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
相关论文
共 53 条
[21]
Regulation of marginal zone B cell development by MINT, a suppressor of Notch/RBP-J signaling pathway [J].
Kuroda, K ;
Han, H ;
Tani, S ;
Tanigaki, K ;
Tun, T ;
Furukawa, T ;
Taniguchi, Y ;
Kurooka, H ;
Hamada, Y ;
Toyokuni, S ;
Honjo, T .
IMMUNITY, 2003, 18 (02) :301-312
[22]
Notch ligands delta1 and jagged1 transmit distinct signals to T-cell precursors [J].
Lehar, SM ;
Dooley, J ;
Farr, AG ;
Bevan, MJ .
BLOOD, 2005, 105 (04) :1440-1447
[23]
B cell development in the spleen takes place in discrete steps and is determined by the quality of B cell receptor-derived signals [J].
Loder, F ;
Mutschler, B ;
Ray, RJ ;
Paige, CJ ;
Sideras, P ;
Torres, R ;
Lamers, MC ;
Carsetti, R .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 190 (01) :75-89
[24]
Development and selection of marginal zone B cells [J].
Lopes-Carvalho, T ;
Kearney, JF .
IMMUNOLOGICAL REVIEWS, 2004, 197 :192-205
[25]
Anchoring Notch genetics and biochemistry: Structural analysis of the ankyrin domain sheds light on existing data [J].
Lubman, OY ;
Korolev, SV ;
Kopan, R .
MOLECULAR CELL, 2004, 13 (05) :619-626
[26]
Regulation of lymphoid development, differentiation, and function by the notch pathway [J].
Maillard, I ;
Fang, T ;
Pear, WS .
ANNUAL REVIEW OF IMMUNOLOGY, 2005, 23 :945-974
[27]
Martin D, 2002, BRILLS TIBET STU LIB, V2, P335
[28]
Positive selection from newly formed to marginal zone B cells depends on the rate of clonal production, CD19, and btk [J].
Martin, F ;
Kearney, JF .
IMMUNITY, 2000, 12 (01) :39-49
[29]
McCright B, 2002, DEVELOPMENT, V129, P1075
[30]
Structure and function of the spleen [J].
Mebius, RE ;
Kraal, G .
NATURE REVIEWS IMMUNOLOGY, 2005, 5 (08) :606-616