Connexins in atherosclerosis.

Christos E Chadjichristos, Jean-Paul Derouette, Brenda R Kwak
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引用次数: 25

Abstract

Remodeling of the vascular wall plays a central role in many physiological processes, but also in the pathogenesis of cardiovascular diseases such as atherosclerosis and restenosis. Atherosclerosis represents the major cause of death and disability in adult populations of Western societies. Angioplasty is a common and effective method of treatment for coronary atherosclerosis, but restenosis after the procedure continues to be a serious clinical complication. The development of atherosclerosis and restenosis involves complex patterns of interactions between the dysfunctional endothelium, inflammatory cells and smooth muscle cells in which cytokines and growth factors are known to play a critical role. Apart from paracrine cell-to-cell signaling, a role for gap-junction-mediated intercellular communication has recently been suggested. In this chapter, we summarize existing evidence supporting such a role. Thus, the pattern of vascular connexins is altered during atherosclerotic plaque formation and in restenosis. In addition, disturbances in flow, inflammation and smooth muscle cell activation and proliferation have been shown to affect connexin expression or gap junctional communication. Finally, genetically modified connexin expression alters the course of these diseases in mice. Further studies will tell us whether future treatment of atherosclerosis or restenosis may involve connexin-based strategies.

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动脉粥样硬化中的连接蛋白。
血管壁的重塑在许多生理过程中起着核心作用,同时也是动脉粥样硬化和再狭窄等心血管疾病的发病机制之一。动脉粥样硬化是西方社会成年人死亡和残疾的主要原因。血管成形术是治疗冠状动脉粥样硬化的一种常见而有效的方法,但术后再狭窄仍然是一种严重的临床并发症。动脉粥样硬化和再狭窄的发展涉及功能失调的内皮细胞、炎症细胞和平滑肌细胞之间复杂的相互作用模式,已知细胞因子和生长因子在其中发挥了关键作用。除了细胞间的旁分泌信号外,最近还有人提出了间隙连接介导的细胞间通信的作用。在本章中,我们将总结支持这种作用的现有证据。因此,在动脉粥样硬化斑块形成和再狭窄过程中,血管连接蛋白的模式会发生改变。此外,血流紊乱、炎症、平滑肌细胞活化和增殖也会影响连接蛋白的表达或缝隙连接通信。最后,经基因修饰的连接蛋白表达可改变小鼠这些疾病的病程。进一步的研究将告诉我们,未来动脉粥样硬化或再狭窄的治疗是否可能涉及基于连接蛋白的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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