Le Berre Ludmilla, Chesneau Mélanie, Danger Richard, Dubois Florian, Chaussabel Damien, Garand Mathieu, Brouard Sophie
CHU Nantes, Université de Nantes, Inserm, Centre de Recherche en Transplantation et Immunologie, UMR 1064, ITUN, Nantes, France.
Systems Biology and Immunology, Sidra Medicine, Doha, Qatar.
Front Immunol. 2021 Mar 18;12:589786. doi: 10.3389/fimmu.2021.589786. eCollection 2021.
BANK1 transcript is upregulated in whole blood after kidney transplantation in tolerant patients. In comparison to patients with rejection, tolerant patients display higher level of regulatory B cells (Bregs) expressing granzyme B (GZMB) that have the capability to prevent effector T cells proliferation. However, BANK1 was found to be decreased in these GZMB Bregs. In this article, we investigated seven different transcriptomic studies and mined the literature in order to make link between BANK1, tolerance and Bregs. As for GZMB Bregs, we found that BANK1 was decreased in other subtypes of Bregs, including IL10 and CD24CD38 transitional regulatory B cells, along with BANK1 was down-regulated in activated/differentiated B cells, as in CD40-activated B cells, in leukemia and plasma cells. Following a reductionist approach, biological concepts were extracted from BANK1 literature and allowed us to infer association between BANK1 and immune signaling pathways, as STAT1, FcγRIIB, TNFAIP3, TRAF6, and TLR7. Based on B cell signaling literature and expression data, we proposed a role of BANK1 in B cells of tolerant patients that involved BCR, IP3R, and PLCG2, and a link with the apoptosis pathways. We confronted these data with our experiments on apoptosis in total B cells and Bregs, and this suggests different involvement for BANK1 in these two cells. Finally, we put in perspective our own data with other published data to hypothesize two different roles for BANK1 in B cells and in Bregs.
在肾移植后的耐受患者全血中,BANK1转录本上调。与发生排斥反应的患者相比,耐受患者体内表达颗粒酶B(GZMB)的调节性B细胞(Bregs)水平更高,这些调节性B细胞有能力阻止效应T细胞增殖。然而,在这些GZMB+Bregs中发现BANK1减少。在本文中,我们研究了七项不同的转录组学研究并查阅文献,以建立BANK1、耐受性和Bregs之间的联系。对于GZMB+Bregs,我们发现BANK1在其他Bregs亚型中也减少,包括IL10+Bregs和CD24+CD38过渡性调节性B细胞,同时BANK1在活化/分化的B细胞中下调,如在CD40活化的B细胞、白血病细胞和浆细胞中。采用简化方法,从BANK1的文献中提取生物学概念,这使我们能够推断BANK1与免疫信号通路之间的关联,如STAT1、FcγRIIB、TNFAIP3、TRAF6和TLR7。基于B细胞信号传导文献和表达数据,我们提出BANK1在耐受患者的B细胞中发挥作用,涉及BCR、IP3R和PLCG2,并与凋亡途径存在联系。我们将这些数据与我们在总B细胞和Bregs中进行的凋亡实验数据进行对比,这表明BANK1在这两种细胞中的作用不同。最后,我们将自己的数据与其他已发表的数据相结合,推测BANK1在B细胞和Bregs中具有两种不同的作用。