From the Department of Pathology, Center for Excellence in Vascular Biology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA (R.M., G.N., F.W.L.); Department of Medicine, Center for Vascular Biology Research, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA (R.M., C.V.C.); and Department of Cell Biology, Institute of Ophthalmology, UCL, London, United Kingdom (R.M., J.G.).
Arterioscler Thromb Vasc Biol. 2013 Nov;33(11):2566-76. doi: 10.1161/ATVBAHA.113.301903. Epub 2013 Aug 29.
Although endothelial CD47, a member of the immunoglobulin superfamily, has been implicated in leukocyte diapedesis, its capacity for intracellular signaling and physical localization during this process has not been addressed in detail. This study examined endothelial CD47 spatiotemporal behavior and signaling pathways involved in regulating T-cell transendothelial migration.
By biochemical methods, transmigration assays, and live-cell microscopy techniques, we show that endothelial CD47 engagement results in intracellular calcium mobilization, increased permeability, and activation of Src and AKT1/phosphoinositide 3-kinase in brain microvascular endothelial cells. These signaling pathways converge to induce cytoskeleton remodeling and vascular endothelial cadherin phosphorylation, which are necessary steps during T-cell transendothelial migration. In addition, during T-cell migration, transmigratory cups and podo-prints enriched in CD47 appear on the surface of the endothelium, indicating that the spatial distribution of CD47 changes after its engagement. Consistent with previous findings of intercellular adhesion molecule 1, blockade of CD47 results in decreased T-cell transmigration across microvascular endothelium. The overlapping effect of intercellular adhesion molecule 1 and CD47 suggests their involvement in different steps of the diapedesis process.
These data reveal a novel role for CD47-mediated signaling in the control of the molecular network governing endothelial-dependent T-cell diapedesis.
尽管免疫球蛋白超家族的成员内皮细胞 CD47 已被牵涉到白细胞渗出过程中,但在这个过程中,其细胞内信号转导和物理定位能力尚未得到详细研究。本研究检查了内皮细胞 CD47 在调节 T 细胞穿内皮迁移过程中的时空行为和信号通路。
通过生化方法、迁移测定和活细胞显微镜技术,我们显示内皮细胞 CD47 的结合导致脑微血管内皮细胞内钙离子动员、通透性增加以及Src 和 AKT1/磷酸肌醇 3-激酶的激活。这些信号通路汇聚诱导细胞骨架重塑和血管内皮钙黏蛋白磷酸化,这是 T 细胞穿内皮迁移过程中的必要步骤。此外,在 T 细胞迁移过程中,富含 CD47 的迁移杯和足印出现在内皮表面,表明 CD47 的空间分布在其结合后发生变化。与细胞间黏附分子 1 的先前发现一致,CD47 阻断导致 T 细胞穿过微血管内皮的迁移减少。细胞间黏附分子 1 和 CD47 的重叠效应表明它们参与了渗出过程的不同步骤。
这些数据揭示了 CD47 介导的信号在控制内皮依赖性 T 细胞渗出的分子网络中的新作用。