Development and Migration of Plasma Cells in the Mouse Lymph Node

被引:104
作者
Fooksman, David R. [1 ,2 ]
Schwickert, Tanja A.
Victora, Gabriel D.
Dustin, Michael L. [1 ,2 ]
Nussenzweig, Michel C. [3 ]
Skokos, Dimitris [4 ]
机构
[1] NYU, Sch Med, Program Mol Pathogenesis, New York, NY 10016 USA
[2] NYU, Sch Med, Dept Pathol, Skirball Inst Biomol Med, New York, NY 10016 USA
[3] Rockefeller Univ, Lab Mol Immunol, Howard Hughes Med Inst, New York, NY 10021 USA
[4] Regeneron Pharmaceut Inc, Tarrytown, NY 10591 USA
基金
美国国家卫生研究院;
关键词
IN-VIVO; AFFINITY MATURATION; BLIMP-1; EXPRESSION; ANTIBODY-RESPONSES; IMMUNE-RESPONSE; B-LYMPHOCYTES; BONE-MARROW; RESPONSIVENESS; MICROENVIRONMENTS; DIFFERENTIATION;
D O I
10.1016/j.immuni.2010.06.015
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
In this study, we imaged the differentiation and migratory behavior of nascent plasma cells (PCs) in mouse lymph nodes by intravital microscopy. Pre-PCs exhibited a unique migration pattern characterized by long, linear paths that were randomly oriented. Although chemotaxis via G alpha i coupled-receptors has been implicated in PC migration, treatment with Pertussis toxin (Ptx), which ablates these signals, did not prevent movement of pre-PCs while it arrested other lymphocytes. In vitro, pre-PCs displayed processive amoeboid locomotion on surfaces coated with integrin ligand, whereas fully differentiated PCs moved slowly or were arrested. Both PC arrest and differentiation occurred in the medullary cords. Ptx treatment before PC differentiation blocked their accumulation in the medullary cords but pre-PCs still differentiated in other lymph node regions. Taken together, we suggest pre-PCs undergo a persistent random walk to find the medullary cords, where localized chemokines help retain these cells until they undergo differentiation and arrest in situ.
引用
收藏
页码:118 / 127
页数:10
相关论文
共 40 条
[1]
Germinal center dark and light zone organization is mediated by CXCR4 and CXCR5 [J].
Allen, CDC ;
Ansel, KM ;
Low, C ;
Lesley, R ;
Tamamura, H ;
Fujii, N ;
Cyster, JG .
NATURE IMMUNOLOGY, 2004, 5 (09) :943-952
[2]
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
[3]
Commitment of B lymphocytes to a plasma cell fate is associated with Blimp-1 expression in vivo [J].
Angelin-Duclos, C ;
Cattoretti, G ;
Lin, KI ;
Calame, K .
JOURNAL OF IMMUNOLOGY, 2000, 165 (10) :5462-5471
[4]
Stromal cell networks regulate lymphocyte entry, migration, and territoriality in lymph nodes [J].
Bajenoff, Marc ;
Egen, Jackson G. ;
Koo, Lily Y. ;
Laugier, Jean Pierre ;
Brau, Frederic ;
Glaichenhaus, Nicolas ;
Germain, Ronald N. .
IMMUNITY, 2006, 25 (06) :989-1001
[5]
APRIL is critical for plasmablast survival in the bone marrow and poorly expressed by early-life bone marrow stromal cells [J].
Belnoue, Elodie ;
Pihlgren, Maria ;
McGaha, Tracy L. ;
Tougne, Chantal ;
Rochat, Anne-Francoise ;
Bossen, Claudia ;
Schneider, Pascal ;
Huard, Bertrand ;
Lambert, Paul-Henri ;
Siegrist, Claire-Anne .
BLOOD, 2008, 111 (05) :2755-2764
[6]
Regulatory mechanisms that determine the development and function of plasma cells [J].
Calame, KL ;
Lin, KI ;
Tunyaplin, C .
ANNUAL REVIEW OF IMMUNOLOGY, 2003, 21 :205-230
[7]
Random walk models in biology [J].
Codling, Edward A. ;
Plank, Michael J. ;
Benhamou, Simon .
JOURNAL OF THE ROYAL SOCIETY INTERFACE, 2008, 5 (25) :813-834
[8]
Search along persistent random walks [J].
Friedrich, Benjamin M. .
PHYSICAL BIOLOGY, 2008, 5 (02)
[9]
THE SUBCELLULAR-LOCALIZATION OF IMMUNOGLOBULIN IN MOUSE PLASMA-CELLS, AS STUDIED WITH IMMUNOFERRITIN CYTO-CHEMISTRY ON ULTRATHIN FROZEN-SECTIONS [J].
GEUZE, HJ ;
SLOT, JW .
AMERICAN JOURNAL OF ANATOMY, 1980, 158 (02) :161-169
[10]
A coordinated change in chemokine responsiveness guides plasma cell movements [J].
Hargreaves, DC ;
Hyman, PL ;
Lu, TT ;
Ngo, VN ;
Bidgol, A ;
Suzuki, G ;
Zou, YR ;
Littman, DR ;
Cyster, JG .
JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 194 (01) :45-56