Randolph G J
Institute for Gene Therapy and Molecular Medicine, Mt. Sinai School of Medicine, 1425 Madison Avenue, Box 1496, New York, NY 10029, USA.
Semin Immunol. 2001 Oct;13(5):267-74. doi: 10.1006/smim.2001.0322.
Mobilization of dendritic cells into lymphatic vessels requires cytokine stimulation and induction of the chemokine receptor CCR7. The respective roles of the CCR7 ligands CCL19 and CCL21 in mediating migration are not fully defined, but chemotaxis to CCL19 mediates Langerhans cell exit from the epidermis. Optimal chemotaxis to CCL19 occurs when DCs are triggered with exogenous leukotriene C(4), an eicosanoid transported out of the cell via the ATP binding cassette (ABC) transporter multidrug resistance related protein 1 (MRP1, ABCC1). Indeed, MRP1 and the related multidrug resistance protein 1 (MDR1, p-glycoprotein, ABCB1) may control the intracellular and extracellular accumulation of key signaling lipids that regulate dendritic cell migration.
树突状细胞向淋巴管的动员需要细胞因子刺激和趋化因子受体CCR7的诱导。CCR7配体CCL19和CCL21在介导迁移中的各自作用尚未完全明确,但对CCL19的趋化作用介导了朗格汉斯细胞从表皮中迁出。当树突状细胞被外源性白三烯C4触发时,会出现对CCL19的最佳趋化作用,白三烯C4是一种通过ATP结合盒(ABC)转运体多药耐药相关蛋白1(MRP1,ABCC1)转运出细胞的类花生酸。实际上,MRP1和相关的多药耐药蛋白1(MDR1,P-糖蛋白,ABCB1)可能控制调节树突状细胞迁移的关键信号脂质的细胞内和细胞外积累。