Mori M, Gotoh T
Department of Molecular Genetics, Kumamoto University School of Medicine, Kumamoto, 860-0811, Japan.
Biochem Biophys Res Commun. 2000 Sep 7;275(3):715-9. doi: 10.1006/bbrc.2000.3169.
Nitric oxide (NO) is synthesized from arginine by NO synthase (NOS), and the availability of arginine is one of the rate-limiting factors in cellular NO production. Citrulline, which is formed as a by-product of the NOS reaction, can be recycled to arginine by successive actions of argininosuccinate synthetase (AS) and argininosuccinate lyase (AL), forming the citrulline-NO cycle. AS and sometimes AL have been shown to be coinduced with inducible NOS (iNOS) in various cell types including activated macrophages, vascular smooth muscle cells, glial cells, neuronal PC12 cells, and pancreatic beta-cells. Cationic amino acid transporter (CAT)-2 is induced in activated macrophages but not in PC12 cells. On the other hand, arginase can downregulate NO production by decreasing intracellular arginine concentrations. iNOS and arginase activities are regulated reciprocally in macrophages by cytokines, and this may guarantee the efficient production of NO. In contrast, iNOS and arginase isoforms (type I and II) are coinduced in lipopolysaccharide (LPS)-activated macrophages. These results indicate that NO production is modulated by the uptake, recycling, and degradation of arginine.
一氧化氮(NO)由一氧化氮合酶(NOS)催化精氨酸合成,精氨酸的可利用性是细胞内NO生成的限速因素之一。作为NOS反应的副产物生成的瓜氨酸,可通过精氨琥珀酸合成酶(AS)和精氨琥珀酸裂解酶(AL)的连续作用再循环为精氨酸,形成瓜氨酸-NO循环。在包括活化巨噬细胞、血管平滑肌细胞、神经胶质细胞、神经元PC12细胞和胰岛β细胞在内的多种细胞类型中,AS以及有时还有AL已被证明与诱导型NOS(iNOS)共同被诱导。阳离子氨基酸转运体(CAT)-2在活化巨噬细胞中被诱导,但在PC12细胞中不被诱导。另一方面,精氨酸酶可通过降低细胞内精氨酸浓度来下调NO生成。在巨噬细胞中,iNOS和精氨酸酶活性受细胞因子的相互调节,这可能保证了NO的高效生成。相反,iNOS和精氨酸酶同工型(I型和II型)在脂多糖(LPS)活化的巨噬细胞中共同被诱导。这些结果表明,NO生成受精氨酸的摄取、再循环和降解的调节。