Pankratz Susann, Bittner Stefan, Kehrel Beate E, Langer Harald F, Kleinschnitz Christoph, Meuth Sven G, Göbel Kerstin
Department of Neurology, University of Münster, 48149 Münster, Germany.
Department of Neurology, University Medical Center of the Johannes Gutenberg-University, 55131 Mainz, Germany.
Int J Mol Sci. 2016 Oct 14;17(10):1723. doi: 10.3390/ijms17101723.
Beyond their indispensable role in hemostasis, platelets have shown to affect the development of inflammatory disorders, as they have been epidemiologically and mechanistically linked to diseases featuring an inflammatory reaction in inflammatory diseases like multiple sclerosis, rheumatoid arthritis and inflammatory bowel disorders. The identification of novel molecular mechanisms linking inflammation and to platelets has highlighted them as new targets for therapeutic interventions. In particular, genetic and pharmacological studies have identified an important role for platelets in neuroinflammation. This review summarizes the main molecular links between platelets and inflammation, focusing on immune regulatory factors, receptors, cellular targets and signaling pathways by which they can amplify inflammatory reactions and that make them potential therapeutic targets.
除了在止血过程中发挥不可或缺的作用外,血小板还被证明会影响炎症性疾病的发展,因为从流行病学和机制学角度来看,它们与多发性硬化症、类风湿性关节炎和炎症性肠病等炎症性疾病中具有炎症反应的病症相关联。将炎症与血小板联系起来的新型分子机制的发现,凸显了血小板作为治疗干预新靶点的地位。特别是,遗传学和药理学研究已经确定了血小板在神经炎症中的重要作用。本综述总结了血小板与炎症之间的主要分子联系,重点关注免疫调节因子﹑受体、细胞靶点以及信号通路,通过这些因素血小板能够放大炎症反应,使其成为潜在的治疗靶点。