Antigen-engaged B cells undergo chemotaxis toward the T zone and form motile conjugates with helper T cells |
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Authors: | Okada Takaharu Miller Mark J Parker Ian Krummel Matthew F Neighbors Margaret Hartley Suzanne B O'Garra Anne Cahalan Michael D Cyster Jason G |
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Affiliation: | 1Howard Hughes Medical Institute and Department of Microbiology and Immunology, University of CaliforniaSan Francisco, CaliforniaUnited States of America;2Department of Physiology and Biophysics, University of CaliforniaIrvine, CaliforniaUnited States of America;3Department of Neurobiology and Behavior, University of CaliforniaIrvine, CaliforniaUnited States of America;4Department of Pathology, University of CaliforniaSan Francisco, CaliforniaUnited States of America;5Department of Immunobiology, DNAX Research InstitutePalo Alto, CaliforniaUnited States of America;University of MinnesotaUnited States of America |
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Abstract: | 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 μm/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. |
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