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凝集素诱导肿瘤相关巨噬细胞介导的自体肿瘤细胞裂解

Induction of tumor associated macrophage-mediated lysis of autologous tumor cells by lectins.

作者信息

Chattopadhyay U, Bhattacharyya S

机构信息

Department of Tumor Immunobiology, Chittaranjan National Cancer Research Center, Calcutta, India.

出版信息

Neoplasma. 1988;35(3):321-8.

PMID:3405340
Abstract

Lectin dependent cell mediated cytotoxicity (LDCC) to autologous tumor cells (ATC) by the tumor associated macrophages (TAM) was studied by 4 h 51Cr release assays at early and late stages of growth of a murine transplantable ascites tumor, S-180, in presence of different concentrations of wheat germ agglutinin (WGA) and Concanavalin A (Con A). Induction of LDCC by the unstimulated resident macrophages (RM) to S-180 tumor cells was also assayed. Both WGA and Con A induced significant tumoricidal activity in the TAM at different states of activation and in RM in a dose-dependent manner, the activated TAM showing expression of cytotoxicity with the lowest doses of the lectins used. Addition of N-acetylglucosamine (NAcGle) or D-mannose (D-man) in the assay completely inhibited LDCC induced by WGA and Con A, respectively. Effector-target contact alone not sufficient for inducing lysis in LDCC was evident from the observations that low doses of the lectins augmented target binding by the inactivated TAM and RM with no subsequent cytolysis.

摘要

在小鼠可移植腹水瘤S-180生长的早期和晚期,通过4小时51Cr释放试验,研究了肿瘤相关巨噬细胞(TAM)对自体肿瘤细胞(ATC)的凝集素依赖性细胞介导的细胞毒性(LDCC),试验中存在不同浓度的麦胚凝集素(WGA)和刀豆球蛋白A(Con A)。还检测了未刺激的驻留巨噬细胞(RM)对S-180肿瘤细胞的LDCC诱导情况。WGA和Con A均以剂量依赖性方式在不同激活状态的TAM和RM中诱导出显著的杀肿瘤活性,激活的TAM在用最低剂量的凝集素时就表现出细胞毒性。在试验中分别添加N-乙酰葡糖胺(NAcGle)或D-甘露糖(D-man)可完全抑制WGA和Con A诱导的LDCC。从低剂量凝集素增强失活的TAM和RM与靶标的结合但随后没有细胞溶解的观察结果可以明显看出,在LDCC中仅效应细胞与靶细胞的接触不足以诱导细胞溶解。

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