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      A germinal center–independent pathway generates unswitched memory B cells early in the primary response

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          Abstract

          Early IgM + and switched Ig + memory B cells develop from a germinal center (GC)–independent pathway, whereas late switched memory cells are GC dependent.

          Abstract

          Memory B cells can be produced from the classical germinal center (GC) pathway or a less understood GC-independent route. We used antigen-based cell enrichment to assess the relative contributions of these pathways to the polyclonal memory B cell pool. We identified a CD38 + GL7 + B cell precursor population that differentiated directly into IgM + or isotype-switched (sw) Ig + memory B cells in a GC-independent fashion in response to strong CD40 stimulation. Alternatively, CD38 + GL7 + B cell precursors had the potential to become Bcl-6 + GC cells that then generated primarily swIg + memory B cells. These results demonstrate that early IgM + and swIg + memory B cells are products of a GC-independent pathway, whereas later switched Ig + memory B cells are products of GC cells.

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          Most cited references19

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          Control of inflammation, cytokine expression, and germinal center formation by BCL-6.

          The gene encoding the BCL-6 transcriptional repressor is frequently translocated and mutated in diffuse large cell lymphoma. Mice with a disrupted BCL-6 gene developed myocarditis and pulmonary vasculitis, had no germinal centers, and had increased expression of T helper cell type 2 cytokines. The BCL-6 DNA recognition motif resembled sites bound by the STAT (signal transducers and activators of transcription) transcription factors, which mediate cytokine signaling. BCL-6 could repress interleukin-4 (IL-4)-induced transcription when bound to a site recognized by the IL-4-responsive transcription factor Stat6. Thus, dysregulation of STAT-responsive genes may underlie the inflammatory disease in BCL-6-deficient mice and participate in lymphoid malignancies.
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            Visualization of specific B and T lymphocyte interactions in the lymph node.

            Early events in the humoral immune response were visualized in lymph nodes by simultaneous tracking of antigen-specific CD4 T and B cells after immunization. The T cells were initially activated in the T cell areas when the B cells were still randomly dispersed in the B cell-rich follicles. Both populations then migrated to the edges of the follicles and interacted there, resulting in CD154-dependent B cell proliferation and germinal center formation. These results provide visual documentation of cognate T-B cell interactions and localize them to the follicular border.
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              Distinct dendritic cell populations sequentially present antigen to CD4 T cells and stimulate different aspects of cell-mediated immunity.

              Peptide:MHC II complexes derived from a fluorescent antigen were detected in vivo to identify the cells that present subcutaneously injected antigen to CD4 T cells. Skin-derived dendritic cells (DCs) that acquired the antigen while in the draining lymph nodes were the first cells to display peptide:MHC II complexes. Presentation by these cells induced CD69, IL-2 production, and maximal proliferation by the T cells. Later, DCs displaying peptide:MHC II complexes migrated from the injection site via a G protein-dependent mechanism. Presentation by these migrants sustained expression of the IL-2 receptor and promoted delayed type hypersensitivity. Therefore, presentation of peptide:MHC II complexes derived from a subcutaneous antigen occurs in two temporally distinct waves with different functional consequences.
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                Author and article information

                Journal
                J Exp Med
                J. Exp. Med
                jem
                The Journal of Experimental Medicine
                The Rockefeller University Press
                0022-1007
                1540-9538
                12 March 2012
                : 209
                : 3
                : 597-606
                Affiliations
                Department of Microbiology, Center for Immunology, University of Minnesota Medical School, Minneapolis, MN 55455
                Author notes
                CORRESPONDENCE Justin J. Taylor: TAYL0611@ 123456umn.edu
                Article
                20111696
                10.1084/jem.20111696
                3302224
                22370719
                6155244b-384a-4be3-a336-014d76461541
                © 2012 Taylor et al.

                This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).

                History
                : 12 August 2011
                : 30 January 2012
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                Medicine
                Medicine

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