Department of Immunology, The Weizmann Institute of Science, Rehovot 76100, Israel.
Mol Biol Cell. 2010 Jun 1;21(11):1864-71. doi: 10.1091/mbc.e09-09-0813. Epub 2010 Apr 7.
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.
未成熟 B 细胞迁移到脾脏,在那里它们分化为成熟细胞。这个最终的成熟步骤对于使 B 细胞能够对抗原产生反应并参与免疫反应至关重要。此前,我们表明 Id2 作为一种负调节剂,可调节在脾脏中发生的未成熟 B 细胞的分化。在乳腺上皮细胞中发现 Id2 的表达依赖于 Myc-Max-Mad 转录复合物。迄今为止,几乎所有的研究都表明 Mad 蛋白通过拮抗 Myc 蛋白的功能来抑制增殖。在本研究中,我们在周围 B 细胞分化过程中跟踪 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,在未成熟 B 细胞中 Mad3 的高表达水平诱导 Id2 的表达,抑制了 B 细胞分化所必需的基因的转录。在它们分化为成熟细胞的过程中,B 细胞降低 Mad3 的表达,从而使成熟过程得以发生。