Stromal cell networks regulate lymphocyte entry, migration, and territoriality in lymph nodes

被引:749
作者
Bajenoff, Marc
Egen, Jackson G.
Koo, Lily Y.
Laugier, Jean Pierre
Brau, Frederic
Glaichenhaus, Nicolas
Germain, Ronald N. [1 ]
机构
[1] NIAID, Lymphocyte Biol Sect, Immunol Lab, NIH, Bethesda, MD 20892 USA
[2] Univ Nice, INSERM, F-06560 Valbonne, France
[3] Univ Nice, Ctr Commun Microscopie Appl, F-06103 Nice, France
[4] Univ Nice, CNRS, UMR 6097, F-06560 Valbonne, France
关键词
D O I
10.1016/j.immuni.2006.10.011
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
After entry into lymph nodes (LNs), B cells migrate to follicles, whereas T cells remain in the paracortex, with each lymphocyte type showing apparently random migration within these distinct areas. Other than chemokines, the factors contributing to this spatial segregation and to the observed patterns of lymphocyte movement are poorly characterized. By combining confocal, electron, and intravital microscopy, we showed that the fibroblastic reticular cell network regulated naive T cell access to the paracortex and also supported and defined the limits of T cell movement within this domain, whereas a distinct follicular dendritic cell network similarly served as the substratum for movement of follicular B cells. These results highlight the central role of stromal microanatomy in orchestrating cell migration within the LN.
引用
收藏
页码:989 / 1001
页数:13
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