Follicular shuttling of marginal zone B cells facilitates antigen transport

被引:401
作者
Cinamon, Guy [1 ,2 ]
Zachariah, Marcus A. [1 ,2 ]
Lam, Olivia M. [1 ,2 ]
Foss, Frank W., Jr. [3 ]
Cyster, Jason G. [1 ,2 ]
机构
[1] Univ Calif San Francisco, Howard Hughes Med Inst, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94143 USA
[3] Univ Virginia, Dept Chem, Charlottesville, VA 22094 USA
关键词
D O I
10.1038/ni1542
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The splenic marginal zone is a site of blood flow, and the specialized B cell population that inhabits this compartment has been linked to the capture and follicular delivery of blood-borne antigens. However, the mechanism of this antigen transport has remained unknown. Here we show that marginal zone B cells were not confined to the marginal zone but continuously shuttled between the marginal zone and follicular areas, such that many of the cells visited a follicle every few hours. Migration to the follicle required the chemokine receptor CXCR5, whereas return to the marginal zone was promoted by the sphingosine 1-phosphate receptors S1P(1) and S1P(3). Treatment with an SIP, antagonist caused displacement of marginal zone B cells from the marginal zone. Marginal zone-follicle shuttling of marginal zone B cells provides an efficient mechanism for systemic antigen capture and delivery to follicular dendritic cells.
引用
收藏
页码:54 / 62
页数:9
相关论文
共 49 条
[1]   Imaging of germinal center selection events during affinity maturation [J].
Allen, Christopher D. C. ;
Okada, Takaharu ;
Tang, H. Lucy ;
Cyster, Jason G. .
SCIENCE, 2007, 315 (5811) :528-531
[2]   Expression of the sphingosine 1-phosphate receptor, S1P1, on T-cells controls thymic emigration [J].
Allende, ML ;
Dreier, JL ;
Mandala, S ;
Proia, RL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (15) :15396-15401
[3]   A chemokine-driven positive feedback loop organizes lymphoid follicles [J].
Ansel, KM ;
Ngo, VN ;
Hyman, PL ;
Luther, SA ;
Förster, R ;
Sedgwick, JD ;
Browning, JL ;
Lipp, M ;
Cyster, JG .
NATURE, 2000, 406 (6793) :309-314
[4]   CXCL13 is required for B1 cell homing, natural antibody production, and body cavity immunity [J].
Ansel, KM ;
Harris, RBS ;
Cyster, JG .
IMMUNITY, 2002, 16 (01) :67-76
[5]  
BROWN JC, 1973, IMMUNOLOGY, V24, P955
[6]   Sphingosine 1-phosphate receptor 1 promotes B cell localization in the splenic marginal zone [J].
Cinamon, G ;
Matloubian, M ;
Lesneski, MJ ;
Xu, Y ;
Low, C ;
Lu, T ;
Proia, RL ;
Cyster, JG .
NATURE IMMUNOLOGY, 2004, 5 (07) :713-720
[7]   Chemokines, sphingosine-1-phosphate, and cell migration in secondary lymphoid organs [J].
Cyster, JG .
ANNUAL REVIEW OF IMMUNOLOGY, 2005, 23 :127-159
[8]   Marginal zone B cells transport and deposit IgM-containing immune complexes onto follicular dendritic cells [J].
Ferguson, AR ;
Youd, ME ;
Corley, RB .
INTERNATIONAL IMMUNOLOGY, 2004, 16 (10) :1411-1422
[9]   A putative chemokine receptor, BLR1, directs B cell migration to defined lymphoid organs and specific anatomic compartments of the spleen [J].
Forster, R ;
Mattis, AE ;
Kremmer, E ;
Wolf, E ;
Brem, G ;
Lipp, M .
CELL, 1996, 87 (06) :1037-1047
[10]   Synthesis and biological evaluation of γ-aminophosphonates as potent, subtype-selective sphingosine 1-phosphate receptor agonists and antagonists [J].
Foss, Frank W., Jr. ;
Snyder, Ashley H. ;
Davis, Michael D. ;
Rouse, Michael ;
Okusa, Mark D. ;
Lynch, Kevin R. ;
Macdonald, Timothy L. .
BIOORGANIC & MEDICINAL CHEMISTRY, 2007, 15 (02) :663-677