Butch A W, Chung G H, Hoffmann J W, Nahm M H
Department of Pathology, Washington University School of Medicine, St. Louis, MO 63110.
J Immunol. 1993 Jan 1;150(1):39-47.
Germinal centers (GC) primarily consist of B cells along with a small number of T cells (5 to 10%) and follicular dendritic cells (FDC) (< or = 1%). Although extensive Ag-driven B cell proliferation and maturation occurs in GC, very little is known about the role of cytokines in the development of GC B cells. Therefore, to identify cytokines present in the GC microenvironment that may influence B cell development, we systematically examined cytokine gene expression by GC cells. GC T cells (CD57+/CD4+), GC B cells (CD77+), and FDC (HJ2+) were isolated from human tonsils by cell sorting using a flow cytometer. Freshly isolated GC cells were examined for mRNA expression for IL-1 alpha, IL-1 beta, IL-2, IL-3, IL-4, IL-5, IL-6, IL-10, TNF-alpha, and IFN-gamma using reverse transcription polymerase chain reaction. Freshly isolated GC T cells consistently expressed IL-4 mRNA (11 of 12 tonsils), whereas CD57- Th cells (mostly non-GC Th cells) were often negative for IL-4 mRNA. When the other nine cytokine mRNA were studied, freshly isolated CD57+ Th cells occasionally expressed mRNA for IL-10, TNF-alpha, and IFN-gamma. CD57- Th cells were occasionally positive for IL-1 beta, IL-10, IFN-gamma, and TNF-alpha, and negative for IL-2 and IL-6. Freshly isolated GC B cells as well as FDC failed to express detectable quantities of mRNA for all 10 cytokines that were studied. Thus, IL-4 is the only cytokine out of 10 that is consistently expressed in GC and may be important for the development of B cells in GC. After stimulation of CD57+ Th cells with PWM, production of IL-4 mRNA was dramatically reduced, whereas CD57- Th cell production of IL-4 was greatly augmented. This finding indicates that GC T cells may differ from other Th cells in cytokine gene expression and that results of cytokine production obtained after in vitro stimulation do not always reflect in vivo results.
生发中心(GC)主要由B细胞组成,同时还含有少量T细胞(5%至10%)和滤泡树突状细胞(FDC)(≤1%)。尽管在生发中心会发生广泛的抗原驱动的B细胞增殖和成熟,但关于细胞因子在生发中心B细胞发育中的作用却知之甚少。因此,为了确定生发中心微环境中可能影响B细胞发育的细胞因子,我们系统地检测了生发中心细胞的细胞因子基因表达。通过流式细胞仪细胞分选,从人扁桃体中分离出生发中心T细胞(CD57⁺/CD4⁺)、生发中心B细胞(CD77⁺)和FDC(HJ2⁺)。使用逆转录聚合酶链反应检测新鲜分离的生发中心细胞中IL-1α、IL-1β、IL-2、IL-3、IL-4、IL-5、IL-6、IL-10、TNF-α和IFN-γ的mRNA表达。新鲜分离的生发中心T细胞持续表达IL-4 mRNA(12个扁桃体中有11个),而CD57⁻ Th细胞(大多为非生发中心Th细胞)通常IL-4 mRNA呈阴性。当研究其他9种细胞因子mRNA时,新鲜分离的CD57⁺ Th细胞偶尔表达IL-10、TNF-α和IFN-γ的mRNA。CD57⁻ Th细胞偶尔IL-1β、IL-10、IFN-γ和TNF-α呈阳性,而IL-2和IL-6呈阴性。新鲜分离的生发中心B细胞以及FDC未能表达所研究的全部10种细胞因子的可检测量的mRNA。因此,IL-4是所研究的10种细胞因子中唯一在生发中心持续表达的细胞因子,可能对生发中心B细胞的发育很重要。用PWM刺激CD57⁺ Th细胞后,IL-4 mRNA的产生显著减少,而CD57⁻ Th细胞产生的IL-4则大大增加。这一发现表明,生发中心T细胞在细胞因子基因表达上可能与其他Th细胞不同,并且体外刺激后获得的细胞因子产生结果并不总是反映体内结果。