Activated human neutrophils rapidly break down nitric oxide

FEBS Letters

Brown, Guy C¹  McBride, Alan G¹ 

[1] Department of Biochemistry, University of Cambridge, Tennis Court Road, Cambridge CB2 1QW, UK

关键词: Neutrophils;    Nitric oxide;    Respiratory burst;    Superoxide;    cNOS;    constitutive nitric oxide synthase;    Cu/Zn-SOD;    copper/zinc superoxide dismutase;    FMLP;    N-formyl-l-methionyl-l-leucyl-l-phenylalanine;    PMA;    phorbol 12-myristate 13-acetate;   

DOI  :  10.1016/S0014-5793(97)01284-2

学科分类：生物化学/生物物理

来源: John Wiley & Sons Ltd.

【 摘 要 】

Isolated human neutrophils produced no detectable (<10 nM) nitric oxide (NO) before or after activation with phorbol 12-myristate 13-acetate (PMA) or a chemotactic peptide, N-formyl-l-methionyl-l-leucyl-l-phenylalanine. Physiological levels of NO (1 μM) added before or after neutrophil activation had no effect on their respiratory burst oxygen consumption. Neutrophils activated with PMA caused very rapid breakdown of exogenously added NO. NO breakdown rates recorded at 250 nM NO were 0.09±0.02 and 3.77±0.23 nmol NO/min/10⁶ cells (n=3) before and after activation respectively and addition of copper-zinc superoxide dismutase during activation significantly decreased this rate (1.06±0.09 nmol NO/min/10⁶ cells (n=3)), suggesting that superoxide (O⁻ ₂) production was mainly responsible for the NO breakdown. These results suggest that activation of human neutrophils in vivo will dramatically decrease surrounding NO levels, potentially causing vasoconstriction, platelet aggregation and adhesion and peroxynitrite (ONOO⁻) formation.

【 授权许可】

Unknown