Visualization of the transfer reaction: Tracking immune complexes from erythrocyte complement receptor 1 to macrophages

被引:33
作者
Craig, ML [1 ]
Bankovich, AJ [1 ]
Taylor, RP [1 ]
机构
[1] Univ Virginia, Sch Med, Dept Biochem & Mol Genet, Charlottesville, VA 22908 USA
关键词
bispecific antibodies; immune-complex clearance; phagocytosis; complement receptors; monocyte-derived macrophage; innate immunity; THP-1; cell; U937;
D O I
10.1006/clim.2002.5266
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Immune complexes (IC) bound to human erythrocytes (E) via complement receptor 1 (CR1) are transferred to phagocytes in the liver and spleen. In an in vitro model system using bispecific mAb reagents (antigen-based heteropolymers) to link IC to E, we have made time-lapse movies in which fluorescently labeled IC cross the E-human macrophage interface and remain associated with the macrophage. Both these movies and fixed-time experiments reveal transfer intermediates in which IC hinge E to macrophages. Examination of model macrophages after transfer indicates that the majority of IC are on the surface at short times (2 min) but are internalized at long times (1-4 h). More than half of the surface IC colocalize with CRI. at 2 min. This evidence supports a model in which CRI-bound IC provide a secure linkage between E and macrophages, allowing rearrangements of the macrophage surface necessary for release of CR1, and IC, from the E. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:36 / 47
页数:12
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