Interleukins and IgA synthesis. Human and murine interleukin 6 induce high rate IgA secretion in IgA-committed B cells.

Interleukins and IgA synthesis. Human and murine interleukin 6 induce high rate IgA secretion in IgA-committed B cells.
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DOI:
10.1084/jem.169.6.2133
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发表时间:
1989-06-01
期刊:
The Journal of experimental medicine
影响因子:
--
通讯作者:
McGhee JR
McGhee JR
中科院分区:
其他
文献类型:
--
作者:
Beagley KW;Eldridge JH;Lee F;Kiyono H;Everson MP;Koopman WJ;Hirano T;Kishimoto T;McGhee JR

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将新鲜分离的鼠PP B细胞与10种不同的细胞因子(包括IL-1 α、IL-2、IL-4、IL-5、IL-6、IL-7、IFN-γ、TNF-α和TGF-β)一起培养,以研究这些细胞因子在诱导IG合成中的可能作用。令人感兴趣的是,发现只有IL-5和小鼠重组(mr)和人重组(hr)IL-6增强伊加合成。mrIL-6或hrIL-6的作用大于mrIL-5。IL-6诱导循环mIgA+ PP B细胞分泌高水平的伊加(比对照增加约7倍)。重要的是发现mrIL-6对PP B细胞培养物分泌IgM或IgG的影响很小。hrIL-6也增加PP B细胞的伊加分泌,这种增强作用被山羊抗hrIL-6抗血清消除。mrIL-6不引起B细胞增殖,但诱导分泌伊加的B细胞数量急剧增加。同种型转换不是这种伊加合成显著增加的机制,因为mIgA-PP B细胞不被mrIL-6诱导分泌伊加。从这些研究中,我们得出结论,IL-6在促进PP B细胞向分泌IgA的浆细胞的终末分化中起重要作用。
Freshly isolated murine PP B cells were cultured with 10 different cytokines, including IL-1 alpha, IL-2, IL-4, IL-5, IL-6, IL-7, IFN- gamma, TNF-alpha, and TGF-beta, to investigate a possible role for these cytokines in induction of Ig synthesis. Of interest was the finding that only IL-5 and both mouse recombinant (mr) and human recombinant (hr) IL-6 enhanced IgA synthesis. The effect was greater with either mrIL-6 or hrIL-6 than with mrIL-5. IL-6 induced cycling mIgA+ PP B cells to secrete high levels of IgA (approximately 7-fold increase over control). Of importance was the finding that mrIL-6 had little effect on secretion of IgM or IgG by PP B cell cultures. hrIL-6 also increased IgA secretion by PP B cells and this enhancement was abolished by a goat anti-hrIL-6 antiserum. mrIL-6 did not cause B cell proliferation but induced a sharp increase in numbers of B cells secreting IgA. Isotype-switching was not a mechanism for this marked increase in IgA synthesis since mIgA- PP B cells were not induced to secrete IgA by mrIL-6. From these studies we conclude that IL-6 plays an important role in promoting the terminal differentiation of PP B cells to IgA-secreting plasma cells.
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