Issekutz A C, Movat K W, Movat H Z
Clin Exp Immunol. 1980 Sep;41(3):512-20.
We previously reported that the injection into rabbit skin of rabbit zymosan-activated plasma (ZAP) induces marked polymorphonuclear leucocyte (PMN) infiltration, a transient increase in vascular permeability (1 hr) and prolonged red blood cells extravasation lasting at least 10 hr. Here we describe the fractionation of ZAP to identify the factor(s) responsible for these effects. On CM Sephadex G-25 chromatography, the majority of the leucocyte-attracting, permeability-enhancing and haemorrhage-inducing activities eluted in the high-salt fractions (0 . 6 M ammonium formate, 1 M NaCl pH 5 . 0), suggesting that this is a very basic molecule(s). Furthermore, the three activities eluted in the same fraction on Sephadex G-100, with an apparent molecular weight of 14,000--17,000 daltons. These observations, and the previously described requirement for C5 in the plasma, suggest that C5ades arg is the active factor. Experiments performed in neutropenic rabbits indicated that PMN are required for both the increase in permeability and red cell extravasation. Ultrastructural studies showed extensive degenerative changes in the infiltrating PMNs evident even in 1--2-hr lesions. These ranged from 'watery' cytoplasm, loss of glycogen and cell membrane to segregation and extensive extracellular release of lysosomes. It is postulated that C5ades arg-induced chemotaxis and metabolic perturbations contribute to this rapid degeneration of the PMNs, and that the release of lysosomes from these cells results in progressive vascular injury.
我们先前报道,将兔酵母聚糖激活血浆(ZAP)注射到兔皮肤中会引起明显的多形核白细胞(PMN)浸润、血管通透性短暂增加(1小时)以及持续至少10小时的红细胞外渗延长。在此,我们描述了ZAP的分级分离,以鉴定造成这些效应的因子。在CM Sephadex G - 25柱层析上,大多数吸引白细胞、增强通透性和诱导出血的活性在高盐级分(0.6 M甲酸铵,1 M NaCl,pH 5.0)中洗脱,这表明这是一种非常碱性的分子。此外,这三种活性在Sephadex G - 100上在同一级分中洗脱,表观分子量为14,000 - 17,000道尔顿。这些观察结果,以及先前描述的血浆中对C5的需求,表明C5ades arg是活性因子。在中性粒细胞减少的兔子中进行的实验表明,通透性增加和红细胞外渗都需要PMN。超微结构研究显示,即使在1 - 2小时的损伤中,浸润的PMN也有广泛的退行性变化。这些变化包括“水样”细胞质、糖原和细胞膜的丧失,到溶酶体的分离和广泛的细胞外释放。据推测,C5ades arg诱导的趋化作用和代谢紊乱促成了PMN的这种快速退化,并且这些细胞释放溶酶体导致渐进性血管损伤。