Laboratoire Contrôle de la Réponse Immune B et des Lymphoproliférations (CRIBL), Université de Limoges, CNRS Unité Mixte de Recherche 7276, Inserm Unité 1262, Limoges, France.
Laboratoire Suivi des Thérapies Innovantes, Institut de Génétique Humaine, UMR 9002 CNRS-UM, Montpellier, France.
Cell Mol Immunol. 2023 Oct;20(10):1114-1126. doi: 10.1038/s41423-023-01069-y. Epub 2023 Aug 7.
SATB1 (Special A-T rich Binding protein 1) is a cell type-specific factor that regulates the genetic network in developing T cells and neurons. In T cells, SATB1 is required for lineage commitment, VDJ recombination, development and maturation. Considering that its expression varies during B-cell differentiation, the involvement of SATB1 needs to be clarified in this lineage. Using a KO mouse model in which SATB1 was deleted from the pro-B-cell stage, we examined the consequences of SATB1 deletion in naive and activated B-cell subsets. Our model indicates first, unlike its essential function in T cells, that SATB1 is dispensable for B-cell development and the establishment of a broad IgH repertoire. Second, we show that SATB1 exhibits an ambivalent function in mature B cells, acting sequentially as a positive and negative regulator of Ig gene transcription in naive and activated cells, respectively. Third, our study indicates that the negative regulatory function of SATB1 in B cells extends to the germinal center response, in which this factor limits somatic hypermutation of Ig genes.
SATB1(特殊 A-T 富含结合蛋白 1)是一种细胞类型特异性因子,可调节 T 细胞和神经元发育中的遗传网络。在 T 细胞中,SATB1 是谱系决定、VDJ 重组、发育和成熟所必需的。鉴于其在 B 细胞分化过程中的表达变化,需要在该谱系中阐明 SATB1 的参与。我们使用从原 B 细胞阶段删除 SATB1 的 KO 小鼠模型,检查了 SATB1 缺失对幼稚和激活 B 细胞亚群的影响。我们的模型表明,首先,与 SATB1 在 T 细胞中的必需功能不同,SATB1 对于 B 细胞发育和广泛的 IgH 库的建立是可有可无的。其次,我们表明 SATB1 在成熟 B 细胞中表现出双重功能,分别作为幼稚和激活细胞中 Ig 基因转录的正和负调节剂。第三,我们的研究表明,SATB1 在 B 细胞中的负调节功能扩展到生发中心反应,其中该因子限制了 Ig 基因的体细胞超突变。