Section of Pulmonary and Critical Care Medicine, Yale University School of Medicine, New Haven, CT 06520, USA.
Curr Drug Targets. 2010 Dec;11(12):1532-40. doi: 10.2174/1389450111009011532.
The lungs are a major target for various inflammatory, oxidative, carcinogenic or infectious stressors, which result in a range of lung diseases. Induction of heme oxygenase-1 (HO-1) during acute and chronic lung processes is a crucial defense mechanism. HO-1 catalyzes the degradation of free cellular heme to iron, carbon monoxide (CO) and biliverdin which is eventually converted to bilirubin by biliverdin reductase. In addition to the degradation of free heme, a pro-oxidant, HO-1 exerts anti-oxidant, anti-inflammatory and anti-apoptotic properties via its reaction products. This review summarizes the regulation and protective roles of HO-1 and its reaction products in several in vitro and in vivo lung disease models, including acute lung injury, ischemia-reperfusion (IR)-induced lung injury, cigarette smoke and chronic obstructive pulmonary disease (COPD), pulmonary arterial hypertension (PAH), lung cancer and asthma. The therapeutic applications of HO-1 in the lung as well as potential complications of excessive HO-1 induction are also covered. In summary, the HO-1 system is a powerful endogenous defense strategy with immense therapeutic potential against a range of lung diseases if optimal levels and tissue targeting can be achieved.
肺部是各种炎症、氧化、致癌或感染性应激源的主要靶标,这些应激源会导致一系列肺部疾病。在急性和慢性肺过程中诱导血红素加氧酶-1(HO-1)是一种重要的防御机制。HO-1 催化游离细胞血红素降解为铁、一氧化碳(CO)和胆绿素,胆绿素最终被胆绿素还原酶转化为胆红素。除了降解游离血红素(一种促氧化剂)外,HO-1 还通过其反应产物发挥抗氧化、抗炎和抗凋亡作用。
这篇综述总结了 HO-1 及其反应产物在几种体外和体内肺疾病模型中的调节和保护作用,包括急性肺损伤、缺血再灌注(IR)诱导的肺损伤、吸烟和慢性阻塞性肺疾病(COPD)、肺动脉高压(PAH)、肺癌和哮喘。还介绍了 HO-1 在肺部的治疗应用以及过度诱导 HO-1 可能产生的潜在并发症。
总之,如果能达到最佳水平和组织靶向性,HO-1 系统是一种强大的内源性防御策略,具有治疗多种肺部疾病的巨大潜力。