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机构地区:[1]上海医科大学肝癌研究所
出 处:《肿瘤》1998年第5期334-337,共4页Tumor
基 金:国家自然科学基金
摘 要:目的观察外源性神经节苷脂GM3、GD3对人肝癌SMMC┐7721细胞的杀伤活力的影响。方法应用3H┐TdR掺入法测定GM3、GD3对巨噬细胞的细胞毒作用的影响。结果GM3、GD3对巨噬细胞短时间(45分钟)作用后,两者都对细胞毒产生双相调节,但两者调节作用相反。GM3、GD3对巨噬细胞长时间(24小时)作用后,两者均抑制细胞毒作用,GD3的抑制作用更强。结论GM3、GD3作用于巨噬细胞后对其杀伤SMMC┐7721细胞的细胞毒作用产生不同程度的抑制。Objective:The cytotoxicity mediated by macrophage treated with ganglioside GM3 and GD3 on SMMC7721 cell line were detected in this study. Methods:The effect of GM3 and GD3 on cytotoxicity of macrophage was observed by the ~3HTdR incorporation.Results:Both GM3 and GD3 showed bifunctional effects on cytotoxicity after incubating with different concentration of GM3 or GD3 for a short time(45 min). The data indicated that GM3 could reduce the cytotoxicity at the lower concentration(0.1~1 mg/L) and increase it at higher concentration(10 mg/L);GD3 expressed its function in a reverse way. Treating macrophage for a long time(24 hours),it was found that both GM3 and GD3 inhibited the cytotoxicity. However,the effect of GD3 was more efficient than GM3. Conclusion:The results suggested that GM3 and GD3 may play a role in host immune surveillance and immune destruction mediated by macrophage.
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