Lunatic and Manic Fringe Cooperatively Enhance Marginal Zone B Cell Precursor Competition for Delta-like 1 in Splenic Endothelial Niches

被引:118
作者
Tan, Joanne B. [1 ,2 ]
Xu, Keli [1 ]
Cretegny, Kira [1 ,2 ]
Visan, Ioana [1 ,2 ]
Yuan, Julie S. [1 ,2 ]
Egan, Sean E. [1 ,3 ]
Guidos, Cynthia J. [1 ,2 ]
机构
[1] Hosp Sick Children, Res Inst, Program Dev & Stem Cell Biol, Toronto, ON M5G 1L7, Canada
[2] Univ Toronto, Fac Med, Dept Immunol, Toronto, ON M5S 1A8, Canada
[3] Univ Toronto, Fac Med, Dept Mol Genet, Toronto, ON M5S 1A8, Canada
基金
加拿大健康研究院;
关键词
MICROCIRCULATORY PATHWAYS; NOTCH1; DIFFERENTIATION; SEGMENTATION; RECEPTORS; LIGANDS; DELTA-LIKE-1; REQUIREMENT; LYMPHOCYTES; INHIBITION;
D O I
10.1016/j.immuni.2008.12.016
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Notch2 activation induced by Delta-like-1 (DL1) drives development of splenic marginal zone (MZ) B cells, an innate-like lineage that protects against sepsis. DL1 interacts with Notch2 weakly, but it is not known whether enhancement of DL1-induced Notch2 activation by Fringe glycosyltransferases is important for MZ B cell development. Furthermore, DL1-expressing cells that promote MZ B cell development have not been identified. We show that Lunatic Fringe (Lfng) and Manic Fringe (Mfng) cooperatively enhanced the DL1-Notch2 interaction to promote MZ B cell development. We also identified radio-resistant red pulp endothelial cells in the splenic MZ that express high amounts of DL1 and promoted MZ B generation. Finally, MZ B cell precursor competition for DL1 homeostatically regulated entry into the MZ B cell pool. Our study has revealed that the Fringe-Notch2 interaction has important functions in vivo and provides insights into mechanisms regulating MZ B cell development.
引用
收藏
页码:254 / 263
页数:10
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