Rizvi Muhammad, Pathak Didi, Freedman Jane E, Chakrabarti Subrata
Whitaker Cardiovascular Institute and Evans Department of Medicine, Boston University School of Medicine, Boston, MA 02118, USA.
Trends Mol Med. 2008 Dec;14(12):530-8. doi: 10.1016/j.molmed.2008.09.006. Epub 2008 Oct 30.
CD40 ligand (CD40L) and its receptor CD40 participate in numerous inflammatory pathways that contribute to multiple pathophysiological processes. A role for CD40-CD40L interactions has been identified in atherosclerosis, and such interactions are known to destabilize atherosclerotic plaques by inducing the expression of cytokines, chemokines, growth factors, matrix metalloproteinases and pro-coagulant factors. The CD40-CD40L interaction has also been implicated in immune system disorders. Recent studies have suggested that CD40-CD40L interactions regulate oxidative stress and affect various signaling pathways in both the immunological and cardiovascular systems. Here, we discuss the emerging role of CD40-CD40L-mediated processes in oxidative stress, inflammatory pathways and vascular diseases. Understanding the roles and regulation of CD40-CD40L-mediated oxidative signaling in immune and non-immune cells could facilitate the development of therapeutics targeting diverse inflammatory diseases.
CD40配体(CD40L)及其受体CD40参与众多炎症途径,这些途径促成多种病理生理过程。CD40-CD40L相互作用在动脉粥样硬化中所起的作用已得到确认,已知此类相互作用通过诱导细胞因子、趋化因子、生长因子、基质金属蛋白酶和促凝血因子的表达,使动脉粥样硬化斑块不稳定。CD40-CD40L相互作用也与免疫系统疾病有关。最近的研究表明,CD40-CD40L相互作用调节氧化应激,并影响免疫系统和心血管系统中的各种信号通路。在此,我们讨论CD40-CD40L介导的过程在氧化应激、炎症途径和血管疾病中正在显现的作用。了解CD40-CD40L介导的氧化信号在免疫细胞和非免疫细胞中的作用及调控,可能有助于开发针对多种炎症性疾病的治疗方法。