Research Institute of Molecular Pathology (IMP), Vienna Biocenter (VBC), Vienna, Austria.
Institute of Molecular Biotechnology of the Austrian Academy of Sciences (IMBA), Vienna Biocenter (VBC), Vienna, Austria.
Front Immunol. 2022 Dec 21;13:859598. doi: 10.3389/fimmu.2022.859598. eCollection 2022.
Antibody secretion by plasma cells provides acute and long-term protection against pathogens. The high secretion potential of plasma cells depends on the unfolded protein response, which is controlled by the transcription factor Xbp1. Here, we analyzed the Xbp1-dependent gene expression program of plasma cells and identified (Mist1) as the most strongly activated Xbp1 target gene. As Mist1 plays an important role in other secretory cell types, we analyzed in detail the phenotype of Mist1-deficient plasma cells in -Cre mice under steady-state condition or upon NP-KLH immunization. Under both conditions, Mist1-deficient plasma cells were 1.4-fold reduced in number and exhibited increased IgM production and antibody secretion compared to control plasma cells. At the molecular level, Mist1 regulated a largely different set of target genes compared with Xbp1. Notably, expression of the Blimp1 protein, which is known to activate immunoglobulin gene expression and to contribute to antibody secretion, was 1.3-fold upregulated in Mist1-deficient plasma cells, which led to a moderate downregulation of most Blimp1-repressed target genes in the absence of Mist1. Importantly, a 2-fold reduction of Blimp1 () expression was sufficient to restore the cell number and antibody expression of plasma cells in -Cre mice to the same level seen in control mice. Together, these data indicate that Mist1 restricts antibody secretion by restraining Blimp1 expression, which likely contributes to the viability of plasma cells.
浆细胞通过分泌抗体为机体提供针对病原体的即刻和长期保护。浆细胞的高分泌潜能依赖未折叠蛋白反应(unfolded protein response),该反应受转录因子 Xbp1 调控。在此,我们分析了浆细胞中转录因子 Xbp1 依赖的基因表达程序,并鉴定出 (Mist1)是受 Xbp1 调控最强的靶基因之一。由于 Mist1 在其他分泌细胞类型中发挥着重要作用,我们在稳态条件下或 NP-KLH 免疫后,详细分析了 -Cre 条件性敲除 Mist1 的浆细胞的表型。在这两种情况下,Mist1 缺陷型浆细胞的数量均减少了 1.4 倍,与对照浆细胞相比,IgM 产生和抗体分泌增加。在分子水平上,Mist1 调控的靶基因与 Xbp1 有很大不同。值得注意的是,Blimp1 蛋白的表达上调了 1.3 倍,已知 Blimp1 激活免疫球蛋白基因表达并有助于抗体分泌,这导致在缺乏 Mist1 的情况下,大多数 Blimp1 抑制的靶基因的表达水平适度下调。重要的是,Blimp1 ()表达降低 2 倍足以将缺失 Mist1 的浆细胞的细胞数量和抗体表达恢复到与对照小鼠相同的水平。总之,这些数据表明 Mist1 通过限制 Blimp1 的表达来限制抗体分泌,这可能有助于浆细胞的存活。