Qin X F, Schwers S, Yu W, Papavasiliou F, Suh H, Nussenzweig A, Rajewsky K, Nussenzweig M C
Laboratory of Molecular Immunology, The Rockefeller University, New York, New York 10021, USA.
Nature. 1999 Jan 28;397(6717):355-9. doi: 10.1038/16933.
B-1 B cells are a self-renewing population of B cells that differ from conventional B cells (B-2 cells) in that they are particularly predisposed to auto-antibody production. Although much is known about the signalling pathways that control B-1-cell growth and development, less is known about why these cells are prone to produce autoreactive antibodies. Here we show that B-1 cells, like germinal-centre B cells, can express recombinase-activating genes 1 and 2 (RAG1 and RAG2) and undergo secondary V(D)J recombination of immunoglobulin genes. In addition, B cells from autoimmune-prone NZB mice show high levels of RAG messenger RNA and recombination. We propose that secondary immunoglobulin-gene rearrangements outside organized lymphoid organs may contribute to the development of autoreactive antibodies.
B-1 B细胞是一类自我更新的B细胞群体,与传统B细胞(B-2细胞)不同,它们特别倾向于产生自身抗体。尽管人们对控制B-1细胞生长和发育的信号通路了解很多,但对于这些细胞为何易于产生自身反应性抗体却知之甚少。我们在此表明,B-1细胞与生发中心B细胞一样,能够表达重组激活基因1和2(RAG1和RAG2),并经历免疫球蛋白基因的二次V(D)J重组。此外,易患自身免疫性疾病的NZB小鼠的B细胞显示出高水平的RAG信使核糖核酸和重组。我们提出,有组织的淋巴器官外的二次免疫球蛋白基因重排可能有助于自身反应性抗体的产生。