Chemokine requirements for B cell entry to lymph nodes and Peyer's patches

被引:398
作者
Okada, T
Ngo, VN
Ekland, EH
Förster, R
Lipp, M
Littman, DR
Cyster, JG
机构
[1] Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Howard Hughes Med Inst, San Francisco, CA 94143 USA
[3] Hannover Med Sch, Inst Immunol, D-30625 Hannover, Germany
[4] Max Delbruck Ctr Mol Med, D-13092 Berlin, Germany
[5] NYU, Med Ctr, Howard Hughes Med Inst, Skirball Inst Biomol Med, New York, NY 10016 USA
关键词
chemokine; high endothelial venule; adhesion; lymphoid organ; B cell;
D O I
10.1084/jem.20020201
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
B cell entry to lymph nodes and Peyer's patches depends on chemokine receptor signaling, but the principal chemokine involved has not been defined. Here we show that the homing of CXCR4(-/-) B cells is suppressed in CCL19 (ELC)- and CCL21 (SLC)-deficient paucity of lymph node T cells mice, but not in wild-type mice. We also find that CXCR4 can contribute to T cell homing. Using intravital microscopy, we find that B cell adhesion to high endothelial venules (HEVs) is disrupted when CCR7 and CXCR4 are predesensitized. In Peyer's patches, B cell entry is dependent on CXCR5 in addition to CCR7/CXCR4. CXCL12 (SDF1) is displayed broadly on HEVs, whereas CXCL13 (BLC) is found selectively on Peyer's patch follicular HEVs. These findings establish the principal chemokine and chemokine receptor requirements for B cell entry to lymph nodes and Peyer's patches.
引用
收藏
页码:65 / 75
页数:11
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