Pillai Shiv, Cariappa Annaiah
Cancer Center, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts 02129, USA.
Nat Rev Immunol. 2009 Nov;9(11):767-77. doi: 10.1038/nri2656.
Bone marrow-derived B cells make an important cell fate choice to develop into either follicular B cells or marginal zone B cells in the spleen, which depends on signalling through the B cell receptor, Notch2, the receptor for B cell-activating factor and the canonical nuclear factor-kappaB pathway, as well as signals involved in the migration and anatomical retention of marginal zone B cells. Recent information discussed in this Review reconciles some of the controversies regarding the role of the B cell receptor in this cell fate decision and a clearer picture has also emerged regarding the anatomical location of ligands for Notch2 in the spleen. This cell fate decision could provide mechanistic insights that are relevant to other commitment events in lymphocytes.
源自骨髓的B细胞会做出重要的细胞命运选择,在脾脏中发育为滤泡B细胞或边缘区B细胞,这取决于通过B细胞受体、Notch2、B细胞激活因子受体和经典核因子-κB途径的信号传导,以及与边缘区B细胞迁移和解剖学定位相关的信号。本综述中讨论的最新信息调和了一些关于B细胞受体在这一细胞命运决定中作用的争议,并且关于脾脏中Notch2配体的解剖位置也出现了更清晰的图景。这一细胞命运决定可以为与淋巴细胞中其他分化事件相关的机制提供见解。