白细胞的非氧化抗菌反应。

J K Spitznagel
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引用次数: 79

摘要

越来越多的证据支持这一假设,即pmn和肺泡巨噬细胞具有独立于分子氧存在的抗菌机制,可以有效地对抗一系列细菌和一些真菌。嗜酸性粒细胞对血吸虫和旋毛虫幼虫具有毒性作用。在所有情况下,分离的抗菌物质都是阳离子蛋白,并且在pmn中,与pmn的azurophil细胞质颗粒相关。到目前为止,这些物质中有几种已被证明没有酶功能。其中两种物质是丝氨酸蛋白酶,但其中一种是凝乳胰蛋白酶样蛋白质,其抗菌作用取决于蛋白质的阳离子性质,与该物质的蛋白水解作用无关。在大多数情况下,由于精氨酸的比例相对较大,这些蛋白质是阳离子的。在两种情况下,存在大量赖氨酸。它们都含有高比例(约50%)的疏水氨基酸。这种蛋白存在于人、兔、豚鼠、大鼠、牛和鸡的pmn中。目前的观点是,它们对革兰氏阴性菌最有效。其中至少有两种-37-kd和57-kd蛋白(Shafer和Spitznagel, 1983)作用于鼠伤寒沙门氏菌,其作用方式类似于多粘菌素B与脂质a的结合。目前已有的研究结果表明厌氧pmn具有很强的抗菌能力。这种能力是否是由于本章讨论的不依赖于o2的机制,还有待进一步确定。
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Nonoxidative antimicrobial reactions of leukocytes.

Increasingly abundant evidence supports the hypothesis that PMNs and perhaps alveolar macrophages have antimicrobial mechanisms independent of the presences of molecular oxygen for effective action against an array of bacteria and against some fungi. Eosinophils have mechanisms toxic for schistosomula and Trichinella larvae. In all instances the antimicrobial substances isolated have been cationic proteins and, in PMNs, associated with the azurophil cytoplasmic granules of the PMNs. Several of these substances have thus far demonstrated no enzymic function. Two of these substances are serine proteases but in one, chymotrypsin-like protein, the antimicrobial action depends on the cationic properties of the protein and is independent of the proteolytic action of the substance. In most instances, these proteins are cationic due to relatively large proportions of arginine. In two instances, a large proportion of lysine is present. All have high proportions (about 50%) of hydrophobic amino acid. Such proteins occur in the PMNs of man, rabbit, guinea pig, rat, cow, and chicken. The present view is that they are most active against gram-negative bacteria. At least two of them-37-kd and 57-kd proteins (Shafer and Spitznagel, 1983)-act on S. typhimurium in a manner analogous to that of polymyxin B through binding to lipid A. Currently available results shows that anaerobic PMNs have substantial antimicrobial capacity. Whether this capacity is due to the O2-independent mechanisms discussed in this chapter remains to be established with greater certainty.

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