Developmental switches in chemokine response profiles during B cell differentiation and maturation

被引:181
作者
Bowman, EP
Campbell, JJ
Soler, D
Dong, ZJ
Manlongat, N
Picarella, D
Hardy, RR
Butcher, EC [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Pathol 5324, Lab Immunol & Vasc Biol, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Med, Ctr Digest Dis, Stanford, CA 94305 USA
[3] Vet Affairs, Palo Alto Hlth Care Syst, Ctr Mol Biol & Med, Palo Alto, CA 94305 USA
[4] Fox Chase Canc Ctr, Inst Canc Res, Philadelphia, PA 19111 USA
关键词
B lymphocyte; chemokines; chemotaxis; bone marrow; hematopoiesis;
D O I
10.1084/jem.191.8.1303
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Developing B cells undergo dramatic changes in their responses to chemoattractant cytokines (chemokines) and in expression of chemokine receptors. Bone marrow pre-pro-B cells (AA4.1(+)/natural killer 1.1(-) Fraction A cells) and cells capable of generating pro-B colonies in the presence of interleukin 7 and flt3 ligand migrate to thymus-expressed chemokine (TECK), a response lost in later stages of B cell development. B cell-attracting chemokine 1 (BCA-1) responses correlate with CXC chemokine receptor (CXCR)5 expression, are first displayed by a pro-B cell subset, are lost in pre-B cells, and then are regained just before and after egress from the marrow. All peripheral B cell subsets, including follicular and germinal center as well as marginal zone and peritoneal B1 B cells, respond to BCA-1, implying that responsiveness to this follicular chemokine is not sufficient to predict follicle localization. Responses to the CC chemokine receptor (CCR)7 ligands secondary lymphoid tissue chemoattractant (SLC) and macrophage inflammatory protein (MIP)-3 beta, implicated in homing to lymphoid tissues, are upregulated before B cell exit from the marrow, but increase further in the periphery and are shared by all peripheral B cells. In contrast, responsiveness to MIP-3 alpha and expression of CCR6 are acquired only after emigration to the periphery and during maturation into the recirculating B cell pool. Chemotaxis to stromal cell-derived factor lot is observed at all stages of B cell differentiation. Thus, unique patterns of chemokine responses may help define developing B cell populations and direct their maturation in the marrow and migration to the periphery.
引用
收藏
页码:1303 / 1317
页数:15
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