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Extracellular Signal-Regulated Protein Kinase 2 Is Required for Efficient Generation of B Cells Bearing Antigen-Specific Immunoglobulin G

机译:有效携带抗原特异性免疫球蛋白G的B细胞需要细胞外信号调节蛋白激酶2

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摘要

Activation of extracellular signal-regulated protein kinase (ERK) has been implicated in proliferation as well as differentiation in a wide variety of cell types. Using B-cell-specific gene-targeted mice, we report here that in T-cell-dependent immune responses, ERK2 is required to generate efficient immunoglobulin G (IgG) production. In its absence, the proportion of antigen-specific surface IgG1-bearing cells and the subsequent number of IgG1 antibody-secreting cells were decreased, despite apparently unimpaired class switch recombination. Notably, this defect was countered by overexpression of the antiapoptotic factor Bcl-2. Together, our results suggest that ERK2 plays a key role in efficient generation of antigen-specific IgG-bearing B cells by promoting their survival.
机译:细胞外信号调节蛋白激酶(ERK)的激活与多种细胞类型的增殖和分化有关。使用B细胞特异性基因靶向的小鼠,我们在这里报告在依赖T细胞的免疫反应中,需要ERK2才能产生有效的免疫球蛋白G(IgG)。在没有它的情况下,尽管表面开关重组显然没有受到损害,但抗原特异性表面IgG1携带细胞的比例和随后的IgG1抗体分泌细胞的数量却减少了。值得注意的是,该缺陷被抗凋亡因子Bcl-2的过度表达所抵消。在一起,我们的结果表明ERK2通过促进其存活在有效产生抗原特异性IgG的B细胞中起关键作用。

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