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线粒体呼吸复合体I调节中性粒细胞活化及肺损伤的严重程度。

Mitochondrial respiratory complex I regulates neutrophil activation and severity of lung injury.

作者信息

Zmijewski Jaroslaw W, Lorne Emmanuel, Zhao Xia, Tsuruta Yuko, Sha Yonggang, Liu Gang, Siegal Gene P, Abraham Edward

机构信息

Department of Medicine, University of Alabama at Birmingham School of Medicine, 1530 Third Avenue S, Birmingham, AL 35294-0012, USA.

出版信息

Am J Respir Crit Care Med. 2008 Jul 15;178(2):168-79. doi: 10.1164/rccm.200710-1602OC. Epub 2008 Apr 24.

Abstract

RATIONALE

Mitochondria have important roles in intracellular energy generation, modulation of apoptosis, and redox-dependent intracellular signaling. Although reactive oxygen species (ROS) participate in the regulation of intracellular signaling pathways, including activation of nuclear factor (NF)-kappaB, there is only limited information concerning the role of mitochondrially derived ROS in modulating cellular activation and tissue injury associated with acute inflammatory processes.

OBJECTIVES

To examine involvement of the mitochondrial electron transport chain complex I on LPS-mediated NF-kappaB activation in neutrophils and neutrophil-dependent acute lung injury.

METHODS

Neutrophils incubated with rotenone or metformin were treated with bacterial lipopolysaccharide (LPS) to determine the effects of mitochondrial complex I inhibition on intracellular concentrations of reactive oxygen species, NF-kappaB activation, and proinflammatory cytokine expression. Acute lung injury was produced by intratracheal injection of LPS into control, metformin, or rotenone-treated mice.

MEASUREMENTS AND MAIN RESULTS

Inhibition of complex I with either rotenone or the antihyperglycemic agent metformin was associated with increased intracellular levels of both superoxide and hydrogen peroxide, as well as inhibition of LPS-induced I kappaB-alpha degradation, NF-kappaB nuclear accumulation, and proinflammatory cytokine production. Treatment of LPS-exposed mice with rotenone or metformin resulted in inhibition of complex I in the lungs, as well as diminished severity of lung injury.

CONCLUSIONS

These results demonstrate that mitochondrial complex I plays an important role in modulating Toll-like receptor 4-mediated neutrophil activation and suggest that metformin, as well as other agents that inhibit mitochondrial complex I, may be useful in the prevention or treatment of acute inflammatory processes in which activated neutrophils play a major role, such as acute lung injury.

摘要

理论依据

线粒体在细胞内能量生成、细胞凋亡调节以及氧化还原依赖性细胞内信号传导中发挥着重要作用。尽管活性氧(ROS)参与细胞内信号通路的调节,包括核因子(NF)-κB的激活,但关于线粒体衍生的ROS在调节与急性炎症过程相关的细胞活化和组织损伤中的作用,目前仅有有限的信息。

目的

研究线粒体电子传递链复合物I在脂多糖(LPS)介导的中性粒细胞NF-κB激活以及中性粒细胞依赖性急性肺损伤中的作用。

方法

用鱼藤酮或二甲双胍孵育中性粒细胞,然后用细菌脂多糖(LPS)处理,以确定线粒体复合物I抑制对细胞内活性氧浓度、NF-κB激活和促炎细胞因子表达的影响。通过向对照、二甲双胍或鱼藤酮处理的小鼠气管内注射LPS来诱导急性肺损伤。

测量指标和主要结果

用鱼藤酮或抗高血糖药物二甲双胍抑制复合物I与细胞内超氧化物和过氧化氢水平升高有关,同时抑制LPS诱导的IκB-α降解、NF-κB核积累和促炎细胞因子产生。用鱼藤酮或二甲双胍处理暴露于LPS的小鼠,导致肺中复合物I受到抑制,同时肺损伤严重程度减轻。

结论

这些结果表明线粒体复合物I在调节Toll样受体4介导的中性粒细胞活化中起重要作用,并提示二甲双胍以及其他抑制线粒体复合物I的药物可能有助于预防或治疗以活化中性粒细胞起主要作用的急性炎症过程,如急性肺损伤。

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