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细胞外基质的破坏通过β-连环蛋白信号逐渐损害中枢神经系统血管的成熟。

Disruption of the Extracellular Matrix Progressively Impairs Central Nervous System Vascular Maturation Downstream of β-Catenin Signaling.

机构信息

From the Department of Medical and Health Sciences, Linköpings Universitet, Linköping, Sweden (L.D.J.).

Department of Physiology and Pharmacology (B.H., V.M.L., J.K.), Karolinska Institutet, Stockholm, Sweden.

出版信息

Arterioscler Thromb Vasc Biol. 2019 Jul;39(7):1432-1447. doi: 10.1161/ATVBAHA.119.312388. Epub 2019 May 9.

Abstract

Objective- The Wnt/β-catenin pathway orchestrates development of the blood-brain barrier, but the downstream mechanisms involved at different developmental windows and in different central nervous system (CNS) tissues have remained elusive. Approach and Results- Here, we create a new mouse model allowing spatiotemporal investigations of Wnt/β-catenin signaling by induced overexpression of Axin1, an inhibitor of β-catenin signaling, specifically in endothelial cells ( Axin1 - ). AOE (Axin1 overexpression) in Axin1 - mice at stages following the initial vascular invasion of the CNS did not impair angiogenesis but led to premature vascular regression followed by progressive dilation and inhibition of vascular maturation resulting in forebrain-specific hemorrhage 4 days post-AOE. Analysis of the temporal Wnt/β-catenin driven CNS vascular development in zebrafish also suggested that Axin1 - led to CNS vascular regression and impaired maturation but not inhibition of ongoing angiogenesis within the CNS. Transcriptomic profiling of isolated, β-catenin signaling-deficient endothelial cells during early blood-brain barrier-development (E11.5) revealed ECM (extracellular matrix) proteins as one of the most severely deregulated clusters. Among the 20 genes constituting the forebrain endothelial cell-specific response signature, 8 ( Adamtsl2, Apod, Ctsw, Htra3, Pglyrp1, Spock2, Ttyh2, and Wfdc1) encoded bona fide ECM proteins. This specific β-catenin-responsive ECM signature was also repressed in Axin1 - and endothelial cell-specific β-catenin-knockout mice ( Ctnnb1-KO) during initial blood-brain barrier maturation (E14.5), consistent with an important role of Wnt/β-catenin signaling in orchestrating the development of the forebrain vascular ECM. Conclusions- These results suggest a novel mechanism of establishing a CNS endothelium-specific ECM signature downstream of Wnt-β-catenin that impact spatiotemporally on blood-brain barrier differentiation during forebrain vessel development. Visual Overview- An online visual overview is available for this article.

摘要

目的

Wnt/β-catenin 通路协调血脑屏障的发育,但在不同的发育窗口和不同的中枢神经系统 (CNS) 组织中涉及的下游机制仍不清楚。

方法和结果

在这里,我们创建了一种新的小鼠模型,通过诱导过表达 Axin1(β-catenin 信号的抑制剂),允许在时空上研究 Wnt/β-catenin 信号,Axin1 特异性在血管内皮细胞 (Axin1 - ) 中过表达。在 CNS 初始血管侵袭后阶段,在 Axin1 - 小鼠中进行 Axin1 过表达 (AOE) 不会损害血管生成,但会导致早期血管退化,随后进行血管成熟的进行性扩张和抑制,导致 AOE 后 4 天出现前脑特异性出血。对斑马鱼中时空 Wnt/β-catenin 驱动的 CNS 血管发育的分析也表明,Axin1 - 导致 CNS 血管退化和成熟受损,但不会抑制 CNS 内正在进行的血管生成。在早期血脑屏障发育 (E11.5) 期间对分离的、β-catenin 信号缺失的内皮细胞进行转录组谱分析显示细胞外基质 (ECM) 蛋白是最严重失调的簇之一。在构成前脑内皮细胞特异性反应特征的 20 个基因中,有 8 个(Adamtsl2、Apod、Ctsw、Htra3、Pglyrp1、Spock2、Ttyh2 和 Wfdc1)编码真正的 ECM 蛋白。在初始血脑屏障成熟 (E14.5) 期间,Axin1 - 和内皮细胞特异性 β-catenin 敲除小鼠 (Ctnnb1-KO) 中也抑制了这种特定的 β-catenin 反应性 ECM 特征,这表明 Wnt/β-catenin 信号在协调前脑血管 ECM 的发育中起着重要作用。

结论

这些结果表明了一种在 Wnt-β-catenin 下游建立 CNS 内皮细胞特异性 ECM 特征的新机制,该机制在影响前脑血管发育过程中血脑屏障分化的时空上具有重要作用。

可视化概述

本文提供了一个在线可视化概述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25e0/6636811/ff8013b5700a/atv-39-1432-g001.jpg

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