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血管发生与血管生成。

Vasculogenesis and angiogenesis.

作者信息

Patan Sybill

机构信息

Division of Cardiology, Albert Einstein College of Medicine, Yeshiva University, Bronx, New York 10461, USA.

出版信息

Cancer Treat Res. 2004;117:3-32. doi: 10.1007/978-1-4419-8871-3_1.

Abstract

Two distinct mechanisms, vasculogenesis and angiogenesis implement the formation of the vascular network in the embryo. Vasculogenesis gives rise to the heart and the first primitive vascular plexus inside the embryo and in its surrounding membranes, as the yolk sac circulation. Angiogenesis is responsible for the remodeling and expansion of this network. While vasculogenesis refers to in situ differentiation and growth of blood vessels from mesodermal derived hemangioblasts, angiogenesis comprises two different mechanisms: endothelial sprouting and intussusceptive microvascular growth (IMG). The sprouting process is based on endothelial cell migration, proliferation and tube formation. IMG divides existing vessel lumens by formation and insertion of tissue folds and columns of interstitial tissue into the vessel lumen. The latter are termed interstitial or intervascular tissue structures (ITSs) and tissue pillars or posts. Intussusception also includes the establishment of new vessels by in situ loop formation in the wall of large veins. The molecular regulation of these distinct mechanisms is discussed in respect to the most important positive regulators, VEGF and its receptors flk-1 (KDR) and flt-1, the Angiopoietin/tie system and the ephrin-B/EpH-B system. The cellular mechanisms and the molecular regulation of angiogenesis in the pathological state are summarized and the differences of physiological and pathological angiogenesis elaborated.

摘要

两种不同的机制,即血管发生和血管生成,实现了胚胎中血管网络的形成。血管发生产生了心脏以及胚胎内部及其周围膜中的第一个原始血管丛,如卵黄囊循环。血管生成则负责该网络的重塑和扩展。血管发生是指从中胚层来源的成血管细胞原位分化并生长出血管,而血管生成包括两种不同的机制:内皮细胞芽生和套入性微血管生长(IMG)。芽生过程基于内皮细胞的迁移、增殖和管腔形成。IMG通过形成组织褶皱并将间质组织柱插入血管腔来分隔现有的血管腔。后者被称为间质或血管间组织结构(ITSs)以及组织柱或支柱。套入还包括通过在大静脉壁上原位形成环来建立新血管。本文将针对最重要的正向调节因子,即血管内皮生长因子(VEGF)及其受体flk-1(KDR)和flt-1、血管生成素/tie系统以及ephrin-B/EpH-B系统,讨论这些不同机制的分子调控。总结了病理状态下血管生成的细胞机制和分子调控,并阐述了生理性和病理性血管生成的差异。

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