Brockhaus F, Brüne B
University of Erlangen-Nürnberg, Faculty of Medicine, Department of Medicine IV, Loschgestrasse 8, 91054 Erlangen, Germany.
Biochem J. 1999 Mar 1;338 ( Pt 2)(Pt 2):295-303.
Initiation of nitric oxide (NO.)-mediated apoptotic cell death in RAW 264.7 macrophages is associated with up-regulation of mitochondrial manganese superoxide dismutase (MnSOD; SOD2) and down-regulation of cytosolic copper zinc superoxide dismutase (CuZnSOD; SOD1) at their individual mRNA and protein levels. To evaluate the decreased CuZnSOD expression and the initiation of apoptosis we stably transfected macrophages to overexpress human CuZnSOD. Individual clones revealed a 2-fold increase in CuZnSOD activity. Expression of a functional and thus protective CuZnSOD was verified by attenuated superoxide (O2(.)-)-mediated apoptotic as well as necrotic cell death. In this study we showed that SOD-overexpressing macrophages (R-SOD1-12) were also protected against NO.-initiated programmed cell death. Protection was substantial towards NO. derived from exogenously added NO donors or when NO. was generated by inducible NO synthase activation, and was evident at the level of p53 accumulation, caspase activation and DNA fragmentation. Stimulation of parent and SOD-overexpressing cells with a combination of lipopolysaccharide and murine interferon gamma produced equivalent amounts of nitrite/nitrate, which ruled out attenuated inducible NO. synthase activity during protection. Because protection by a O2(.)--scavenging system during NO. -intoxication implies a role of NO. and O2(.)- in the progression of cell damage, we used uric acid to delineate the role of peroxynitrite during NO.-elicited apoptosis. The peroxynitrite scavenger uric acid left S-nitrosoglutathione or spermine-NO-elicited apoptosis unaltered, blocking only 3-morpholinosydnonimine-mediated cell death. As a result we exclude peroxynitrite from contributing, to any major extent, to NO. -mediated apoptosis. Therefore protection observed with CuZnSOD overexpression is unlikely to stem from interference with peroxynitrite formation and/or action. Unequivocally, the down-regulation of CuZnSOD is associated with NO. cytotoxicity, whereas CuZnSOD overexpression protects macrophages from apoptosis.
一氧化氮(NO.)介导的RAW 264.7巨噬细胞凋亡性细胞死亡的启动与线粒体锰超氧化物歧化酶(MnSOD;SOD2)的上调以及胞质铜锌超氧化物歧化酶(CuZnSOD;SOD1)在其各自mRNA和蛋白质水平的下调有关。为了评估CuZnSOD表达的降低和凋亡的启动,我们稳定转染巨噬细胞以过表达人CuZnSOD。各个克隆显示CuZnSOD活性增加了2倍。通过减弱超氧化物(O2(.)-)介导的凋亡以及坏死性细胞死亡,验证了功能性且具有保护作用的CuZnSOD的表达。在本研究中,我们表明超表达SOD的巨噬细胞(R-SOD1-12)也受到保护,免受NO.引发的程序性细胞死亡。对于外源性添加的NO供体产生的NO.或通过诱导型NO合酶激活产生的NO.,保护作用显著,并且在p53积累、半胱天冬酶激活和DNA片段化水平上很明显。用脂多糖和鼠干扰素γ的组合刺激亲本细胞和超表达SOD的细胞产生等量的亚硝酸盐/硝酸盐,这排除了在保护过程中诱导型NO.合酶活性减弱的可能性。因为在NO.中毒期间由O2(.)-清除系统提供的保护意味着NO.和O2(.)-在细胞损伤进展中的作用,我们使用尿酸来阐明过氧亚硝酸盐在NO.诱导的凋亡中的作用。过氧亚硝酸盐清除剂尿酸使S-亚硝基谷胱甘肽或精胺-NO诱导的凋亡保持不变,仅阻断3-吗啉代-sydnonimine介导的细胞死亡。结果,我们排除了过氧亚硝酸盐在很大程度上参与NO.介导的凋亡。因此,观察到的CuZnSOD过表达的保护作用不太可能源于对过氧亚硝酸盐形成和/或作用的干扰。明确地说,CuZnSOD的下调与NO.细胞毒性有关,而过表达CuZnSOD可保护巨噬细胞免于凋亡。