Papadopoulos E J, Sassetti C, Saeki H, Yamada N, Kawamura T, Fitzhugh D J, Saraf M A, Schall T, Blauvelt A, Rosen S D, Hwang S T
Dermatology Branch, National Cancer Institute, Bethesda, USA.
Eur J Immunol. 1999 Aug;29(8):2551-9. doi: 10.1002/(SICI)1521-4141(199908)29:08<2551::AID-IMMU2551>3.0.CO;2-T.
The lone CX3C chemokine, fractalkine (FK), is expressed in a membrane-bound form on activated endothelial cells and mediates attachment and firm adhesion of T cells, monocytes and NK cells. We now show that FK is associated with dendritic cells (DC) in epidermis and lymphoid organs. In normal human skin, dual-color fluorescence microscopy co-localized FK expression with Langerhans cells expressing CD1a. In tonsil, FK-positive DC expressed CD83, a marker for mature DC. Human and murine cultured DC up-regulated FK mRNA expression with maturation. Furthermore, CD40 ligation, but not TNF-alpha or lipopolysaccharide treatment, of activated, migratory DC that had migrated from skin explants resulted in a 2.5-fold increase of surface expression of FK without significant alterations of expression of CD80, CD86, CD54 or MHC class II. Since FK mediates adhesion of T cells to activated endothelial cells, the increased expression of FK during DC maturation (and particularly by CD40 ligation) may play a role in the ability of T cells and mature DC to form conjugates and engage in cell-cell communication.
唯一的CX3C趋化因子,fractalkine(FK),在活化的内皮细胞上以膜结合形式表达,并介导T细胞、单核细胞和自然杀伤细胞的黏附和牢固黏附。我们现在发现FK与表皮和淋巴器官中的树突状细胞(DC)相关。在正常人类皮肤中,双色荧光显微镜显示FK表达与表达CD1a的朗格汉斯细胞共定位。在扁桃体中,FK阳性DC表达CD83,这是成熟DC的标志物。人和小鼠培养的DC随着成熟而上调FK mRNA表达。此外,对从皮肤外植体迁移而来的活化迁移DC进行CD40连接,但不进行TNF-α或脂多糖处理,导致FK表面表达增加2.5倍,而CD80、CD86、CD54或MHC II类分子的表达无显著变化。由于FK介导T细胞与活化内皮细胞的黏附,DC成熟过程中(特别是通过CD40连接)FK表达的增加可能在T细胞与成熟DC形成共轭物并进行细胞间通讯的能力中发挥作用。