Regulation of nitric oxide production by arginine metabolic enzymes

被引:295
作者
Mori, M [1 ]
Gotoh, T [1 ]
机构
[1] Kumamoto Univ, Sch Med, Dept Mol Genet, Kumamoto 8600811, Japan
关键词
apoptosis; arginine; arginase; argininosuccinate synthetase; cationic amino acid transporter; citrulline-NO cycle; nitric oxide; nitric oxide synthase;
D O I
10.1006/bbrc.2000.3169
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. (C) 2000 Academic Press.
引用
收藏
页码:715 / 719
页数:5
相关论文
共 49 条
  • [1] ARGININE METABOLISM IN WOUNDS
    ALBINA, JE
    MILLS, CD
    BARBUL, A
    THIRKILL, CE
    HENRY, WL
    MASTROFRANCESCO, B
    CALDWELL, MD
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1988, 254 (04): : E459 - E467
  • [2] L-ARGININE TRANSPORT IS INCREASED IN MACROPHAGES GENERATING NITRIC-OXIDE
    BOGLE, RG
    BAYDOUN, AR
    PEARSON, JD
    MONCADA, S
    MANN, GE
    [J]. BIOCHEMICAL JOURNAL, 1992, 284 : 15 - 18
  • [3] N-OMEGA-HYDROXY-L-ARGININE, AN INTERMEDIATE IN THE L-ARGININE TO NITRIC-OXIDE PATHWAY, IS A STRONG INHIBITOR OF LIVER AND MACROPHAGE ARGINASE
    BOUCHER, JL
    CUSTOT, J
    VADON, S
    DELAFORGE, M
    LEPOIVRE, M
    TENU, JP
    YAPO, A
    MANSUY, D
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 203 (03) : 1614 - 1621
  • [4] L-arginine uptake, the citrulline-NO cycle and arginase II in the rat brain: an in situ hybridization study
    Braissant, O
    Gotoh, T
    Loup, M
    Mori, M
    Bachmann, C
    [J]. MOLECULAR BRAIN RESEARCH, 1999, 70 (02): : 231 - 241
  • [5] Arginase activity in endothelial cells: Inhibition by N-G-hydroxy-L-arginine during high-output NO production
    Buga, GM
    Singh, R
    Pervin, S
    Rogers, NE
    Schmitz, DA
    Jenkinson, CP
    Cederbaum, SD
    Ignarro, LJ
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1996, 271 (05): : H1988 - H1998
  • [6] Nitric oxide in excitable tissues: Physiological roles and disease
    Christopherson, KS
    Bredt, DS
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (10) : 2424 - 2429
  • [7] Closs EI, 2000, MOL PHARMACOL, V57, P68
  • [8] ACTIVATED MACROPHAGES KILL TUMOR-CELLS BY RELEASING ARGINASE
    CURRIE, GA
    [J]. NATURE, 1978, 273 (5665) : 758 - 759
  • [9] INHIBITION OF RAT-LIVER ARGINASE BY AN INTERMEDIATE IN NO BIOSYNTHESIS, N-G-HYDROXY-L-ARGININE - IMPLICATIONS FOR THE REGULATION OF NITRIC-OXIDE BIOSYNTHESIS BY ARGINASE
    DAGHIGH, F
    FUKUTO, JM
    ASH, DE
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 202 (01) : 174 - 180
  • [10] Transporters for cationic amino acids in animal cells:: Discovery, structure, and function
    Devés, R
    Boyd, CAR
    [J]. PHYSIOLOGICAL REVIEWS, 1998, 78 (02) : 487 - 545