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接种劳氏肉瘤病毒后日本鹌鹑血清中一种早期细胞毒性诱导因子的特性分析

Characterization of an early cytotoxicity-inducing factor in sera of Japanese quails after inoculation with Rous sarcoma virus.

作者信息

Yoshikawa Y, Yamanouchi K, Fukuda A, Hayami M

出版信息

Int J Cancer. 1976 Apr 15;17(4):525-32. doi: 10.1002/ijc.2910170416.

Abstract

By pre-treatment with serum of normal spleen cells used in the microcytotoxicity assay, a humoral factor which induces cytotoxic activity in normal spleen cells was demonstrated in about 40% of sera of Japanese quails as early as 3 days after inoculation with Rous sarcoma virus (RSV). This cytotoxicity-inducing activity was not present either in the IgM or the IgG fraction obtained by Sephadex gel filtration. In sera of quails with experimentally induced agammaglobulinemia, the cytotoxicity-inducing activity was demonstrated at the same frequency as in normal animals. Thus, it seems unlikely that the early cytotoxicity-inducing factor is an immunoglobulin. On the other hand, membrane fractions extracted with 3 M potassium chloride from the RSV-induced quail tumor (QT) cells used as target cells in the microcytotoxicity assay exhibited cytotoxicity-inducing activity. After spontaneous regression of an RSV-induced tumor the serum of the regressor quail contained antibodies specific to the QT cell extract. This serum removed the cytotoxicity-inducing activity of both QT cell extract and serum sampled 3 days after RSV inoculation. In contrast, serum without antibody to the QT cell extract failed to absorb the cytotoxicity-inducing activity of the extract. It is therefore suggested that soluble tumor antigens can act as an early cytotoxicity-inducing factor.

摘要

通过在微量细胞毒性试验中用正常脾细胞血清进行预处理,早在接种劳氏肉瘤病毒(RSV)3天后,在约40%的日本鹌鹑血清中就证明了一种能诱导正常脾细胞产生细胞毒性活性的体液因子。通过葡聚糖凝胶过滤获得的IgM或IgG组分中均不存在这种诱导细胞毒性的活性。在实验诱导的无丙种球蛋白血症鹌鹑的血清中,诱导细胞毒性的活性出现频率与正常动物相同。因此,早期诱导细胞毒性的因子似乎不太可能是免疫球蛋白。另一方面,在微量细胞毒性试验中用作靶细胞的RSV诱导的鹌鹑肿瘤(QT)细胞用3M氯化钾提取的膜组分表现出诱导细胞毒性的活性。RSV诱导的肿瘤自发消退后,消退鹌鹑的血清中含有针对QT细胞提取物的特异性抗体。这种血清消除了QT细胞提取物和RSV接种3天后采集的血清的诱导细胞毒性的活性。相比之下,不含针对QT细胞提取物抗体的血清未能吸收提取物的诱导细胞毒性的活性。因此,提示可溶性肿瘤抗原可作为早期诱导细胞毒性的因子。

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