首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Natural killing of tumor cells by human peripheral blood cells. Suppression of killing in vitro by tumor-promoting phorbol diesters.
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Natural killing of tumor cells by human peripheral blood cells. Suppression of killing in vitro by tumor-promoting phorbol diesters.

机译:人类外周血细胞自然杀死肿瘤细胞。促进肿瘤的佛波二酯抑制体外杀伤。

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摘要

Tumor-promoting phorbol diesters were shown to suppress natural killing in vitro by human peripheral blood mononuclear cells. The inhibitory effect of different phorbol diesters and their analogues correlated with their potency as tumor promoters, the most effective agent being 12-O-tetradecanoylphorbol-13-acetate (TPA). Both peripheral blood cells and targets specifically bound TPA, and natural killing could be inhibited by pretreatment of either cell population with TPA, though this was less effective than direct addition of TPA to the assay. Cells that had been pretreated with TPA released TPA and metabolites of tPA during subsequent incubation in fresh medium. This release of tPA was evidently responsible for the inhibition of natural killing by pretreated target cells; in experiments where labeled and unlabeled target cells were mixed, pretreatment of unlabeled targets with TPA inhibited killing of labeled targets. Suppression of natural killing by TPA was greatly reduced when adherent cells were removed from the peripheral blood cells, suggesting that monocytes mediate suppression. Inhibition of natural killing by TPA provides a model for examining the regulation of natural killing. Suppression of natural killing by phorbol diesters may contribute to their activity as tumor promoters.
机译:促肿瘤的佛波二酯显示出在体外抑制人外周血单核细胞的自然杀伤作用。不同的佛波二酯及其类似物的抑制作用与其作为肿瘤促进剂的效力有关,最有效的药物是12-O-十四烷酰佛波-13-乙酸酯(TPA)。外周血细胞和靶标均特异性结合TPA,并且可以通过用TPA预处理任一细胞群来抑制自然杀伤,尽管这种方法不如直接将TPA加到测定中有效。用TPA预处理的细胞在随后于新鲜培养基中孵育期间会释放TPA和tPA代谢产物。 tPA的这种释放显然是预处理靶细胞抑制自然杀伤的原因。在将标记和未标记靶细胞混合的实验中,用TPA预处理未标记靶可抑制标记靶的杀伤。当从外周血细胞中去除粘附细胞时,TPA对自然杀伤的抑制作用大大降低,表明单核细胞介导抑制作用。 TPA对自然杀伤的抑制作用为研究自然杀伤的调控提供了一个模型。佛波二酯抑制自然杀伤可能有助于其作为肿瘤促进剂的活性。

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