Sterling H, Saginario C, Vignery A
Yale University School of Medicine, Departments of Cell Biology and Orthopaedics and Rehabilitation, New Haven, Connecticut 06510, USA.
J Cell Biol. 1998 Nov 2;143(3):837-47. doi: 10.1083/jcb.143.3.837.
Cells of the mononuclear phagocyte lineage have the capability to adhere to and fuse with each other and to differentiate into osteoclasts and giant cells. To investigate the macrophage adhesion/fusion mechanism, we focused our attention on CD44, a surface glycoprotein known to play a role in hematopoietic cell-cell adhesion. We report that CD44 expression by macrophages is highly and transiently induced by fusogenic conditions both in vitro and in vivo. We show that CD44 ligands, hyaluronic acid, chondroitin sulfates, and osteopontin prevent macrophage multinucleation. In addition, we report that the recombinant extracellular domain of CD44 binds fusing macrophages and prevents multinucleation in vitro. These data suggest that CD44 may control the mononucleated status of macrophages in tissues by virtue of mediating cell-cell interaction.
单核吞噬细胞系的细胞具有相互黏附、融合并分化为破骨细胞和巨细胞的能力。为了研究巨噬细胞的黏附/融合机制,我们将注意力集中在CD44上,它是一种已知在造血细胞间黏附中起作用的表面糖蛋白。我们报告称,巨噬细胞中CD44的表达在体外和体内均受到融合条件的高度且短暂诱导。我们发现,CD44的配体,透明质酸、硫酸软骨素和骨桥蛋白可阻止巨噬细胞多核化。此外,我们报告称,CD44的重组胞外域可结合正在融合的巨噬细胞并在体外阻止多核化。这些数据表明,CD44可能通过介导细胞间相互作用来控制组织中巨噬细胞的单核状态。