Ozaki Katsutoshi, Spolski Rosanne, Ettinger Rachel, Kim Hyoung-Pyo, Wang Gang, Qi Chen-Feng, Hwu Patrick, Shaffer Daniel J, Akilesh Shreeram, Roopenian Derry C, Morse Herbert C, Lipsky Peter E, Leonard Warren J
Laboratory of Molecular Immunology, National Heart, Lung, and Blood Institute, Bethesda, MD 20892, USA.
J Immunol. 2004 Nov 1;173(9):5361-71. doi: 10.4049/jimmunol.173.9.5361.
IL-21 is a type I cytokine whose receptor is expressed on T, B, and NK cells. Within the B cell lineage, IL-21 regulates IgG1 production and cooperates with IL-4 for the production of multiple Ab classes in vivo. Using IL-21-transgenic mice and hydrodynamics-based gene delivery of IL-21 plasmid DNA into wild-type mice as well as in vitro studies, we demonstrate that although IL-21 induces death of resting B cells, it promotes differentiation of B cells into postswitch and plasma cells. Thus, IL-21 differentially influences B cell fate depending on the signaling context, explaining how IL-21 can be proapoptotic for B cells in vitro yet critical for Ag-specific Ig production in vivo. Moreover, we demonstrate that IL-21 unexpectedly induces expression of both Blimp-1 and Bcl-6, indicating mechanisms as to how IL-21 can serve as a complex regulator of B cell maturation and terminal differentiation. Finally, BXSB-Yaa mice, which develop a systemic lupus erythematosus-like disease, have greatly elevated IL-21, suggesting a role for IL-21 in the development of autoimmune disease.
白细胞介素-21(IL-21)是一种I型细胞因子,其受体在T细胞、B细胞和自然杀伤(NK)细胞上表达。在B细胞谱系中,IL-21调节IgG1的产生,并在体内与IL-4协同作用以产生多种抗体类别。利用IL-21转基因小鼠以及通过基于流体动力学的方法将IL-21质粒DNA导入野生型小鼠,并结合体外研究,我们证明,尽管IL-21诱导静息B细胞死亡,但它促进B细胞分化为转换后B细胞和浆细胞。因此,IL-21根据信号传导背景对B细胞命运产生不同影响,这解释了IL-21在体外对B细胞为何具有促凋亡作用,而在体内对特异性抗原Ig的产生却至关重要。此外,我们证明IL-21意外地诱导了B淋巴细胞诱导成熟蛋白-1(Blimp-1)和B细胞淋巴瘤/白血病-6(Bcl-6)的表达,这表明了IL-21作为B细胞成熟和终末分化复杂调节因子的机制。最后,患有类似系统性红斑狼疮疾病的BXSB-Yaa小鼠体内IL-21水平大幅升高,这表明IL-21在自身免疫性疾病的发展中发挥作用。