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      The Other Function: Class II-Restricted Antigen Presentation by B Cells

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          Abstract

          Mature B lymphocytes (B cells) recognize antigens using their B cell receptor (BCR) and are activated to become antibody-producing cells. In addition, and integral to the development of a high-affinity antibodies, B cells utilize the specialized major histocompatibility complex class II (MHCII) antigen presentation pathway to process BCR-bound and internalized protein antigens and present selected peptides in complex with MHCII to CD4+ T cells. This interaction influences the fate of both types of lymphocytes and shapes immune outcomes. Specific, effective, and optimally timed antigen presentation by B cells requires well-controlled intracellular machinery, often regulated by the combined effects of several molecular events. Here, we delineate and summarize these events in four steps along the antigen presentation pathway: (1) antigen capture and uptake by B cells; (2) intersection of internalized antigen/BCRs complexes with MHCII in peptide-loading compartments; (3) generation and regulation of MHCII/peptide complexes; and (4) exocytic transport for presentation of MHCII/peptide complexes at the surface of B cells. Finally, we discuss modulation of the MHCII presentation pathway across B cell development and maturation to effector cells, with an emphasis on the shaping of the MHCII/peptide repertoire by two key antigen presentation regulators in B cells: HLA-DM and HLA-DO.

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          Germinal centres: role in B-cell physiology and malignancy.

          Over the past several years, studies on normal and malignant B cells have provided new insights into the unique physiology of the germinal centre (GC). In particular, advances in technology have allowed a more precise dissection of the phenotypes of GC B cells and the specific transcriptional programmes that are responsible for this phenotype. Furthermore, substantial progress has been made in the understanding of the mechanism controlling the exit of B cells from the GC and the decision to become a memory B cell or plasma cell. This Review focuses on these recent advances and discusses their implications for the pathogenesis of B-cell lymphomas.
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            B cell antigen receptor signaling 101.

            All cells continually survey their environment and make decisions based on cues encountered. This requires specific receptors that detect such cues, then transduce signals that initiate the appropriate responses. B lymphocytes provide an archetypal model for such 'adaptive' cellular responses, where signals transmitted by the B cell Ag-receptor (BCR) influence not only cellular selection, maturation, and survival, but are imperative in generating the ultimate effector function of B cells, i.e. antibody production. While other extracellular stimuli and their cognate receptor signals can also influence B cell development, BCR-mediated signals and the way in which they are integrated and regulated are paramount in defining the cell's physiological fate.
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              B cells use mechanical energy to discriminate antigen affinities.

              The generation of high-affinity antibodies depends on the ability of B cells to extract antigens from the surfaces of antigen-presenting cells. B cells that express high-affinity B cell receptors (BCRs) acquire more antigen and obtain better T cell help. However, the mechanisms by which B cells extract antigen remain unclear. Using fluid and flexible membrane substrates to mimic antigen-presenting cells, we showed that B cells acquire antigen by dynamic myosin IIa-mediated contractions that pull out and invaginate the presenting membranes. The forces generated by myosin IIa contractions ruptured most individual BCR-antigen bonds and promoted internalization of only high-affinity, multivalent BCR microclusters. Thus, B cell contractility contributes to affinity discrimination by mechanically testing the strength of antigen binding.
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                Author and article information

                Contributors
                Journal
                Front Immunol
                Front Immunol
                Front. Immunol.
                Frontiers in Immunology
                Frontiers Media S.A.
                1664-3224
                23 March 2017
                2017
                : 8
                : 319
                Affiliations
                [1] 1Department of Pediatrics, Stanford University , Stanford, CA, USA
                [2] 2Program in Immunology, Stanford University , Stanford, CA, USA
                [3] 3Stanford University , Stanford, CA, USA
                Author notes

                Edited by: Tim Elliott, University of Southampton, UK

                Reviewed by: Andrea Sant, David H. Smith Center for Vaccine Biology and Immunology, USA; Scheherazade Sadegh-Nasseri, Johns Hopkins University, USA

                *Correspondence: Elizabeth D. Mellins, mellins@ 123456stanford.edu

                These authors have contributed equally and are listed alphabetically.

                Specialty section: This article was submitted to Antigen Presenting Cell Biology, a section of the journal Frontiers in Immunology

                Article
                10.3389/fimmu.2017.00319
                5362600
                28386257
                5abc97be-928c-4e19-8aa2-d898ec80b639
                Copyright © 2017 Adler, Jiang, Bhamidipati, Millican, Macaubas, Hung and Mellins.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 21 December 2016
                : 07 March 2017
                Page count
                Figures: 2, Tables: 1, Equations: 0, References: 168, Pages: 14, Words: 12336
                Funding
                Funded by: National Institutes of Health 10.13039/100000002
                Award ID: AI095813, F32 AI126701
                Categories
                Immunology
                Review

                Immunology
                b cell,mhc class ii,antigen processing,antigen presentation,invariant chain,hla-dm,hla-do,germinal center

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