National Defense Medical Center, Graduate Institute of Life Sciences, Taipei, Taiwan.
Genomics Research Center, Academia Sinica, Taipei, Taiwan.
Front Immunol. 2019 Aug 14;10:1909. doi: 10.3389/fimmu.2019.01909. eCollection 2019.
Regulatory B cells (Bregs) are a B cell subset that plays a suppressive role in immune responses. The CD19CD1dCD5 Bregs that can execute regulatory functions via secreting IL-10 are defined as B10 cells. Bregs suppress autoimmune and inflammatory diseases, whereas they exacerbate infectious diseases caused by bacteria, viruses, or parasites. Notably, the molecular mechanisms regulating the development and functions of Bregs are still largely unknown. Furthermore, the biological impact of Bregs in fungal infection has not yet been demonstrated. Here, we compared the gene expression profiles of IL-10-producing and -non-producing mouse splenic B cells stimulated with lipopolysaccharide (LPS) or anti-CD40 antibody. Blimp-1, a transcription factor known to be critical for plasma cell differentiation, was found to be enriched in the IL-10-producing B cells. The frequency of Blimp-1 B10 cells was increased in LPS-treated mice and in isolated B10 cells that were stimulated with LPS. Surprisingly, B cell-specific Blimp-1 knockout (Cko) mice, generated by CD19 promoter driven Cre recombinase-dependent deletion of (gene encoding Blimp-1), showed higher frequencies of B10 cells both in the steady state and following injection with LPS, as compared with control littermates. However, B10 cells lacking Blimp-1 failed to efficiently suppress the proliferation of naïve CD4 T cells primed with anti-CD3 and anti-CD28 antibodies. B10 cells can be stimulated for further differentiation into plasmablasts, and a subset of plasmablasts express IL-10. We found that B10 cells from Cko mice failed to generate both IL-10-non-producing and IL-10-producing plasmablasts. Mechanistically, we found that Blimp-1 can directly suppress , whereas, in the presence of activated STAT3, Blimp-1 works together with activated STAT3 to upregulate . Moreover, we also found that B10 cells improve the clearance of infection but worsen the infection mortality. Notably, a lack of Blimp-1 in B10 cells did not change these effects of adoptively transferred B10 cells on fungal infections. Together, our data show that Blimp-1 regulates the generation, differentiation, and IL-10 production of Bregs.
调节性 B 细胞(Bregs)是 B 细胞亚群的一种,在免疫反应中发挥抑制作用。通过分泌 IL-10 执行调节功能的 CD19+CD1d+CD5+Bregs 被定义为 B10 细胞。Bregs 可抑制自身免疫性和炎症性疾病,但会加重由细菌、病毒或寄生虫引起的传染病。值得注意的是,调节 Bregs 发育和功能的分子机制在很大程度上仍不清楚。此外,Bregs 在真菌感染中的生物学作用尚未得到证实。在这里,我们比较了经脂多糖(LPS)或抗 CD40 抗体刺激的产生和不产生 IL-10 的小鼠脾 B 细胞的基因表达谱。Blimp-1 是一种已知对浆细胞分化至关重要的转录因子,在产生 IL-10 的 B 细胞中富集。在 LPS 处理的小鼠和用 LPS 刺激的分离的 B10 细胞中,Blimp-1+B10 细胞的频率增加。令人惊讶的是,由 CD19 启动子驱动的 Cre 重组酶依赖性缺失(编码 Blimp-1 的基因)生成的 B 细胞特异性 Blimp-1 敲除(Cko)小鼠与对照同窝仔相比,在静息状态和注射 LPS 后,B10 细胞的频率更高。然而,缺乏 Blimp-1 的 B10 细胞未能有效抑制用抗 CD3 和抗 CD28 抗体诱导的幼稚 CD4 T 细胞的增殖。B10 细胞可被刺激进一步分化为浆母细胞,其中一部分浆母细胞表达 IL-10。我们发现,Cko 小鼠的 B10 细胞既不能产生产生 IL-10 的浆母细胞,也不能产生不产生 IL-10 的浆母细胞。在机制上,我们发现 Blimp-1 可以直接抑制,而在激活的 STAT3 存在下,Blimp-1 与激活的 STAT3 一起上调。此外,我们还发现 B10 细胞可改善 感染的清除,但会加重感染死亡率。值得注意的是,B10 细胞中缺乏 Blimp-1 不会改变过继转移的 B10 细胞对真菌感染的这些影响。总之,我们的数据表明,Blimp-1 调节 Bregs 的产生、分化和 IL-10 产生。