Department of Pathology, LSU Health Sciences Center-Shreveport, 1501 Kings Hwy.,Shreveport, LA 71130, United States.
Semin Cell Dev Biol. 2012 Sep;23(7):745-57. doi: 10.1016/j.semcdb.2012.05.003. Epub 2012 May 24.
Vascular growth and remodeling responses entail several complex biochemical, molecular, and cellular responses centered primarily on endothelial cell activation and function. Recent studies reveal that changes in endothelial cell redox status critically influence numerous cellular events that are important for vascular growth under different conditions. It has been known for some time that oxidative stress actively participates in many aspects of angiogenesis and vascular remodeling. Initial studies in this field were largely exploratory with minimal insight into specific molecular mechanisms and how these responses could be regulated. However, it is now clear that intracellular redox mechanisms involving hypoxia, NADPH oxidases (NOX), xanthine oxidase (XO), nitric oxide and its synthases, and intracellular antioxidant defense pathways collectively orchestrate a redox balance system whereby reactive oxygen and nitrogen species integrate cues controlling vascular growth and remodeling. In this review, we discuss key redox regulation pathways that are centrally important for vascular growth in tissue health and disease. Important unresolved questions and issues are also addressed that requires future investigation.
血管生长和重塑反应需要几个复杂的生化、分子和细胞反应,主要集中在血管内皮细胞的激活和功能上。最近的研究表明,内皮细胞氧化还原状态的变化会严重影响许多对不同条件下血管生长很重要的细胞事件。一段时间以来,人们已经知道氧化应激积极参与了血管生成和血管重塑的许多方面。该领域的早期研究主要是探索性的,对特定的分子机制以及这些反应如何被调节知之甚少。然而,现在很清楚,涉及缺氧、NADPH 氧化酶 (NOX)、黄嘌呤氧化酶 (XO)、一氧化氮及其合酶以及细胞内抗氧化防御途径的细胞内氧化还原机制共同协调了一个氧化还原平衡系统,其中活性氧和氮物种整合了控制血管生长和重塑的线索。在这篇综述中,我们讨论了对组织健康和疾病中的血管生长至关重要的关键氧化还原调节途径。还讨论了一些尚未解决的重要问题和问题,需要进一步研究。