4.6 Review

Lipid rafts and B cell signaling

Journal

SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY
Volume 18, Issue 5, Pages 616-626

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.semcdb.2007.07.009

Keywords

B cell; membrane raft; signaling; tyrosine phosphorylation; endocytosis; actin cytoskeleton; ezrin; regulation

Funding

  1. NIAID NIH HHS [R01 AI20038, R01 AI020038] Funding Source: Medline
  2. NIDDK NIH HHS [K01 DK068292-04, K01 DK068292] Funding Source: Medline

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B cells comprise an essential component of the humoral immune system. They are equipped with the unique ability to synthesize and secrete pathogen-neutralizing antibodies, and share with professional antigen presenting cells the ability to internalize foreign antigens, and process them for presentation to helper T cells. Recent evidence indicates that specialized cholesterol- and glycosphingolipid-rich microdomains in the plasma membrane commonly referred to as lipid rafts, serve to compartmentalize key signaling molecules during the different stages of B cell activation including B cell antigen receptor (BCR)-initiated signal transduction, endocytosis of BCR-antigen complexes, loading of antigenic peptides onto MHC class II molecules, MHC-II associated antigen presentation to helper T cells, and receipt of helper signals via the CD40 receptor. Here we review the recent literature arguing for a role of lipid rafts in the spatial organization of B cell function. (C) 2007 Elsevier Ltd. All rights reserved.

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