Dajnowiec Dorota, Langille B Lowell
Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.
Clin Sci (Lond). 2007 Jul;113(1):15-23. doi: 10.1042/CS20060337.
Healthy mature arteries are usually extremely quiescent tissues with cell proliferation rates much below 1%/day and with extracellular matrix constituents exhibiting half-lives of years to decades. However, chronic physiological or pathological changes in haemodynamic function elicit arterial remodelling processes that may involve substantial tissue synthesis, degradation or turnover. Although these remodelling processes accommodate changing demands placed upon the cardiovascular system by physiological adaptations, they can compromise further perfusion in the context of arterial occlusive disease and they entrench hypertension and may exacerbate its progression. Recent findings indicate that some of the most important such remodelling responses involve the integrated effects of persistently altered vascular tone that feed into restructuring responses, with common signalling pathways frequently interacting in the control of both phases of the response. Current efforts to define these signals and their targets may provide new directions for therapeutic interventions to treat important vascular disorders.
健康成熟的动脉通常是极其静止的组织,细胞增殖率远低于1%/天,细胞外基质成分的半衰期长达数年至数十年。然而,血液动力学功能的慢性生理或病理变化会引发动脉重塑过程,这可能涉及大量的组织合成、降解或更新。尽管这些重塑过程能够适应生理适应对心血管系统提出的不断变化的需求,但在动脉闭塞性疾病的情况下,它们会影响进一步的灌注,还会导致高血压并可能加剧其进展。最近的研究结果表明,一些最重要的此类重塑反应涉及持续改变的血管张力的综合作用,这些作用会引发结构重塑反应,常见的信号通路在反应的两个阶段的控制中经常相互作用。目前确定这些信号及其靶点的努力可能为治疗重要血管疾病的治疗干预提供新方向。