Pike Kelly A, Ratcliffe Michael J H
Department of Immunology, University of Toronto, 1 King's College Circle, Toronto, Ontario, Canada.
Immunol Res. 2006;35(1-2):103-16. doi: 10.1385/IR:35:1:103.
Surface immunoglobulin (sIg) expression has been conserved as a critical checkpoint in B lymphocyte development. In the chicken embryo, only sIg+ B cells are selectively expanded in the bursa of Fabricius, a primary lymphoid organ unique to the avian species. We have previously demonstrated that an interaction between the antigen- binding sites of sIg and a specific bursal ligand(s) is not required to regulate this developmental checkpoint. Rather, the requirement for sIg expression can be attributed to the surface expression of the Igalpha/beta heterodimer associated with sIg. More specifically, ligand-independent signaling downstream of the Igalpha cytoplasmic domain drives all bursal stages of B cell development during embryogenesis. We discuss here a site-directed mutagenesis approach to identify the critical membrane proximal events involved in ligand-independent signaling during B cell development.
表面免疫球蛋白(sIg)的表达作为B淋巴细胞发育中的一个关键检查点一直得以保留。在鸡胚中,只有sIg⁺ B细胞在法氏囊中选择性扩增,法氏囊是鸟类特有的初级淋巴器官。我们之前已经证明,调节这个发育检查点并不需要sIg的抗原结合位点与特定的法氏囊配体之间的相互作用。相反,对sIg表达的需求可归因于与sIg相关的Igalpha / beta异二聚体的表面表达。更具体地说,Igalpha胞质结构域下游的非配体依赖性信号传导驱动胚胎发生过程中B细胞发育的所有法氏囊阶段。我们在此讨论一种定点诱变方法,以确定B细胞发育过程中参与非配体依赖性信号传导的关键膜近端事件。