E26转化特异性家族转录因子Spi-C在B细胞中受外部信号的动态调节

Q3 Medicine ImmunoHorizons Pub Date : 2022-01-01 DOI:10.4049/immunohorizons.2100111
Hannah L Raczkowski, Li S Xu, Wei Cen Wang, Rodney P Dekoter
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引用次数: 0

摘要

Spi-C是一种与PU.1和Spi-B密切相关的E26转化特异性转录因子。Spi-C在B细胞发育、Ab生成反应和红髓巨噬细胞生成中具有重要的谱系指导功能。本研究检测了Spi-C在小鼠B细胞中的表达调控。为了确定Spic调控的机制,我们鉴定了Spic启动子和上游调控元件。Spic启动子具有单向活性,但由于NF-κB结合位点的突变而降低。逆转录定量PCR分析显示,用细胞因子BAFF+IL-4+IL-5、抗IgM-Ab或LPS处理后,B细胞中Spic的表达减少。细胞松弛素治疗部分阻止了Spic的下调。未刺激的B细胞在培养时上调Spic。Spic被与血红素结合调节因子Bach2相互作用的上游调节区抑制。总之,这些数据表明Spi-C在B细胞中受到外部信号的动态调节,并提供了对调节机制的深入了解。
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The E26 Transformation-Specific Family Transcription Factor Spi-C Is Dynamically Regulated by External Signals in B Cells.

Spi-C is an E26 transformation-specific transcription factor closely related to PU.1 and Spi-B. Spi-C has lineage-instructive functions important in B cell development, Ab-generating responses, and red pulp macrophage generation. This research examined the regulation of Spi-C expression in mouse B cells. To determine the mechanism of Spic regulation, we identified the Spic promoter and upstream regulatory elements. The Spic promoter had unidirectional activity that was reduced by mutation of an NF-κB binding site. Reverse transcription-quantitative PCR analysis revealed that Spic expression was reduced in B cells following treatment with cytokines BAFF + IL-4 + IL-5, anti-IgM Ab, or LPS. Cytochalasin treatment partially prevented downregulation of Spic. Unstimulated B cells upregulated Spic on culture. Spic was repressed by an upstream regulatory region interacting with the heme-binding regulator Bach2. Taken together, these data indicate that Spi-C is dynamically regulated by external signals in B cells and provide insight into the mechanism of regulation.

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3.70
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