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中枢神经系统的发育性血管生成

Developmental angiogenesis of the central nervous system.

作者信息

Mancuso Michael R, Kuhnert Frank, Kuo Calvin J

机构信息

Stanford University School of Medicine. Division of Hematology, Stanford, CA.

出版信息

Lymphat Res Biol. 2008;6(3-4):173-80. doi: 10.1089/lrb.2008.1014.

DOI:10.1089/lrb.2008.1014
PMID:19093790
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2712664/
Abstract

The vasculature of the central nervous system (CNS) is highly specialized with a blood-brain-barrier, reciprocal neuroepithelial-endothelial cell interactions and extensive pericyte coverage. Developmentally, numerous important signaling pathways participate in CNS angiogenesis to orchestrate the precise timing and spatial arrangement of the complex CNS vascular network. From a therapeutic standpoint, the CNS vasculature has attracted increased attention since many human ailments, such as stroke, retinopathy, cancer and autoimmune disease are intimately associated with the biology of CNS blood vessels. This review focuses on growth factor pathways that have been shown to be important in developmental CNS vascularization through studies of mouse genetic models and human diseases.

摘要

中枢神经系统(CNS)的脉管系统高度特化,具有血脑屏障、神经上皮细胞与内皮细胞的相互作用以及广泛的周细胞覆盖。在发育过程中,众多重要的信号通路参与中枢神经系统血管生成,以协调复杂的中枢神经系统血管网络的精确时间和空间排列。从治疗角度来看,中枢神经系统脉管系统已引起越来越多的关注,因为许多人类疾病,如中风、视网膜病变、癌症和自身免疫性疾病都与中枢神经系统血管生物学密切相关。本综述重点关注通过小鼠遗传模型和人类疾病研究已证明在中枢神经系统发育性血管生成中起重要作用的生长因子通路。

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本文引用的文献

1
Canonical Wnt signaling regulates organ-specific assembly and differentiation of CNS vasculature.经典Wnt信号通路调控中枢神经系统血管的器官特异性组装和分化。
Science. 2008 Nov 21;322(5905):1247-50. doi: 10.1126/science.1164594.
2
Wnt/beta-catenin signaling controls development of the blood-brain barrier.Wnt/β-连环蛋白信号通路控制血脑屏障的发育。
J Cell Biol. 2008 Nov 3;183(3):409-17. doi: 10.1083/jcb.200806024. Epub 2008 Oct 27.
3
Crosstalk between vascular endothelial growth factor, notch, and transforming growth factor-beta in vascular morphogenesis.血管内皮生长因子、Notch信号通路与转化生长因子-β在血管形态发生中的相互作用
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4
Robo4 stabilizes the vascular network by inhibiting pathologic angiogenesis and endothelial hyperpermeability.Robo4通过抑制病理性血管生成和内皮细胞高通透性来稳定血管网络。
Nat Med. 2008 Apr;14(4):448-53. doi: 10.1038/nm1742. Epub 2008 Mar 16.
5
Blockade of Dll4 inhibits tumour growth by promoting non-productive angiogenesis.抑制Dll4可通过促进无效血管生成来抑制肿瘤生长。
Novartis Found Symp. 2007;283:106-20; discussion 121-5, 238-41.
6
Targeting microRNA expression to regulate angiogenesis.靶向微小RNA表达以调控血管生成。
Trends Pharmacol Sci. 2008 Jan;29(1):12-5. doi: 10.1016/j.tips.2007.10.014. Epub 2007 Dec 18.
7
Regulation of angiogenesis through a microRNA (miR-130a) that down-regulates antiangiogenic homeobox genes GAX and HOXA5.通过下调抗血管生成同源盒基因GAX和HOXA5的微小RNA(miR-130a)对血管生成进行调控。
Blood. 2008 Feb 1;111(3):1217-26. doi: 10.1182/blood-2007-07-104133. Epub 2007 Oct 23.
8
Slit-Robo interactions during cortical development.皮层发育过程中的Slit-Robo相互作用。
J Anat. 2007 Aug;211(2):188-98. doi: 10.1111/j.1469-7580.2007.00750.x. Epub 2007 Jun 6.
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Structural basis for autoinhibition of Notch.Notch自抑制的结构基础。
Nat Struct Mol Biol. 2007 Apr;14(4):295-300. doi: 10.1038/nsmb1227. Epub 2007 Apr 1.
10
Notch signaling is necessary for epithelial growth arrest by TGF-beta.Notch信号传导对于转化生长因子β(TGF-β)介导的上皮生长停滞是必需的。
J Cell Biol. 2007 Feb 26;176(5):695-707. doi: 10.1083/jcb.200612129.