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pubmed-article:20620943pubmed:abstractTextMemory B cells express high-affinity, immunoglobulin GB cell receptors (IgG BCRs) that enhance B cell responses, giving rise to the rapid production of high-affinity, IgG antibodies. Despite the central role of IgG BCRs in memory responses, the mechanisms by which the IgG BCRs function to enhance B cell responses are not fully understood. Using high-resolution live-cell imaging, we showed that IgG1 BCRs dramatically enhanced the earliest BCR-intrinsic events that followed within seconds of B cells' encounter with membrane bound antigen, including BCR oligomerization and BCR microcluster growth, leading to Syk kinase recruitment and calcium responses. The enhancement of these early events was dependent on a membrane proximal region of the IgG1 cytoplasmic tail not previously appreciated to play a role in IgG1 BCR signaling. Thus, intrinsic properties of the IgG1 BCR enhance early antigen-driven events that ultimately translate into heightened signaling.lld:pubmed
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pubmed-article:20620943pubmed:authorpubmed-author:SohnHae WonHWlld:pubmed
pubmed-article:20620943pubmed:authorpubmed-author:TolarPavelPlld:pubmed
pubmed-article:20620943pubmed:copyrightInfoCopyright 2010 Elsevier Inc. All rights reserved.lld:pubmed
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pubmed-article:20620943pubmed:dateRevised2011-11-2lld:pubmed
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pubmed-article:20620943pubmed:articleTitleIntrinsic properties of immunoglobulin IgG1 isotype-switched B cell receptors promote microclustering and the initiation of signaling.lld:pubmed
pubmed-article:20620943pubmed:affiliationLaboratory of Immunogenetics, National Institute of Allergy and Infectious Diseases, NIH, Rockville, MD 20852, USA.lld:pubmed
pubmed-article:20620943pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:20620943pubmed:publicationTypeResearch Support, N.I.H., Intramurallld:pubmed
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