Cartwright J E, Whitley G S, Johnstone A P
Department of Cellular and Molecular Sciences, St. George's Hospital Medical School, London, United Kingdom.
Exp Cell Res. 1997 Sep 15;235(2):431-4. doi: 10.1006/excr.1997.3723.
Interactions between circulating leukocytes and vascular endothelial cells are of fundamental importance in controlling normal recirculation and migration of cells into sites of inflammation. Nitric oxide (NO), which is synthesized by vascular endothelial cells, has been reported to decrease the binding of platelets, monocytes, macrophages, and neutrophils to endothelial cells. Using NO donors and inhibitors of the enzyme NO synthase, we found no evidence that physiologically relevant levels of NO alter adhesion of purified lymphocytes to an endothelial cell line derived from human umbilical vein endothelial cells (SGHEC-7). In addition, NO donors did not alter the cell surface expression of VCAM-1, ICAM-1, or E-selectin on SGHEC-7 cells.
循环白细胞与血管内皮细胞之间的相互作用对于控制细胞正常再循环以及向炎症部位迁移至关重要。据报道,由血管内皮细胞合成的一氧化氮(NO)可减少血小板、单核细胞、巨噬细胞和中性粒细胞与内皮细胞的结合。使用NO供体和NO合酶抑制剂,我们未发现有证据表明生理相关水平的NO会改变纯化淋巴细胞与源自人脐静脉内皮细胞的内皮细胞系(SGHEC - 7)的黏附。此外,NO供体不会改变SGHEC - 7细胞上VCAM - 1、ICAM - 1或E - 选择素的细胞表面表达。