Lin Kuo-I, Tunyaplin Chainarong, Calame Kathryn
Departments of Microbiology and Biochemistry and Molecular Biophysics, Columbia University College of Physicians and Surgeons, New York, NY 10032-2704, USA.
Immunol Rev. 2003 Aug;194:19-28. doi: 10.1034/j.1600-065x.2003.00040.x.
Plasma cells are the terminally differentiated effector cells of the B lymphocyte lineage. Recently, studies using genetically altered mice and analyses of global gene expression programs have significantly expanded our understanding of the molecular mechanisms regulating plasmacytic differentiation. Specific molecular components of a multistep cascade of transcriptional regulators have been identified. Furthermore, two transcriptional regulators, X box binding protein-1 (XBP-1) and B lymphocyte induced maturation protein-1 (Blimp-1), have been shown to be necessary for plasmacytic differentiation. In addition to providing a mechanistic basis for the induction of genes necessary for immunoglobulin secretion, cessation of cell cycle and other phenotypic changes characteristic of terminally differentiated plasma cells, these studies have led to the important concept that plasmacytic differentiation involves repression of regulators, such as Bcl-6 and Pax5, that are necessary to maintain the earlier developmental phenotype of activated, germinal center B cells. This review describes our current understanding of the transcriptional cascades regulating terminal differentiation of B cells.
浆细胞是B淋巴细胞谱系的终末分化效应细胞。最近,利用基因工程改造小鼠的研究以及对整体基因表达程序的分析,极大地拓展了我们对调控浆细胞分化分子机制的理解。已确定了转录调节因子多步骤级联反应的特定分子成分。此外,两种转录调节因子,即X盒结合蛋白1(XBP-1)和B淋巴细胞诱导成熟蛋白1(Blimp-1),已被证明是浆细胞分化所必需的。这些研究除了为诱导免疫球蛋白分泌、细胞周期停止及终末分化浆细胞其他特征性表型变化所需的基因提供了机制基础外,还引出了一个重要概念,即浆细胞分化涉及对诸如Bcl-6和Pax5等调节因子的抑制,而这些调节因子对于维持活化生发中心B细胞的早期发育表型是必需的。本综述描述了我们目前对调控B细胞终末分化转录级联反应的理解。