A novel chemokine receptor for SDF-1 and I-TAC involved in cell survival, cell adhesion, and tumor development

被引:1063
作者
Burns, Jennifer M.
Summers, Bretton C.
Wang, Yu
Melikian, Anita
Berahovich, Rob
Miao, Zhenhua
Penfold, Mark E. T.
Sunshine, Mary Jean
Littman, Dan R.
Kuo, Calvin J.
Wei, Kevin
McMaster, Brian E.
Wright, Kim
Howard, Maureen C.
Schall, Thomas J. [1 ]
机构
[1] ChemoCentryx Inc, Mountain View, CA 94043 USA
[2] NYU, Med Ctr, Skirball Inst Biomol Med, New York, NY 10016 USA
[3] Stanford Univ, Sch Med, Div Hematol, Stanford, CA 94305 USA
关键词
D O I
10.1084/jem.20052144
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 stromal cell-derived factor (SDF-1; also known as chemokine ligand 12 [CXCL12]) regulates many essential biological processes, including cardiac and neuronal development, stem cell motility, neovascularization, angiogenesis, apoptosis, and tumorigenesis. It is generally believed that SDF-1 mediates these many disparate processes via a single cell surface receptor known as chemokine receptor 4 (CXCR4). This paper characterizes an alternate receptor, CXCR7, which binds with high affinity to SDF-1 and to a second chemokine, interferon-inducible T cell.. chemoattractant (I-TAC; also known as CXCL11). Membrane-associated CXCR7 is expressed on many tumor cell lines, on activated endothelial cells, and on fetal liver cells, but on few other cell types. Unlike many other chemokine receptors, ligand activation of CXCR7 does not cause Ca2+ mobilization or cell migration. However, expression of CXCR7 provides cells with a growth and survival advantage and increased adhesion properties. Consistent with a role for CXCR7 in cell survival and adhesion, a specific, high affinity small molecule antagonist to CXCR7 impedes in vivo tumor growth in animal models, validating this new receptor as a target for development of novel cancer therapeutics.
引用
收藏
页码:2201 / 2213
页数:13
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