Coffman T J, Cox C D, Edeker B L, Britigan B E
Department of Internal Medicine, Veterans Administration Medical Center, Iowa City, Iowa 52246.
J Clin Invest. 1990 Oct;86(4):1030-7. doi: 10.1172/JCI114805.
Tissue injury has been linked to neutrophil associated hydroxyl radical (.OH) generation, a process that requires an exogenous transition metal catalyst such as iron. In vivo most iron is bound in a noncatalytic form. To obtain iron required for growth, many bacteria secrete iron chelators (siderophores). Since Pseudomonas aeruginosa infections are associated with considerable tissue destruction, we examined whether iron bound to the Pseudomonas siderophores pyochelin (PCH) and pyoverdin (PVD) could act as .OH catalysts. Purified PCH and PVD were iron loaded (Fe-PCH, Fe-PVD) and added to a hypoxanthine/xanthine oxidase superoxide- (.O2-) and hydrogen peroxide (H2O2)-generating system. Evidence for .OH generation was then sought using two different spin-trapping agents (5.5 dimethyl-pyrroline-1-oxide or N-t-butyl-alpha-phenylnitrone), as well as the deoxyribose oxidation assay. Regardless of methodology, .OH generation was detected in the presence of Fe-PCH but not Fe-PVD. Inhibition of the process by catalase and/or SOD suggested .OH formation with Fe-PCH occurred via the Haber-Weiss reaction. Similar results were obtained when stimulated neutrophils were used as the source of .O2- and H2O2. Addition of Fe-PCH but not Fe-PVD to stimulated neutrophils yielded .OH as detected by the above assay systems. Since PCH and PVD bind ferric (Fe3+) but not ferrous (Fe2+) iron, .OH catalysis with Fe-PCH would likely involve .O2(-)-mediated reduction of Fe3+ to Fe2+ with subsequent release of "free" Fe2+. This was confirmed by measuring formation of the Fe2(+)-ferrozine complex after exposure of Fe-PCH, but not Fe-PVD, to enzymatically generated .O2-. These data show that Fe-PCH, but not Fe-PVD, is capable of catalyzing generation of .OH. Such a process could represent as yet another mechanism of tissue injury at sites of infection with P. aeruginosa.
组织损伤与中性粒细胞相关的羟基自由基(·OH)生成有关,这一过程需要外源性过渡金属催化剂,如铁。在体内,大多数铁以非催化形式结合。为了获取生长所需的铁,许多细菌会分泌铁螯合剂(铁载体)。由于铜绿假单胞菌感染与大量组织破坏有关,我们研究了与铜绿假单胞菌铁载体焦磷酸铁(PCH)和绿脓菌素(PVD)结合的铁是否能作为·OH催化剂。将纯化的PCH和PVD加载铁(Fe-PCH、Fe-PVD),并添加到次黄嘌呤/黄嘌呤氧化酶超氧化物(·O2-)和过氧化氢(H2O2)生成系统中。然后使用两种不同的自旋捕获剂(5,5-二甲基-吡咯啉-1-氧化物或N-叔丁基-α-苯基硝酮)以及脱氧核糖氧化测定法寻找·OH生成的证据。无论采用何种方法,在Fe-PCH存在下均检测到·OH生成,而Fe-PVD存在下未检测到。过氧化氢酶和/或超氧化物歧化酶对该过程的抑制表明,Fe-PCH引发的·OH形成是通过哈伯-维伊斯反应发生的。当使用刺激的中性粒细胞作为·O2-和H2O2来源时,也获得了类似结果。如上述检测系统所检测到的,向刺激的中性粒细胞中添加Fe-PCH而非Fe-PVD会产生·OH。由于PCH和PVD结合三价铁(Fe3+)而非二价铁(Fe2+),Fe-PCH催化的·OH可能涉及·O2-介导的Fe3+还原为Fe2+,随后释放“游离”Fe2+。将Fe-PCH而非Fe-PVD暴露于酶促生成的·O2-后测量Fe2+-菲咯嗪络合物的形成,证实了这一点。这些数据表明,Fe-PCH而非Fe-PVD能够催化·OH的生成。这样一个过程可能代表了铜绿假单胞菌感染部位组织损伤的又一种机制。