Shapira S K, Vercelli D, Jabara H H, Fu S M, Geha R S
Division of Immunology, Children's Hospital, Boston, Massachusetts 02115.
J Exp Med. 1992 Jan 1;175(1):289-92. doi: 10.1084/jem.175.1.289.
The molecular events leading to immunoglobulin E (IgE) synthesis in human sIgE- B cells stimulated with interleukin 4 (IL-4) and anti-CD40 monoclonal antibody (mAb) 626.1 were analyzed. Anti-CD40 mAb increased the levels of IL-4-induced germline C epsilon transcripts and induced the production of mature C epsilon mRNA. These effects were dependent on the presence of IL-4. Nested primer PCR revealed deletional switch recombination occurring only in B cell stimulated with both IL-4 and anti-CD40 mAb. DNA sequence analysis of switch fragments showed direct S mu/S epsilon joining, without the deletions or duplications within S mu often found in B cells stimulated with IL-4 and Epstein-Barr virus. Analysis of the switch junction map sites showed "hot spots" for recombination within S mu, but not within S epsilon. These findings indicate that IL-4 provides a signal to B cells to induce germline C epsilon transcription and concurrent CD40 engagement induces S mu/S epsilon deletional switch recombination, production of mature C epsilon mRNA, and IgE synthesis.
分析了在白细胞介素4(IL-4)和抗CD40单克隆抗体(mAb)626.1刺激下人分泌型IgE B细胞中导致免疫球蛋白E(IgE)合成的分子事件。抗CD40 mAb增加了IL-4诱导的胚系Cε转录本水平,并诱导了成熟Cε mRNA的产生。这些效应依赖于IL-4的存在。巢式引物PCR显示缺失型转换重组仅发生在同时用IL-4和抗CD40 mAb刺激的B细胞中。转换片段的DNA序列分析显示直接的Sμ/Sε连接,而没有在用IL-4和爱泼斯坦-巴尔病毒刺激的B细胞中常见的Sμ内的缺失或重复。对转换连接图谱位点的分析显示Sμ内存在重组“热点”,而Sε内没有。这些发现表明,IL-4向B细胞提供信号以诱导胚系Cε转录,同时CD40参与诱导Sμ/Sε缺失型转换重组、成熟Cε mRNA的产生和IgE合成。