Opposite fate of endocytosed CCR7 and its ligands: Recycling versus degradation

被引:106
作者
Otero, Carolina
Groettrup, Marcus
Legler, Daniel F.
机构
[1] Univ Konstanz, Biotechnol Inst Thurgau, CH-8274 Tagerwilen, Switzerland
[2] Univ Konstanz, Div Immunol, Dept Biol, Constance, Germany
关键词
HIGH ENDOTHELIAL VENULES; CHEMOKINE RECEPTOR CCR7; AGONIST-INDUCED ENDOCYTOSIS; DENDRITIC CELL MATURATION; SECONDARY LYMPHOID ORGANS; T-LYMPHOCYTES; DIFFERENTIAL REGULATION; SIGNAL-TRANSDUCTION; CUTTING EDGE; INTERNALIZATION;
D O I
10.4049/jimmunol.177.4.2314
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The chemokine receptor CCR7 and its ligands CCL19 and CCL21 play a crucial role for the homing of lymphocytes and dendritic cells to secondary lymphoid tissues. Nevertheless, how CCR7 senses the gradient of chemokines and how migration is terminated are poorly understood. In this study, we demonstrate that CCR7(-GFP) is endocytosed into early endosomes containing transferrin receptor upon CCL19 binding, but less upon CCL21 triggering. Internalization of CCR7 was independent of lipid rafts but relied on dynamin and Eps15 and was inhibited by hypertonic sucrose, suggesting clathrin-dependent endocytosis. After chemokine removal, internalized CCR7 recycled back to the plasma membrane and was able to mediate migration again. In contrast, internalized CCL19 was sorted to lysosomes for degradation, showing opposite fate for endocytosed CCR7 and its ligand.
引用
收藏
页码:2314 / 2323
页数:10
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