Hayashi H, Hirashima M, Honda M, Ishida M
Acta Pathol Jpn. 1978 Sep;28(5):677-88. doi: 10.1111/j.1440-1827.1978.tb00907.x.
Three different macrophage chemotactic factors were separated from hypersensitivity skin lesions induced by DNP-ascaris extract or PPD. The amount of each factor seemed to be changeable according to the nature of inflammatory stimuli. The chemotactic activity of the factor a was completely absorbed by anti-IgG and anti-light chain antibodies, while that of the factors b and c was not absorbed by the antibodies. The factor a was produced from IgG by neutrophil neutral serine protease resembling elastase but failing to digest elastin-orcein; its chemotactic generation was accompanied by release of dialysable peptide(s) from the IgG molecule, suggesting a minor structural change of the IgG molecule. Production of leucoegresin or lymphocyte chemotactic factor by neutrophil neutral thiol protease from IgG molecule was discussed.
从由二硝基苯-蛔虫提取物或结核菌素纯蛋白衍生物诱导的超敏性皮肤损伤中分离出三种不同的巨噬细胞趋化因子。每种因子的量似乎会根据炎症刺激的性质而变化。因子a的趋化活性被抗IgG和抗轻链抗体完全吸收,而因子b和c的趋化活性不被这些抗体吸收。因子a是由类似于弹性蛋白酶但不能消化弹性蛋白-orcein的中性粒细胞中性丝氨酸蛋白酶从IgG产生的;其趋化生成伴随着可透析肽从IgG分子的释放,表明IgG分子发生了微小的结构变化。还讨论了中性粒细胞中性巯基蛋白酶从IgG分子产生白细胞趋化素或淋巴细胞趋化因子的情况。