O'Garra A, Warren D J, Holman M, Popham A M, Sanderson C J, Klaus G G
Proc Natl Acad Sci U S A. 1986 Jul;83(14):5228-32. doi: 10.1073/pnas.83.14.5228.
Recently we described a murine T-cell hybrid that produces activities that promote the differentiation of eosinophils (eosinophil differentiation factor) and cause proliferation of the BCL1 B-cell lymphoma (B-cell growth factor II activity). Both activities appear to be associated with the same molecule, which has therefore been termed interleukin 4. The hybrid does not produce any other known lymphokines. We now find that purified interleukin 4 has no effects on small resting B cells but induces naturally occurring large B cells (which have presumably been preactivated in vivo) to synthesize DNA and to secrete IgM and low levels of IgG. B cells activated by anti-Ig antibodies apparently only become responsive to the factor once they have reached late G1 stage. All bioactivities of interleukin 4 are associated with a protein of Mr 44,000 (by NaDodSO4/PAGE). Therefore these results demonstrate that this lymphokine alone is sufficient to induce clonal expansion and maturation of activated B cells.
最近,我们描述了一种小鼠T细胞杂交体,它能产生促进嗜酸性粒细胞分化的活性物质(嗜酸性粒细胞分化因子),并能引起BCL1 B细胞淋巴瘤的增殖(B细胞生长因子II活性)。这两种活性似乎都与同一分子相关,因此该分子被称为白细胞介素4。该杂交体不产生任何其他已知的淋巴因子。我们现在发现,纯化的白细胞介素4对静止的小B细胞没有影响,但能诱导天然存在的大B细胞(可能已在体内预先激活)合成DNA并分泌IgM和低水平的IgG。抗Ig抗体激活的B细胞显然只有在进入G1晚期才对该因子产生反应。白细胞介素4的所有生物活性都与一种分子量为44000的蛋白质相关(通过十二烷基硫酸钠/聚丙烯酰胺凝胶电泳)。因此,这些结果表明,这种淋巴因子单独就足以诱导活化B细胞的克隆扩增和成熟。