Arizono N, Nishimukai H, Nakao S, Takeoka O
Department of Pathology, Shiga University of Medical Science, Ohtsu, Japan.
Agents Actions. 1988 Jun;24(1-2):73-9. doi: 10.1007/BF01968082.
The effects of normal sera from humans, rats, and guinea pigs on unsensitized rat peritoneal mast cells were studied in vitro. Five to 20% fresh human sera induced mast cell death and substantial histamine release. The factor was heat labile. Neither hereditary C3-deficient sera nor experimentally C1q-depleted sera showed cytotoxicity. The CH50 activity of human serum was decreased to about one half after a 15-min incubation with 2 X 10(6) mast cells/ml at 37 degrees C. The cytotoxic activity and CH50 reduction were completely eliminated by an addition of 10 mM Mg-EGTA to the serum. These data demonstrated that unsensitized rat mast cells served as both the initiator and target of complement activity when human serum was used as a complement source. Requirements of both Ca++ and C1q suggested the activation of the classical pathway of complement. Fresh 5-20% sera from rats and guinea pigs, on the other hand, showed neither cytotoxicity nor CH50 reduction. Furthermore, these sera strongly inhibited the human serum-induced reaction. The latter results indicated the presence of a modulating factor in rat and guinea pig sera, which inhibits mast cell associated complement activation.
研究了人、大鼠和豚鼠的正常血清对未致敏大鼠腹膜肥大细胞的体外作用。5%至20%的新鲜人血清可诱导肥大细胞死亡并导致大量组胺释放。该因子对热不稳定。遗传性C3缺陷血清和实验性C1q缺失血清均未显示出细胞毒性。在37℃下,将人血清与2×10⁶个肥大细胞/毫升孵育15分钟后,其CH50活性降至约一半。向血清中添加10 mM Mg-EGTA可完全消除细胞毒性活性和CH50降低。这些数据表明,当使用人血清作为补体来源时,未致敏的大鼠肥大细胞既是补体活性的启动者又是靶点。对Ca++和C1q的需求表明补体经典途径被激活。另一方面,大鼠和豚鼠的新鲜5%至20%血清既未显示细胞毒性,也未导致CH50降低。此外,这些血清强烈抑制人血清诱导的反应。后一结果表明大鼠和豚鼠血清中存在一种调节因子,可抑制肥大细胞相关的补体激活。