JANOFF A, ZWEIFACH B W
J Exp Med. 1964 Nov 1;120(5):747-64. doi: 10.1084/jem.120.5.747.
Lysosomal granules of rabbit exudate polymorphonuclear (PMN) leucocytes were isolated and then lysed by freezing-thawing. Topical application of this material to rat and rabbit mesentery produced sticking and emigration of leucocytes, stasis of blood flow, and petechial hemorrhage. The granule-free, supernatant fraction of the homogenized leucocytes failed to produce any of these reactions. Cationic proteins extracted from these granules by weak acid and precipitated by ethanol at concentrations of 20 and 45 per cent, were also tested on heterologous, homologous, and autologous mesenteric vessels. The 20 per cent ethanol-precipitated fraction produced all of the aforementioned injury reactions, whereas the 45 per cent fraction was inactive. The intensity of inflammatory changes produced by the active cationic protein fraction was greater than that produced by lysed whole granules. Both the 20 per cent and 45 per cent ethanol fractions of cationic protein induced clumping of rabbit platelets, in vitro. The 20 per cent ethanol fraction also caused a slight acceleration in rate of swelling of isolated rabbit liver mitochondria. The active material proved to be non-pyrogenic in rabbits. This material exhibited no kinin-like effects when tested on isolated smooth muscle preparations (rabbit aorta and guinea pig ileum). In the rat, the protein produced a transient vasodepression which was inhibited by pretreatment of the animal with an antihistamine. Ultraviolet absorption data and ribose assays showed that the 20 per cent ethanol fraction contained only 4 per cent or less of ribonucleic acid. Upon electrophoresis in starch gel, using acid buffer, this fraction separated into at least three major components which migrated towards the cathode. Precipitation of one of the slowly migrating components by titration of the fraction to pH 10.5 greatly increased the inflammatory activity of the material. The inflammatory basic protein fraction was essentially devoid of acid phosphatase, beta glucuronidase, acid ribonuclease, lysozyme, and catalase activity. The non-inflammatory basic protein fraction contained appreciable quantities of acid ribonuclease and lysozyme. The foregoing data demonstrate that certain of the cationic proteins present in lysosomes of rabbit exudate PMN leucocytes can reproduce one of the cardinal features of the inflammatory response; namely, adhesion and emigration of leucocytes in the microcirculation. These findings offer fresh support for the role of lysosomes in the pathogenesis of tissue injury, and may help to account for the propagation of leucocyte emigration to peak numbers during inflammatory reactions.
分离出兔渗出液多形核(PMN)白细胞的溶酶体颗粒,然后通过冻融将其裂解。将这种物质局部应用于大鼠和兔肠系膜,可导致白细胞黏附与游走、血流淤滞和瘀点性出血。匀浆白细胞的无颗粒上清液部分不会产生上述任何反应。用弱酸从这些颗粒中提取并用20%和45%浓度的乙醇沉淀的阳离子蛋白,也在异种、同种和自体肠系膜血管上进行了测试。20%乙醇沉淀部分产生了所有上述损伤反应,而45%部分无活性。活性阳离子蛋白部分产生的炎症变化强度大于裂解的整个颗粒产生的炎症变化强度。阳离子蛋白的20%和45%乙醇部分在体外均可诱导兔血小板聚集。20%乙醇部分还使分离的兔肝线粒体肿胀速率略有加快。活性物质在兔身上被证明无致热原性。在分离的平滑肌制剂(兔主动脉和豚鼠回肠)上进行测试时,该物质未表现出激肽样作用。在大鼠中,该蛋白产生短暂的血管减压作用,用抗组胺药预处理动物可抑制这种作用。紫外线吸收数据和核糖测定表明,20%乙醇部分仅含有4%或更少的核糖核酸。在酸性缓冲液中于淀粉凝胶上进行电泳时,该部分至少分离出三个向阴极迁移的主要成分。通过将该部分滴定至pH 10.5沉淀其中一个迁移缓慢的成分,可大大增加该物质的炎症活性。炎症碱性蛋白部分基本不含酸性磷酸酶、β-葡萄糖醛酸酶、酸性核糖核酸酶、溶菌酶和过氧化氢酶活性。非炎症碱性蛋白部分含有相当数量的酸性核糖核酸酶和溶菌酶。上述数据表明,兔渗出液PMN白细胞溶酶体中存在的某些阳离子蛋白可重现炎症反应的一个主要特征,即微循环中白细胞的黏附与游走。这些发现为溶酶体在组织损伤发病机制中的作用提供了新的支持,并可能有助于解释炎症反应期间白细胞游走增加至峰值数量的原因。