Forsyth K D
Department of Immunology, Children's Hospital Medical Centre, Perth, Western Australia.
Immunology. 1991 Feb;72(2):292-6.
Anti-CD9 antibodies which bind to the CD9 (p24) antigen are known to induce platelet and pre-B-cell aggregation. We show here that human endothelium expresses the CD9 antigen, and anti-CD9 antibodies incubated with endothelium induce a rapid increase in adhesion of neutrophils to endothelium by an action on the endothelial cell. This augmented adhesion is not mediated by glycoprotein IIb/IIIa or by the leucocyte integrins. Binding of anti-CD9 antibody to CD9 induces shedding of the CD9/anti-CD9 complex off the endothelial cell in a time-dependent manner. It is likely that CD9 binding to its ligand induces an activation event within the endothelial cell, resulting in surface expression of a pre-formed adhesive ligand for the neutrophil, or an activation change to a constitutively expressed ligand to render it functional.
已知与CD9(p24)抗原结合的抗CD9抗体可诱导血小板和前B细胞聚集。我们在此表明,人内皮细胞表达CD9抗原,与内皮细胞一起孵育的抗CD9抗体通过作用于内皮细胞诱导中性粒细胞与内皮细胞的黏附迅速增加。这种增强的黏附不是由糖蛋白IIb/IIIa或白细胞整合素介导的。抗CD9抗体与CD9的结合以时间依赖性方式诱导CD9/抗CD9复合物从内皮细胞上脱落。CD9与其配体的结合可能在内皮细胞内诱导激活事件,导致为中性粒细胞预先形成的黏附配体的表面表达,或对组成性表达的配体进行激活改变以使其具有功能。