Oxygen modifies artery differentiation and network morphogenesis in the retinal vasculature

被引:29
作者
Claxton, S
Fruttiger, M
机构
[1] UCL, Inst Ophthalmol, London WC1E 6BT, England
[2] UCL, Wolfson Inst Biomed Res, London WC1E 6BT, England
[3] UCL, Dept Biol, London WC1E 6BT, England
基金
英国惠康基金;
关键词
artery vein differentiation; hypoxia; D114; ephrin B4; msr/apj; alpha SMA; mice; retinal vasculature; endothelial cells; smooth muscle cells;
D O I
10.1002/dvdy.20407
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
The mechanisms that control differentiation of immature blood vessels into either arteries or veins are not well understood. Because oxygen tension in arteries is higher than in veins, oxygen has the potential to be an instructive signal for artery/vein (AV) differentiation. We test this hypothesis by exposing newborn mice to moderate hypoxia (10% atmospheric oxygen) and studying AV differentiation in the developing retinal vasculature. Forming retinal arteries fail to express the artery-specific markers Delta-like 4 (Dll4) and EphrinB2 during hypoxia. However, other aspects of AV differentiation are retained such as high levels of alpha smooth muscle actin in arterial mural cells and vein-specific expression of the msr/apj gene. The capillary network between arteries and veins is denser, and capillaries expressing the venous marker msr/apj are found in territories normally occupied by arterial capillaries. Thus, it appears that high oxygen in arterial blood is required for arterial expression of Dll4 and EphrinB2, which could be involved in cell-cell repulsion pathways that dictate the normal segregation of arteries and veins. (c) 2005 Wiley-Liss, Inc.
引用
收藏
页码:822 / 828
页数:7
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