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首页> 外文期刊>British Journal of Cancer >Intense tumour-cell destruction by syngeneic mice: role of macrophages, complement activation and tumour-cell factors
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Intense tumour-cell destruction by syngeneic mice: role of macrophages, complement activation and tumour-cell factors

机译:同系小鼠激烈的肿瘤细胞破坏:巨噬细胞,补体激活和肿瘤细胞因子的作用

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摘要

When injected i.p. and in large numbers (10(7)) into syngeneic mice, 125IUdR-labelled L1210 cells are rapidly destroyed in a small proportion of animals, while in the other animals the lysis is low. This bimodal distribution is clearly visible 24 h after cell injection. The intense lysis occurs in fewer animals when macrophage-derived lysosomal enzymes are inhibited by trypan blue and if the complement is depleted by high doses of cobra venom factor (CVF). The intense destruction occurs in more animals after adjuvant treatment, if the mice are latently contaminated, after a moderate production of C3b by low doses of CVF, or after the injection of a tumour-cell dialysate. The destruction seems to be the result of positive feedback reaction which involves at least macrophages and complement activation.
机译:注射时。并且大量(10(7))进入同胞小鼠中,125iUDR标记的L1210细胞在少量的动物中迅速破坏,而在其他动物中,裂解低。细胞注射后24小时清晰可见这种双峰分布。当巨噬细胞衍生的溶酶体酶被Trypan蓝色抑制并且如果通过高剂量的眼镜蛇毒液因子(CVF)耗尽时,激烈的裂解发生在更少的动物中。如果小鼠通过低剂量的CVF或注射肿瘤细胞透析液,则在佐剂治疗后,在佐剂治疗后发生的促进在佐剂治疗后发生的强烈破坏。破坏似乎是阳性反馈反应的结果,涉及至少巨噬细胞和补体激活。

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