol. 2021 Aug;18(8):565-580. doi: 10.1038/s41569-021-00517-4. Epub 2021 Feb 24.
4
Aberrant Activation of Notch1 Signaling in Glomerular Endothelium Induces Albuminuria.肾小球内皮细胞中 Notch1 信号的异常激活导致白蛋白尿。
Circ Res. 2021 Mar 5;128(5):602-618. doi: 10.1161/CIRCRESAHA.120.316970. Epub 2021 Jan 13.
5
Network-based screen in iPSC-derived cells reveals therapeutic candidate for heart valve disease.基于网络的 iPSC 衍生细胞筛选揭示了心脏瓣膜疾病的治疗候选药物。
Science. 2021 Feb 12;371(6530). doi: 10.1126/science.abd0724. Epub 2020 Dec 10.
6
Arterialization requires the timely suppression of cell growth.动脉化需要及时抑制细胞生长。
Nature. 2021 Jan;589(7842):437-441. doi: 10.1038/s41586-020-3018-x. Epub 2020 Dec 9.
7
Jagged1-Notch1-deployed tumor perivascular niche promotes breast cancer stem cell phenotype through Zeb1.锯齿状 1-Notch1 靶向的肿瘤血管周龛促进乳腺癌干细胞表型通过 Zeb1。
Nat Commun. 2020 Oct 12;11(1):5129. doi: 10.1038/s41467-020-18860-4.
8
RHOQ is induced by DLL4 and regulates angiogenesis by determining the intracellular route of the Notch intracellular domain.RHOQ 由 DLL4 诱导,并通过确定 Notch 细胞内结构域的细胞内途径来调节血管生成。
Angiogenesis. 2020 Aug;23(3):493-513. doi: 10.1007/s10456-020-09726-w. Epub 2020 Jun 6.
9
Shear stress activates ADAM10 sheddase to regulate Notch1 via the Piezo1 force sensor in endothelial cells.切应力通过内皮细胞中的 Piezo1 力传感器激活 ADAM10 剪切酶来调节 Notch1。
Elife. 2020 Jun 2;9:e50684. doi: 10.7554/eLife.50684.
10
Endothelial Notch signaling controls insulin transport in muscle.内皮细胞Notch信号通路调控肌肉中的胰岛素转运。
EMBO Mol Med. 2020 Apr 7;12(4):e09271. doi: 10.15252/emmm.201809271. Epub 2020 Mar 18.

血管中的Notch信号:血管生成与血管分泌功能

Notch Signaling in the Vasculature: Angiogenesis and Angiocrine Functions.

作者信息

Hasan Sana S, Fischer Andreas

机构信息

Division Vascular Signaling and Cancer, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany.

Institute for Clinical Chemistry, University Medical Center Göttingen, 37075 Göttingen, Germany.

出版信息

Cold Spring Harb Perspect Med. 2023 Feb 1;13(2):a041166. doi: 10.1101/cshperspect.a041166.

DOI:10.1101/cshperspect.a041166
PMID:35667708
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9899647/
Abstract

Formation of a functional blood vessel network is a complex process tightly controlled by pro- and antiangiogenic signals released within the local microenvironment or delivered through the bloodstream. Endothelial cells precisely integrate such temporal and spatial changes in extracellular signals and generate an orchestrated response by modulating signaling transduction, gene expression, and metabolism. A key regulator in vessel formation is Notch signaling, which controls endothelial cell specification, proliferation, migration, adhesion, and arteriovenous differentiation. This review summarizes the molecular biology of endothelial Notch signaling and how it controls angiogenesis and maintenance of the established, quiescent vasculature. In addition, recent progress in the understanding of Notch signaling in endothelial cells for controlling organ homeostasis by transcriptional regulation of angiocrine factors and its relevance to disease will be discussed.

摘要

功能性血管网络的形成是一个复杂的过程,受到局部微环境中释放的促血管生成和抗血管生成信号或通过血流传递的信号的严格控制。内皮细胞精确整合细胞外信号的这种时空变化,并通过调节信号转导、基因表达和代谢产生协调反应。血管形成中的一个关键调节因子是Notch信号,它控制内皮细胞的特化、增殖、迁移、黏附以及动静脉分化。本综述总结了内皮Notch信号的分子生物学及其如何控制血管生成和维持已建立的静止脉管系统。此外,还将讨论在理解内皮细胞中Notch信号通过血管分泌因子的转录调控来控制器官稳态及其与疾病的相关性方面的最新进展。