Steeber Douglas A, Venturi Guglielmo M, Tedder Thomas F
Department of Biological Sciences, Box 413, University of Wisconsin-Milwaukee, Milwaukee, WI 53201, USA.
Trends Immunol. 2005 Jan;26(1):9-12. doi: 10.1016/j.it.2004.11.012.
Leukocyte migration from blood into lymphoid and non-lymphoid tissues requires a highly orchestrated series of adhesive and signaling events. A network of adhesion molecules with overlapping functions mediate the capture, rolling and firm adhesion of leukocytes to the vascular endothelium. A new study adds a novel twist to this paradigm by demonstrating that two adhesion molecules, CD44 and VLA-4, must be physically associated with each other on activated T cells to mediate efficient rolling and firm adhesion.
白细胞从血液迁移至淋巴组织和非淋巴组织需要一系列高度协调的黏附及信号传导事件。一个具有重叠功能的黏附分子网络介导白细胞与血管内皮的捕获、滚动及牢固黏附。一项新研究为这一范例增添了新的变化,该研究表明,两种黏附分子CD44和VLA-4在活化T细胞上必须彼此物理关联,以介导有效的滚动和牢固黏附。