Hunt J D, Ward P A
Inflammation. 1979 Jul;3(3):203-14. doi: 10.1007/BF00914177.
Rat neutrophils, alveolar macrophages, and peritoneal macrophages each released chemotactic factor inactivator (CFI) activities under conditions of endocytosis (uptake of opsonized zymosan particles and preformed immune complexes). CFI activities in supernatant fluids from phagocytizing leukocytes were found for the chemotactic factors from the third (C3) and the fifth (C5) components of complement and for the bacterial chemotactic factor (present in culture supernatant fluids from Escherichia coli.) CFI activity could also be demonstrated in homogenates obtained from disrupted leukocytes. CFI release from intact leukocytes was dependent on the duration of incubation of leukocytes with the phagocytic stimulus. No quantitative relationships were noted between the amount of CFI activity and the amount of beta-glucuronidase in phagocytic supernatant fluids released from leukocytes. The release of CFI activities from phagocytizing leukocytes may represent a regulatory ("turn-off") mechanism for the inflammatory response.
在胞吞作用(摄取调理酵母聚糖颗粒和预先形成的免疫复合物)条件下,大鼠中性粒细胞、肺泡巨噬细胞和腹腔巨噬细胞均释放趋化因子灭活剂(CFI)活性。在吞噬白细胞的上清液中发现了针对补体第三(C3)和第五(C5)成分的趋化因子以及细菌趋化因子(存在于大肠杆菌培养上清液中)的CFI活性。在破碎白细胞获得的匀浆中也可证明CFI活性。完整白细胞释放CFI取决于白细胞与吞噬刺激物孵育的持续时间。在白细胞释放的吞噬上清液中,未发现CFI活性量与β-葡萄糖醛酸酶量之间存在定量关系。吞噬白细胞释放CFI活性可能代表炎症反应的一种调节(“关闭”)机制。