Department of Pharmacology and Ischemic/Hypoxic Disease Institute, College of Medicine, Seoul National University, 103 Daehangno, Jongno-Gu, Seoul 110-799, Republic of Korea.
Cell Immunol. 2011;267(1):23-9. doi: 10.1016/j.cellimm.2010.10.011. Epub 2010 Nov 3.
BST2 is a type II transmembrane protein that had been initially identified as a surface molecule expressed on terminally differentiated B cells. Here, we characterize the expression of BST2 in human endothelial cells, HUVECs. IFN-γ, among various inflammatory stimuli, dramatically upregulates BST2 expression in HUVECs. We also address a novel putative role of BST2 in IFN-γ-stimulated HUVECs as an intercellular adhesion-related molecule. We show that purified extracellular domain of BST2 protein specifically and significantly decreased the adhesion of human monocytes to HUVECs, which suggests that IFN-γ-induced BST2 expression may be involved in monocyte migration from blood through the endothelium to the inflammation site. Furthermore, we show that the monocytic cell line U937 can directly adhere to BST2 extracellular domain-coated tissue culture wells. These results provide experimental evidence to support a novel role for BST2 in the interaction between human monocyte and IFN-γ-stimulated endothelium.
BST2 是一种 II 型跨膜蛋白,最初被鉴定为终末分化 B 细胞表面表达的分子。在这里,我们描述了 BST2 在人血管内皮细胞(HUVECs)中的表达。IFN-γ 等各种炎症刺激物可显著上调 HUVECs 中 BST2 的表达。我们还提出了 BST2 在 IFN-γ 刺激的 HUVECs 中的一个新的假定作用,作为一种细胞间黏附相关分子。我们发现 BST2 蛋白的纯化细胞外结构域可特异性和显著降低人单核细胞与 HUVECs 的黏附,这表明 IFN-γ 诱导的 BST2 表达可能参与了单核细胞从血液穿过内皮迁移到炎症部位的过程。此外,我们发现单核细胞系 U937 可直接黏附于包被有 BST2 细胞外结构域的组织培养孔。这些结果为 BST2 在人单核细胞与 IFN-γ 刺激的内皮细胞相互作用中的新作用提供了实验证据。