首页 | 本学科首页   官方微博 | 高级检索  
     


Nitric oxide diffusion to red blood cells limits extracellular,but not intraphagosomal,peroxynitrite formation by macrophages
Affiliation:2. Neurona Therapeutics, San Francisco, CA, United States;3. Massachusetts General Hospital, Harvard Medical School, Boston, MA, United States
Abstract:Macrophage-derived nitric oxide (NO) participates in cytotoxic mechanisms against diverse microorganisms and tumor cells. These effects can be mediated by NO itself or NO-derived species such as peroxynitrite formed by its diffusion-controlled reaction with NADPH oxidase-derived superoxide radical anion (O2). In vivo, the facile extracellular diffusion of NO as well as different competing consumption routes limit its bioavailability for the reaction with O2 and, hence, peroxynitrite formation. In this work, we evaluated the extent by which NO diffusion to red blood cells (RBC) can compete with activated macrophages-derived O2 and affect peroxynitrite formation yields. Macrophage-dependent peroxynitrite production was determined by boron-based probes that react directly with peroxynitrite, namely, coumarin-7-boronic acid (CBA) and fluorescein-boronate (Fl-B). The influence of NO diffusion to RBC on peroxynitrite formation was experimentally analyzed in co-incubations of NO and O2-forming macrophages with erythrocytes. Additionally, we evaluated the permeation of NO to RBC by measuring the intracellular oxidation of oxyhemoglobin to methemoglobin. Our results indicate that diluted RBC suspensions dose-dependently inhibit peroxynitrite formation, outcompeting the O2 reaction. Computer-assisted kinetic studies evaluating peroxynitrite formation by its precursor radicals in the presence of RBC are in accordance with experimental results. Moreover, the presence of erythrocytes in the proximity of NO and O2--forming macrophages prevented intracellular Fl-B oxidation pre-loaded in L1210 cells co-cultured with activated macrophages. On the other hand, Fl-B-coated latex beads incorporated in the macrophage phagocytic vacuole indicated that intraphagosomal probe oxidation by peroxynitrite was not affected by nearby RBC. Our data support that in the proximity of a blood vessel, NO consumption by RBC will limit the extracellular formation (and subsequent cytotoxic effects) of peroxynitrite by activated macrophages, while the intraphagosomal yield of peroxynitrite will remain unaffected.
Keywords:Superoxide  Nitric oxide  Peroxynitrite  Macrophages  Free radicals  Phagosome  Boronate  Kinetics
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号