Cutting edge: Profile of chemokine receptor expression on human plasma cells accounts for their efficient recruitment to target tissues

被引:213
作者
Nakayama, T
Hieshima, K
Izawa, D
Tatsumi, Y
Kanamaru, A
Yoshie, O
机构
[1] Kinki Univ, Sch Med, Dept Microbiol, Osaka 5898511, Japan
[2] Kinki Univ, Sch Med, Dept Internal Med 3, Osaka 5898511, Japan
关键词
D O I
10.4049/jimmunol.170.3.1136
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We systematically examined the repertoire of chemokine receptors expressed by human plasma cells. Fresh bone marrow plasma cells and myeloma cells consistently expressed CXCR4, CXCR6, CCR10, and CCR3. Accordingly, plasma cells responded to. their respective ligands in chemotaxis and very late Ag-4-dependent cell adhesion to fibronectin. Immobilized CXC chemokine ligand (CXCL)16, a novel transmembrane-type chemokine and CXCR6 ligand, also directly induced adhesion of plasma cells without requiring G(alphai) signaling or divalent cations. Furthermore, we revealed consistent expression of CXCL12 (CXCR4 ligand), CXCL16 (CXCR6 ligand), and CC chemokine ligand 28 (CCR10 and CCR3 ligand) in tissues enriched with plasma cells including bone marrow, and constitutive expression. of CXCL12, CXCL16, and CC chemokine ligand 28 by cultured human bone marrow stromal cells. Collectively, plasma cells are likely to be recruited to bone marrow and other target tissues via CXCR4, CXCR6, CCR10, and CCR3. CXCR6 may also contribute to tissue localization of plasma cells through its direct binding to membrane-anchored CXCL16.
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收藏
页码:1136 / 1140
页数:5
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