基础医学与临床 ›› 2008, Vol. 28 ›› Issue (7): 702-706.

• 研究论文 • 上一篇    下一篇

CCR5介导6T-CEM 细胞穿过人脑微血管内皮细胞单层能力分析

马怡然 尚德淑 赵伟东 方文刚 陈誉华   

  1. 中国医科大学基础医学院发育生物学教研室 中国医科大学基础医学院发育生物学教研室 中国医科大学基础医学院发育生物学教研室 中国医科大学基础医学院发育生物学教研室 中国医科大学基础医学院发育生物学教研室
  • 收稿日期:2007-06-14 修回日期:2007-09-21 出版日期:2008-07-25 发布日期:2008-07-25
  • 通讯作者: 马怡然

CCR5 promotes the migration of 6T-CEM through Human Brain Microvascular Endothelial Cells Monolayer

Yi-ran MA, De-shu SHANG, Wei-dong ZHAO, Wen-gang FANG, Yu-hua CHEN   

  • Received:2007-06-14 Revised:2007-09-21 Online:2008-07-25 Published:2008-07-25
  • Contact: Yi-ran MA,

摘要: 摘要:目的 我们的研究已表明AD病人T淋巴细胞穿过人脑微血管内皮细胞(HBMEC)单层能力高于同年龄正常人与其过表达MIP-1α密切相关,为了分析AD病人T淋巴细胞穿过HBMEC单层机制,选用高表达MIP-1α的人淋巴细胞系6T-CEM作为模式细胞对6T-CEM穿过人脑微血管内皮细胞单层进行探讨。 方法 通过应用免疫荧光和蛋白免疫印迹技术,真核表达载体的构建与细胞转染技术,以及跨内皮迁移和抗体封闭实验的进行,集中探讨了HBMEC 膜受体CCR5在6T-CEM细胞穿过HBMEC单层过程中作用。结果 在6T-CEM 细胞与HBMEC 单层单独孵育过程中,引起HBMEC 膜受体CCR5 表达变化;HBMEC膜受体CCR5的高表达使6T-CEM细胞穿过HBMEC单层能力增强。结论 HBMEC膜受体CCR5参与了6T-CEM细胞穿过HBMEC单层过程。

关键词: 趋化因子受体5, 人T淋巴细胞白血病细胞系, 人脑微血管内皮细胞

Abstract: Abstract: Objective: We have showed the stronger ability to migrate through human brain microvascular endothelial cells (HBMECs) in peripheral T lymphocytes of AD patients than age-matched is associated with a significantly higher macrophage inflammatory protein-1α (MIP-1α) expression of T lymphocyte. In order to explore the mechanism of the transendothelial migration of T lymphocytes further, we choose 6T-CEM cells expressing MIP-1α as a model cell line of AD patients’ T lymphocytes to investigate this mechanism. Methods :Immunofluorescence, western blot, plasmid construction and transfection, transendothelial migration and endothelial permeability assay are used to explore the progress of the transendothelial migration of T cells. Results: The expressions of CCR5 on HBMECs which incubated with 6T-CEM cells were detected. The induced expressions of CCR5 can enhance the migration of 6T-CEM cells through HBMEC monolayer. Conclusion: CCR5 on HBMECs might be involved in the transendothelial migration of T lymphocytes .

Key words: CCR5, 6T-CEM cells, HBMEC