Delmas Yahsou, Viallard Jean-François, Villeneuve Julien, Grosset Christophe, Pasquet Jean-Max, Déchanet-Merville Julie, Nurden Paquita, Pellegrin Jean-Luc, Rosenbaum Jean, Combe Christian, Nurden Alan T, Ripoche Jean
GREF Inserm E362, IFR 66, Université de Bordeaux 2 et Département de Néphrologie, Hôpital Pellegrin, France.
Med Sci (Paris). 2005 Oct;21(10):825-31. doi: 10.1051/medsci/20052110825.
Blood platelets play a crucial part in the blood clotting process by forming the platelet plug. Recent evidence indicates that they are likely to play a key role in the inflammatory reaction via CD154/CD40 interactions. CD40 was known to be widely expressed, for instance on cells of the vasculature including endothelial cells, smooth muscle cells and macrophages. It was also known that the triggering of CD40 on these cells led to the acquisition of an activated pro-inflammatory and pro-coagulant phenotype. It was subsequently shown that platelets express CD154 which is cryptic in unstimulated platelets but is expressed at the platelet surface upon platelet activation. When expressed at the platelet surface and exposed to CD40-expressing vascular cells, the platelet-associated CD154 triggers a variety of pro-inflammatory and pro-coagulant responses including induction of adhesion receptors, release of cytokines and chemokines, induction of tissue factor and of metalloproteinases. Platelet-associated CD154 is also involved in platelet/platelet interactions during platelet aggregation. Furthermore, in vivo models have emphasized the critical role of the platelet-associated CD154 in the progression of atherosclerotic disease and in the stabilization of arterial thrombi. Recent data show that CD40-bearing cells involved in fibrosis such as hepatic stellate cells and glomerular mesangial cells also respond to platelet-associated CD154, thus suggesting a new mechanism by which platelets may be instrumental in the inflammatory diseases of the liver or the kidney. Finally, platelet-associated CD154 has been shown to have immune competence both in vitro and in vivo, observations that open new fields of research on the potential implications of platelets in the immune response and auto-immune diseases.
血小板通过形成血小板栓子在血液凝固过程中发挥关键作用。最近的证据表明,它们可能通过CD154/CD40相互作用在炎症反应中起关键作用。已知CD40广泛表达,例如在包括内皮细胞、平滑肌细胞和巨噬细胞在内的脉管系统细胞上。还已知这些细胞上CD40的激活会导致获得活化的促炎和促凝血表型。随后发现血小板表达CD154,其在未受刺激的血小板中是隐蔽的,但在血小板活化时在血小板表面表达。当在血小板表面表达并暴露于表达CD40的血管细胞时,血小板相关的CD154会引发多种促炎和促凝血反应,包括诱导黏附受体、释放细胞因子和趋化因子、诱导组织因子和金属蛋白酶。血小板相关的CD154也参与血小板聚集过程中的血小板/血小板相互作用。此外,体内模型强调了血小板相关的CD154在动脉粥样硬化疾病进展和动脉血栓稳定中的关键作用。最近的数据表明,参与纤维化的含CD40细胞,如肝星状细胞和肾小球系膜细胞,也对血小板相关的CD154作出反应,从而提示血小板可能在肝脏或肾脏的炎症性疾病中起作用的一种新机制。最后,血小板相关的CD154已被证明在体外和体内均具有免疫活性,这些观察结果为血小板在免疫反应和自身免疫性疾病中的潜在影响开辟了新的研究领域。