King Nina E, Rothenberg Marc E, Zimmermann Nives
Division of Allergy and Immunology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.
J Nutr. 2004 Oct;134(10 Suppl):2830S-2836S; discussion 2853S. doi: 10.1093/jn/134.10.2830S.
Asthma, a complex chronic inflammatory pulmonary disorder, is on the rise despite intense ongoing research underscoring the need for new scientific inquiry. Using global microarray analysis, we recently discovered that asthmatic responses involve metabolism of arginine by arginase. We found that the cationic amino acid transporter (CAT)2, arginase I, and arginase II were particularly prominent among the allergen-induced gene transcripts. These genes are key regulators of critical processes associated with asthma, including airway tone, cell hyperplasia, and collagen deposition, respectively. Recent data suggest that arginase induction is not just a marker of allergic airway responses, but that arginase is involved in the pathogenesis of multiple aspects of disease. This review focuses on the current body of knowledge on L-arginine metabolism in asthma.
哮喘是一种复杂的慢性炎症性肺部疾病,尽管目前正在进行深入研究强调需要新的科学探索,但哮喘的发病率仍在上升。通过全球微阵列分析,我们最近发现哮喘反应涉及精氨酸酶对精氨酸的代谢。我们发现阳离子氨基酸转运体(CAT)2、精氨酸酶I和精氨酸酶II在变应原诱导的基因转录物中尤为突出。这些基因分别是与哮喘相关的关键过程的关键调节因子,包括气道张力、细胞增生和胶原蛋白沉积。最近的数据表明,精氨酸酶的诱导不仅是过敏性气道反应的一个标志物,而且精氨酸酶参与了疾病多个方面的发病机制。本综述聚焦于目前关于哮喘中L-精氨酸代谢的知识体系。