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Extracellular Superoxide Dismutase in Macrophages Augments Bacterial Killing by Promoting Phagocytosis

机译:巨噬细胞中的细胞外超氧化物歧化酶通过促进吞噬作用增强细菌杀伤作用。

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摘要

Extracellular superoxide dismutase (EC-SOD) is abundant in the lung and limits inflammation and injury in response to many pulmonary insults. To test the hypothesis that EC-SOD has an important role in bacterial infections, wild-type and EC-SOD knockout (KO) mice were infected with Escherichia coli to induce pneumonia. Although mice in the EC-SOD KO group demonstrated greater pulmonary inflammation than did wild-type mice, there was less clearance of bacteria from their lungs after infection. Macrophages and neutrophils express EC-SOD; however, its function and subcellular localization in these inflammatory cells is unclear. In the present study, immunogold electron microscopy revealed EC-SOD in membrane-bound vesicles of phagocytes. These findings suggest that inflammatory cell EC-SOD may have a role in antibacterial defense. To test this hypothesis, phagocytes from wild-type and EC-SOD KO mice were evaluated. Although macrophages lacking EC-SOD produced more reactive oxygen species than did cells expressing EC-SOD after stimulation, they demonstrated significantly impaired phagocytosis and killing of bacteria. Overall, this suggests that EC-SOD facilitates clearance of bacteria and limits inflammation in response to infection by promoting bacterial phagocytosis.
机译:细胞外超氧化物歧化酶(EC-SOD)在肺中含量丰富,并响应许多肺损伤而限制了炎症和损伤。为了检验EC-SOD在细菌感染中起重要作用的假说,将野生型和EC-SOD敲除(KO)小鼠感染了大肠杆菌以诱发肺炎。尽管EC-SOD KO组的小鼠比野生型小鼠表现出更大的肺部炎症,但感染后从其肺中清除细菌的情况较少。巨噬细胞和嗜中性粒细胞表达EC-SOD。然而,在这些炎性细胞中其功能和亚细胞定位尚不清楚。在本研究中,免疫金电子显微镜显示吞噬细胞的膜结合囊泡中存在EC-SOD。这些发现表明,炎症细胞EC-SOD可能在抗菌防御中起作用。为了验证这一假设,对来自野生型和EC-SOD KO小鼠的吞噬细胞进行了评估。尽管缺乏EC-SOD的巨噬细胞在刺激后比表达EC-SOD的细胞产生更多的活性氧,但它们显示出吞噬作用和细菌杀伤力明显受损。总体而言,这表明EC-SOD可通过促进细菌吞噬作用来促进细菌清除并限制感染引起的炎症。

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