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首页> 外文期刊>Molecular biology of the cell >Mad3 Negatively Regulates B Cell Differentiation in the Spleen by Inducing Id2 Expression
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Mad3 Negatively Regulates B Cell Differentiation in the Spleen by Inducing Id2 Expression

机译:Mad3通过诱导Id2表达负调节脾脏B细胞分化。

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Immature B cells migrate to the spleen where they differentiate into mature cells. This final maturation step is crucial to enable B cells to become responsive to antigens and to participate in the immune response. Previously, we showed that Id2 acts as a negative regulator of the differentiation of immature B cells occurring in the spleen. Id2 expression has been found to depend on Myc–Max–Mad transcriptional complexes in mammary epithelial cells. Nearly all studies to date have shown that Mad proteins inhibit proliferation, presumably by antagonizing the function of Myc proteins. In the current study, we followed the Mad family members during peripheral B cell differentiation. We show that Mad3 actively regulates B cell differentiation. Our results demonstrate that high expression levels of Mad3 in immature B cells induce Id2 expression, which inhibits transcription of genes essential for B cell differentiation. During their differentiation to mature cells, B cells reduce their Mad3 expression, enabling the maturation process to occur.
机译:未成熟的B细胞迁移到脾脏,然后分化为成熟细胞。最后的成熟步骤对于使B细胞对抗原具有反应能力并参与免疫反应至关重要。以前,我们表明Id2充当脾脏中未成熟B细胞分化的负调控因子。发现Id2表达取决于乳腺上皮细胞中的Myc–Max–Mad转录复合物。迄今为止,几乎所有的研究都表明,Mad蛋白可以抑制Myc蛋白的功能,从而抑制增殖。在本研究中,我们在外周B细胞分化过程中追踪了Mad家族成员。我们表明,Mad3积极调节B细胞分化。我们的结果表明,未成熟B细胞中Mad3的高表达水平诱导了Id2表达,从而抑制了B细胞分化必不可少的基因的转录。在分化为成熟细胞的过程中,B细胞会降低其Mad3表达,从而使成熟过程得以发生。

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