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Role of C5a-C5aR axis in the development of atherosclerosis

机译:C5a-C5aR轴在动脉粥样硬化发展中的作用

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Complement component 5a (C5a) is a 74 amino acid glycoprotein and an important proinflammatory mediator that is cleaved enzymatically from its precursor, C5, on activation of the complement cascade. C5a is quickly metabolised by carboxypeptidases, forming the less-potent C5a desArg. C5a and C5a desArg interact with their receptors (C5aR and C5L2), which results in a number of effects which are essential to the immune response. C5a has a broad range of biological effects throughout the human body because the widespread expression of C5a receptors throughout the human organs enables C5a and C5a desArg to elicit a broad range of biological effects. Recently, accumulating evidence in humans and experimental animal models shows that the C5a-C5aR axis is involved in the development of atherosclerosis lesions. The absence or blockade of C5aRs greatly reduces the formation of atherosclerotic lesions or wire-injury-induced neointima formation in atherosclerosis-prone mice. Serum C5a level was related to the major adverse cardiovascular events in patients with advanced atherosclerosis and those with drug-eluting stent implantation. Thus, the C5a-C5aR axis may be a significant pathogenic driver of arteriosclerotic vascular disease, making C5a-C5aR inhibition an attractive therapeutic strategy.
机译:补体成分5a(C5a)是74个氨基酸的糖蛋白,是一种重要的促炎介质,在补体级联激活时会从其前体C5酶解。 C5a被羧肽酶迅速代谢,形成效力较低的C5a desArg。 C5a和C5a desArg与它们的受体(C5aR和C5L2)相互作用,从而产生许多对免疫反应必不可少的作用。 C5a在整个人体中具有广泛的生物学效应,这是因为C5a受体在整个人体器官中的广泛表达使C5a和C5a desArg能够引发广泛的生物学效应。最近,在人类和实验动物模型中积累的证据表明,C5a-C5aR轴参与了动脉粥样硬化病变的发展。 C5aRs的缺失或阻断极大地降低了易患动脉粥样硬化的小鼠中动脉粥样硬化病变的形成或导线损伤引起的新内膜的形成。血清C5a水平与晚期动脉粥样硬化患者和药物洗脱支架植入患者的主要不良心血管事件有关。因此,C5a-C5aR轴可能是动脉硬化性血管疾病的重要致病因素,使C5a-C5aR抑制成为一种有吸引力的治疗策略。

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