CD47型
整合素
细胞生物学
内皮
跨膜蛋白
Jurkat细胞
血栓反应蛋白1
受体
生物
免疫学
癌症研究
免疫系统
T细胞
内分泌学
生物化学
血管生成
吞噬作用
作者
Michel Ticchioni,Vincent Raimondi,Laurence Lamy,John Wijdenes,Frederik P. Lindberg,Eric J. Brown,Alain Bernard
标识
DOI:10.1096/fj.99-0833com
摘要
ABSTRACT Integrin‐associated protein (CD47/IAP) is a pentaspan molecule that regulates integrin functions. We prepared a CD47‐deficient Jurkat T cell line to assess its role in the arrest of T cells on inflammatory endothelium. Under flow conditions, constitutive arrest of CD47‐deficient cells is strongly decreased as compared to the original cell line, whereas reexpression of CD47 reestablishes their ability to stop. Moreover, cells transfected with a chimera made with the extracellular portion of CD47 and the transmembrane domain of CD7 or several truncated forms of CD47 show that the first transmembrane domain and a short cytoplasmic loop are sufficient for this process. CD47 effect is indirect and depends mainly on the α 4β1/VCAM‐1 pathway, as shown by blocking antibodies. We detected on endothelium the two CD47 counter receptors known to date: thrombospondin and SIRP1 α . Blocking experiments show that both are involved. Overall, CD47 participates in the constitutive arrest of T lymphocytes on inflamed vascular endothelium by up‐regulating a 4β1 integrins.—Ticchioni, M., Raimondi, V., Lamy, L., Wijdenes, J., Lindberg, F. P., Brown, E. J., Bernard, A. Integrin‐associated protein (CD47/IAP) contributes to T cell arrest on inflammatory vascular endothelium under flow. FASEB J. 15, 341‐350 (2001)
科研通智能强力驱动
Strongly Powered by AbleSci AI