Cellular niches controlling B lymphocyte behavior within bone marrow during development

被引:605
作者
Tokoyoda, K
Egawa, T
Sugiyama, T
Choi, BI
Nagasawa, T
机构
[1] Kyoto Univ, Inst Frontier Med Sci, Dept Med Syst Control, Sakyo Ku, Kyoto 6068507, Japan
[2] Osaka Med Ctr Maternal & Child Hlth, Res Inst, Dept Immunol, Izumi, Osaka 5941101, Japan
[3] Univ Tokyo, Inst Med Sci, Ctr Med Expt, Minato Ku, Tokyo 1088639, Japan
关键词
D O I
10.1016/j.immuni.2004.05.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In bone marrow, hematopoiesis is thought to depend on special microenvironments known as niches that maintain blood cells. However, the identity of niches and interaction of blood cells with niches remain poorly understood. Here we identify stage-specific cellular niches for B lymphopoiesis. The earliest precursors, pre-pro-B cells and end-stage B cells, plasma cells require CXC chemokine ligand (CXCL)12. CXCL12-expressing cells are a small population of stromal cells, scattered throughout bone marrow and located some distance from the cells expressing interleukin (IL)-7. Multipotent hematopoietic progenitors are attached to the processes of CXCL12-expressing cells and pre-pro-B cells adjoin their cell bodies. Maturer pro-B cells that require IL-7 have moved away and adjoin the IL-7-expressing cells. Plasma cells again seed CXCL12-expressing cells. We demonstrate the B lymphocyte characteristic location and movement between specific niches within bone marrow during development and suggest that CXCL12 maintains the cells in the niche.
引用
收藏
页码:707 / 718
页数:12
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