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天然巨噬细胞对阴道毛滴虫的细胞毒性由可溶性溶解因子介导。

Natural macrophage cytotoxicity against Trichomonas vaginalis is mediated by soluble lytic factors.

作者信息

Martinotti M G, Cofano F, Martinetto P, Landolfo S

出版信息

Infect Immun. 1983 Sep;41(3):1144-9. doi: 10.1128/iai.41.3.1144-1149.1983.

Abstract

Mechanisms of lysis of the extracellular protozoan Trichomonas vaginalis by uninduced resident macrophages were analyzed. Supernatants obtained by culturing such macrophages with T. vaginalis were cytotoxic for the protozoa in a dose-dependent manner. Supernatants from macrophages cultured alone were cytotoxic at lower levels, whereas those obtained from T. vaginalis alone and from macrophages cultured with unrelated cells (B77) were not cytotoxic. Cytotoxic activity appeared after 4 h of contact between effectors and target cells and reached a plateau at 18 to 24 h. Microtubule disrupting agents (colchicine and vinblastine) enhanced protozoan lysis, whereas cytochalasin B, an inhibitor of microfilaments, completely blocked T. vaginalis lysis. Treatment of macrophages with protein synthesis inhibitors (cycloheximide and puromycin) impaired effector cytotoxicity. Lytic activity remained after dialysis of supernatants, treatment with 10% bovine fetal serum, and treatment at 56 degrees C for 1 h, but it was completely prevented by treatment at 90 degrees C for 10 min. In conclusion, our data show that natural cytotoxicity against T. vaginalis is performed by normal resident macrophages through the release of at least two heterogeneous soluble factors.

摘要

分析了未诱导的驻留巨噬细胞对细胞外原生动物阴道毛滴虫的裂解机制。将此类巨噬细胞与阴道毛滴虫共同培养获得的上清液对该原生动物具有剂量依赖性的细胞毒性。单独培养的巨噬细胞的上清液细胞毒性较低,而单独从阴道毛滴虫以及与无关细胞(B77)共同培养的巨噬细胞获得的上清液则无细胞毒性。效应细胞与靶细胞接触4小时后出现细胞毒性活性,并在18至24小时达到平台期。微管破坏剂(秋水仙碱和长春碱)增强了原生动物的裂解,而微丝抑制剂细胞松弛素B则完全阻断了阴道毛滴虫的裂解。用蛋白质合成抑制剂(环己酰亚胺和嘌呤霉素)处理巨噬细胞会损害效应细胞的细胞毒性。上清液经透析、用10%胎牛血清处理以及在56℃处理1小时后,裂解活性仍然存在,但在90℃处理10分钟则完全阻止了裂解活性。总之,我们的数据表明,正常驻留巨噬细胞通过释放至少两种异质性可溶性因子对阴道毛滴虫发挥天然细胞毒性作用。

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本文引用的文献

9
The macrophage as an effector cell.作为效应细胞的巨噬细胞。
N Engl J Med. 1980 Sep 11;303(11):622-6. doi: 10.1056/NEJM198009113031106.

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