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动脉粥样硬化中的连接蛋白

Connexins in atherosclerosis.

作者信息

Chadjichristos Christos E, Derouette Jean-Paul, Kwak Brenda R

机构信息

Division of Cardiology, Department of Internal Medicine, University Hospital Geneva, Geneva, Switzerland.

出版信息

Adv Cardiol. 2006;42:255-267. doi: 10.1159/000092574.

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.

摘要

血管壁重塑在许多生理过程中起着核心作用,在动脉粥样硬化和再狭窄等心血管疾病的发病机制中也起着核心作用。动脉粥样硬化是西方社会成年人群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且有效的方法,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,其中细胞因子和生长因子已知起着关键作用。除了旁分泌细胞间信号传导外,最近有人提出间隙连接介导的细胞间通讯也发挥作用。在本章中,我们总结了支持这一作用的现有证据。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,已表明血流紊乱、炎症以及平滑肌细胞的激活和增殖会影响连接蛋白的表达或间隙连接通讯。最后,基因改造的连接蛋白表达会改变小鼠这些疾病的进程。进一步的研究将告诉我们,未来对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。

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