Laboratory of Molecular Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892.
J Immunol. 2013 Dec 15;191(12):5984-92. doi: 10.4049/jimmunol.1300611. Epub 2013 Nov 15.
Bcl-3 is an atypical member of the family of IκB proteins. Unlike the classic members, Bcl-3 functions as a nuclear transcriptional cofactor that may, depending on context, promote or suppress genes via association with p50/NF-κB1 or p52/NF-κB2 homodimers. Bcl-3 is also an oncogene, because it is a partner in recurrent translocations in B cell tumors, resulting in deregulated expression. Bcl-3 functions, however, remain poorly understood. We have investigated the role of Bcl-3 in B cells and discovered a previously unknown involvement in the splenic development of these cells. Loss of Bcl-3 in B cells resulted in significantly more marginal zone (MZ) and fewer follicular (FO) B cells. Conversely, transgenic expression of Bcl-3 in B cells generated fewer MZ and more FO B cells. Both Bcl-3(-/-) FO and MZ B cells were more responsive to LPS stimulation compared with their wild-type counterparts, including increased proliferation. By contrast, Bcl-3(-/-) FO B cells were more prone to apoptosis upon BCR stimulation, also limiting their expansion. The data reveal Bcl-3 as a regulator of B cell fate determination, restricting the MZ path and favoring the FO pathway, at least in part, via increased signal-specific survival of the latter, a finding of relevance to its tumorigenic activity.
Bcl-3 是 IκB 蛋白家族的一种非典型成员。与经典成员不同,Bcl-3 作为核转录共因子发挥作用,根据具体情况,通过与 p50/NF-κB1 或 p52/NF-κB2 同源二聚体的结合,促进或抑制基因。Bcl-3 也是一种癌基因,因为它是 B 细胞肿瘤中反复易位的伙伴,导致其表达失控。然而,Bcl-3 的功能仍知之甚少。我们研究了 Bcl-3 在 B 细胞中的作用,发现了其在这些细胞脾脏发育中的一个先前未知的参与。B 细胞中 Bcl-3 的缺失导致更多的边缘区 (MZ) 和更少的滤泡 (FO) B 细胞。相反,Bcl-3 在 B 细胞中的转基因表达导致更少的 MZ 和更多的 FO B 细胞。与野生型相比,Bcl-3(-/-)FO 和 MZ B 细胞对 LPS 刺激的反应更敏感,包括增殖增加。相比之下,Bcl-3(-/-)FO B 细胞在 BCR 刺激下更容易发生凋亡,也限制了它们的扩增。这些数据表明 Bcl-3 是 B 细胞命运决定的调节剂,通过增加后者的信号特异性存活,限制 MZ 途径并有利于 FO 途径,至少部分是这样,这一发现与其致瘤活性有关。