Department of Immunobiology, Yale University, New Haven, CT 06519.
Department of Genetics, Yale University, New Haven, CT 06519.
J Immunol. 2018 Dec 15;201(12):3569-3579. doi: 10.4049/jimmunol.1500497. Epub 2018 Nov 16.
We examined the unique contributions of the cytokines IL-21 and IL-4 on germinal center (GC) B cell initiation and subsequent maturation in a murine model system. Similar to other reports, we found T follicular helper cell expression of IL-21 begins prior to T follicular helper cell migration into the B cell follicle and precedes that of IL-4. Consistent with this timing, IL-21 signaling has a greater influence on the perifollicular pre-GC B cell transition to the intrafollicular stage. Notably, Bcl6 B cells can form in the combined absence of IL-21R- and STAT6-derived signals; however, these nascent GC B cells cease to proliferate and are more prone to apoptosis. When B cells lack either IL-21R or STAT6, aberrant GCs form atypical centroblasts and centrocytes that differ in their phenotypic maturation and costimulatory molecule expression. Thus, IL-4 and IL-21 play nonredundant roles in the phased progression of GC B cell development that can initiate in the combined absence of these cytokine signals.
我们在小鼠模型系统中研究了细胞因子 IL-21 和 IL-4 对生发中心 (GC) B 细胞起始和随后成熟的独特贡献。与其他报道相似,我们发现滤泡辅助性 T 细胞表达的 IL-21 先于滤泡辅助性 T 细胞迁移到 B 细胞滤泡,并早于 IL-4 的表达。与这一时间一致,IL-21 信号对周围生发中心前 B 细胞向滤泡内阶段的过渡有更大的影响。值得注意的是,Bcl6+B 细胞可以在缺乏 IL-21R 和 STAT6 衍生信号的情况下形成;然而,这些新生的 GC B 细胞停止增殖,更容易发生凋亡。当 B 细胞缺乏 IL-21R 或 STAT6 时,异常生发中心形成不同表型成熟和共刺激分子表达的异常中心母细胞和中心细胞。因此,IL-4 和 IL-21 在 GC B 细胞发育的分阶段进展中发挥非冗余作用,在这些细胞因子信号缺失的情况下,GC B 细胞发育可以启动。