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用钙离子载体和佛波酯刺激的B细胞系及脾B细胞分泌白细胞介素。

Interleukin secretion by B cell lines and splenic B cells stimulated with calcium ionophore and phorbol ester.

作者信息

Taira S, Matsui M, Hayakawa K, Yokoyama T, Nariuchi H

机构信息

Department of Allergology, University of Tokyo, Japan.

出版信息

J Immunol. 1987 Nov 1;139(9):2957-64.

PMID:3117882
Abstract

A B cell lymphoma A20.2J and splenic B cells produced an active material to support the proliferation of an interleukin 2 (IL-2)-dependent T cell line, CTLL-2, by stimulation with both calcium ionophore A23187 and phorbol myristate acetate (PMA). Although the production of the active material was induced by stimulation with A23187 alone in A20.2J cells, both A23187 and PMA were essential for the stimulation of splenic B cells. Neither A20.2J cells nor splenic B cells produced the active material by stimulation with PMA alone. The production was inversely proportional to the concentration of fetal calf serum in culture medium. The active material produced by B cells was indicated to be IL-2 and not B cell-stimulating factor 1 (BSF-1) for the following reasons: 1) the proliferation of CTLL-2 cells in the presence of active material was inhibited by the inclusion of anti-IL-2 receptor or anti-IL-2 in culture medium but not by anti-BSF-1; 2) the material showed no co-mitogenic activity to purified splenic B cells with anti-immunoglobulins and did not support the proliferation of FDC-P2 which are known to grow in the presence of BSF-1; and 3) IL-2 mRNA could be detected in A20.2J and splenic B cells stimulated with A23187 and PMA in Northern blot analysis. Some B cell hybridomas were also shown to produce IL-2 by similar stimulation to A20.2J. Splenic B cells as well as A20.2J cells were able to produce IL-2 by stimulation with anti-immunoglobulins. These results suggest that under certain conditions IL-2 can be produced by splenic B cells, at least some subsets of B cells, and B cell lines.

摘要

一种B细胞淋巴瘤A20.2J和脾B细胞产生了一种活性物质,通过钙离子载体A23187和佛波酯肉豆蔻酸酯(PMA)刺激,该活性物质可支持白细胞介素2(IL-2)依赖性T细胞系CTLL-2的增殖。虽然在A20.2J细胞中单独用A23187刺激可诱导活性物质的产生,但A23187和PMA对脾B细胞的刺激都是必不可少的。单独用PMA刺激时,A20.2J细胞和脾B细胞均不产生活性物质。该活性物质的产生与培养基中胎牛血清的浓度成反比。B细胞产生的活性物质被证明是IL-2而非B细胞刺激因子1(BSF-1),原因如下:1)在活性物质存在的情况下,CTLL-2细胞的增殖受到培养基中抗IL-2受体或抗IL-2的抑制,但不受抗BSF-1的抑制;2)该物质对用抗免疫球蛋白处理的纯化脾B细胞没有协同促有丝分裂活性,也不支持已知在BSF-1存在下生长的FDC-P2的增殖;3)在Northern印迹分析中,用A23187和PMA刺激的A20.2J细胞和脾B细胞中可检测到IL-2 mRNA。一些B细胞杂交瘤经与A20.2J类似的刺激也显示能产生IL-2。脾B细胞以及A20.2J细胞在用抗免疫球蛋白刺激时能够产生IL-2。这些结果表明,在某些条件下,脾B细胞、至少某些B细胞亚群和B细胞系能够产生IL-2。

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