Ronald J A, Ionescu C V, Rogers K A, Sandig M
Department of Anatomy and Cell Biology, The University of Western Ontario, London, Ontario, Canada.
J Leukoc Biol. 2001 Oct;70(4):601-9.
The adhesion molecules intercellular adhesion molecule 1 (ICAM-1) and vascular cell adhesion molecule 1 (VCAM-1) expressed in atherogenic lesions are thought to regulate monocyte diapedesis. To better understand their specific roles we used function-blocking antibodies and examined in a culture model the morphology, motility, and diapedesis of THP-1 cells interacting with human coronary artery endothelial cells. The number of motile THP-1 cells was reduced only when VCAM-1 or both ICAM-1 and VCAM-1 were blocked. Blockade of ICAM-1 and VCAM-1, either separately or together, reduced to the same degree the distance that THP-1 cells traveled. Diapedesis was reduced only during the simultaneous blockade of both adhesion molecules. Blockade of either ICAM-1 or VCAM-1 inhibited pseudopodia formation, but ICAM-1 blockade induced the formation of filopodia. We suggest that the interactions of endothelial ICAM-1 and VCAM-1 with their ligands differentially regulate distinct steps of diapedesis by modulating the ratio of active and inactive forms of small GTPases such as Rho, Rac, and Cdc42.
在动脉粥样硬化病变中表达的细胞间黏附分子1(ICAM-1)和血管细胞黏附分子1(VCAM-1)被认为可调节单核细胞渗出。为了更好地了解它们的具体作用,我们使用功能阻断抗体,并在培养模型中研究了THP-1细胞与人冠状动脉内皮细胞相互作用时的形态、运动能力和渗出情况。只有当VCAM-1或ICAM-1和VCAM-1两者均被阻断时,运动的THP-1细胞数量才会减少。单独或同时阻断ICAM-1和VCAM-1,THP-1细胞移动的距离减少程度相同。只有在同时阻断两种黏附分子时,渗出才会减少。阻断ICAM-1或VCAM-1均可抑制伪足形成,但阻断ICAM-1会诱导丝状伪足形成。我们认为,内皮ICAM-1和VCAM-1与其配体的相互作用通过调节小GTP酶(如Rho、Rac和Cdc42)的活性和非活性形式的比例,差异性地调节渗出的不同步骤。