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一种具有小B淋巴细胞生化特征的产生IgM的肿瘤。

An IgM-producing tumor with biochemical characteristics of a small B lymphocyte.

作者信息

Bergman Y, Haimovich J, Melchers F

出版信息

Eur J Immunol. 1977 Aug;7(8):574-9. doi: 10.1002/eji.1830070815.

Abstract

A lymphocytic tumor, 38C-13, induced by the chemical carcinogen 7, 12-dimethylbenz(a)anthracene in C3H/eB mice and adapted to tissue culture, produces 7-8 S IgM with "core" carbohydrates (N-acetylglucosamines, mannoses), but not "branch" carbohydrates (neuraminic acids, fucoses, galactoses) attached to the mu heavy, but not to the light chains. Turnover of the 7-8 S 38C-13 IgM is slow (half disappearance time = 10-15 h). The IgM is released from the cells as 7-8 S IgM. The ratio of IgM synthesis to the synthesis of all cellular glycoproteins is 0.005-0.01. After comparison of these data with data obtained with normal B lymphocytes before and after mitogenic stimulation, we conclude that 38C-13 tumor cells are transformed counterparts very near or within the population of small, mitogen-sensitive, resting B lymphocytes.

摘要

一种由化学致癌物7,12 - 二甲基苯并(a)蒽在C3H/eB小鼠中诱导产生并适应组织培养的淋巴细胞肿瘤38C - 13,可产生带有“核心”碳水化合物(N - 乙酰葡糖胺、甘露糖)的7 - 8S IgM,但在μ重链而非轻链上未连接“分支”碳水化合物(神经氨酸、岩藻糖、半乳糖)。7 - 8S 38C - 13 IgM的周转缓慢(半衰期 = 10 - 15小时)。IgM以7 - 8S IgM的形式从细胞中释放。IgM合成与所有细胞糖蛋白合成的比率为0.005 - 0.01。将这些数据与有丝分裂原刺激前后正常B淋巴细胞获得的数据进行比较后,我们得出结论,38C - 13肿瘤细胞是非常接近或处于小的、对有丝分裂原敏感的静止B淋巴细胞群体内的转化对应物。

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