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PLoS Biol.
2005 Jun;3(6):e150. Epub 2005 May 3.
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Antigen-engaged B cells undergo chemotaxis toward the T zone and form motile conjugates with helper T cells.
Okada T
,
Miller MJ
,
Parker I
,
Krummel MF
,
Neighbors M
,
Hartley SB
,
O'Garra A
,
Cahalan MD
,
Cyster JG
.
Howard Hughes Medical Institute, Department of Microbiology and Immunology, University of California, San Francisco, California, USA.
Interactions between B and T cells are essential for most antibody responses, but the dynamics of these interactions are poorly understood. By two-photon microscopy of intact lymph nodes, we show that upon exposure to antigen, B cells migrate with directional preference toward the B-zone-T-zone boundary in a CCR7-dependent manner, through a region that exhibits a CCR7-ligand gradient. Initially the B cells show reduced motility, but after 1 d, motility is increased to approximately 9 microm/min. Antigen-engaged B cells pair with antigen-specific helper T cells for 10 to more than 60 min, whereas non-antigen-specific interactions last less than 10 min. B cell-T cell conjugates are highly dynamic and migrate extensively, being led by B cells. B cells occasionally contact more than one T cell, whereas T cells are strictly monogamous in their interactions. These findings provide evidence of lymphocyte chemotaxis in vivo, and they begin to define the spatiotemporal cellular dynamics associated with T cell-dependent antibody responses.
Publication Types:
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, P.H.S.
PMID: 15857154 [PubMed - indexed for MEDLINE]
PMCID: PMC1088276
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