The recirculating B cell pool contains two functionally distinct, long-lived, posttransitional, follicular B cell Populations

被引:60
作者
Cariappa, Annaiah [1 ]
Boboila, Cristian [1 ]
Moran, Stewart T. [1 ]
Liu, Haoyuan [1 ]
Shi, Hai Ning [1 ]
Pillai, Shiv [1 ]
机构
[1] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Ctr Canc, Charlestown, MA 02129 USA
关键词
D O I
10.4049/jimmunol.179.4.2270
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Disparate models for the development of peripheral B cells may reflect significant heterogeneity in recirculating long-lived B cells that have not been previously accounted for. We show in this study that the murine recirculating B cell pool contains two distinct, long-lived, posttransitional, follicular B cell populations. Follicular Type I IgM(low) B cells require Ag-derived and Btk-dependent signals for their development and make up the majority of cells in the recirculating follicular B cell pool. Follicular type II B cells do not require Btk- or Notch-2-derived signals, make up about a third of the long-lived recirculating B cell pool, and can develop in the absence of Ag. These two follicular populations exhibit differences in basal tyrosine phosphorylation and in BCR-induced proliferation, suggesting that they may represent functionally distinct populations of long-lived recirculating B cells.
引用
收藏
页码:2270 / 2281
页数:12
相关论文
共 58 条
[1]   Plasmodium chabaudi chabaudi infection in mice induces strong B cell responses and striking but temporary changes in splenic cell distribution [J].
Achtman, AH ;
Khan, M ;
MacLennan, ICM ;
Langhorne, J .
JOURNAL OF IMMUNOLOGY, 2003, 171 (01) :317-324
[2]   Transfer of small resting B cells into immunodeficient hosts results in the selection of a self-renewing activated B cell population [J].
Agenès, F ;
Freitas, AA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 189 (02) :319-329
[3]   Resolution of three nonproliferative immature splenic B cell subsets reveals multiple selection points during peripheral B cell maturation [J].
Allman, D ;
Lindsley, RC ;
DeMuth, W ;
Rudd, K ;
Shinton, SA ;
Hardy, RR .
JOURNAL OF IMMUNOLOGY, 2001, 167 (12) :6834-6840
[4]  
ALLMAN DM, 1992, J IMMUNOL, V149, P2533
[5]  
ALLMAN DM, 1993, J IMMUNOL, V151, P4431
[6]   The Yaa mutation promoting murine lupus causes defective development of marginal zone B cells [J].
Amano, H ;
Amano, E ;
Moll, T ;
Marinkovic, D ;
Ibnou-Zekri, N ;
Martinez-Soría, E ;
Semac, I ;
Wirth, T ;
Nitschke, L ;
Izui, S .
JOURNAL OF IMMUNOLOGY, 2003, 170 (05) :2293-2301
[7]  
Amano M, 1998, J IMMUNOL, V161, P1710
[8]   Marginal zone, but not follicular B cells, are potent activators of naive CD4 T cells [J].
Attanavanich, K ;
Kearney, JF .
JOURNAL OF IMMUNOLOGY, 2004, 172 (02) :803-811
[9]   Naive B lymphocytes undergo homeostatic proliferation in response to B cell deficit [J].
Cabatingan, MS ;
Schmidt, MR ;
Sen, R ;
Woodland, RT .
JOURNAL OF IMMUNOLOGY, 2002, 169 (12) :6795-6805
[10]   Nuclear factor κB is required for the development of marginal zone B lymphocytes [J].
Cariappa, A ;
Liou, HC ;
Horwitz, BH ;
Pillai, S .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (08) :1175-1182