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氧诱导视网膜病变模型中 EphrinB2 和 EphB4 的血管表达改变。

Altered vascular expression of EphrinB2 and EphB4 in a model of oxygen-induced retinopathy.

机构信息

Department of Pediatrics, Oregon Health & Science University, Portland, Oregon, USA.

出版信息

Dev Dyn. 2010 Jun;239(6):1695-707. doi: 10.1002/dvdy.22306.

Abstract

EphrinB2 ligands and EphB4 receptors are expressed on endothelial cells (EC) of arteries and veins, respectively, and are essential for vascular development. To understand how these molecules regulate retinal neovascularization (NV), we evaluated their expression in a model of oxygen-induced retinopathy (OIR). EphrinB2 and EphB4 were expressed on arterial and venous trunks, respectively, and on a subset of deep capillary vessels. EphB4 expression was reduced following hyperoxia, while ephrinB2 expression remained unaltered. In addition, a subset of EphB4-positive veins regressed in a caspase-3-dependent manner during hyperoxia. Arteriovenous malformations were also observed with loss of arterial-venous boundaries. Finally, both ephrinB2 and EphB4 were expressed on a subset of neovascular tufts following hyperoxia. These data confirm the contribution of ECs from both venous and arterial origins to the development of retinal NV.

摘要

EphrinB2 配体和 EphB4 受体分别在动脉和静脉内皮细胞 (EC) 上表达,对于血管发育至关重要。为了了解这些分子如何调节视网膜新生血管化 (NV),我们在氧诱导的视网膜病变 (OIR) 模型中评估了它们的表达。EphrinB2 和 EphB4 分别在动脉和静脉干以及一部分深毛细血管上表达。EphB4 表达在高氧条件下减少,而 EphrinB2 表达保持不变。此外,在高氧条件下,一部分 EphB4 阳性静脉以半胱天冬酶-3 依赖的方式退化。还观察到动静脉畸形伴有动脉静脉边界丧失。最后,在高氧条件下,一部分新生血管丛上也表达 EphrinB2 和 EphB4。这些数据证实了来自静脉和动脉起源的 EC 对视网膜 NV 发展的贡献。

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