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A remarkable spectrum of novel immunoreceptors sharing related immunoglobulin-like domains and signaling potential has been identified in recent years. These receptors have attracted widespread interest because they resemble the TCR, BCR, and FcR complexes in their ability to serve as activating or inhibitory receptors on the cells that bear them. Moreover, they are well positioned to affect both innate and adaptive immunity. The full range of ligands for these new receptor families is still not known, and understanding of their physiological roles is far from complete. This volume is the first attempt to summarize and highlight all known aspects of immunoglobulin-like receptors, providing a topical overview of the roles and characteristic features of the immunoglobulin-like receptors and related molecules in the immune system. Researchers in immunology, molecular biology, cell biology, clinical medicine, and pharmacology will find this book invaluable.
Table des matières
Fc receptors: Activation-inhibition receptor pairing.- Phylogeny of Paired Ig-like Receptors.- Genomic organization of the ILT11 gene, a novel member of the Leukocyte Receptor Cluster (LRC).- Regulated expression of non-polymorphic gp49 molecules on mouse natural killer cells.- Regulation of human Fc?R gene expression.- Molecular recognition by Ig-like receptors, KIRs and Fc?Rs.- Ig modules as discrete structural units to exploit functional and structural aspects of Ig-like receptors.- Structural studies on the leukocyte co-stimulatory molecule, B7-1.- ITIM-bearing receptors in platelets.- Identification of Fc?/u receptor expressed on B lymphocytes and macrophages.- Functional characterization of mouse CD94 by using a novel monoclonal antibody.- Interaction of human cytomegalovirus glycoproteins with immunoreceptors.- Function of gp49A in mast cell activation.- The Fc receptor family structure based strategies for the development of anti-inflammatory drugs.- The mouse gp49 family.- Regulation of B-cell antigen receptor signaling by CD72.- A role for the SH2-containing inositol phosphatase in the biology of natural killer cells and stem cells.- SHIP 1-mediated negative regulation of cell activation and proliferation by Fc?RIIB.- The preBCR signaling through Igß regulates locus accessibility for ordered immunoglobulin gene rearrangements.- Regulation of phospolipase C-?2 and phosphoinositide 3-kinase by adaptor proteins in B cells.- Fc receptor signaling during phagocytosis.- Molecular mechanism of paired immunoglobulin-like receptor B (PIR-B)-mediated inhibitory signal.- IgE stabilizes its high affinity receptor (Fc?RI) on mast cells in vitro and ex vivo: The mechanism of IgE-mediated Fc?RI up-regulation and its physiological meaning.- Autoimmune arthritis andGoodpasture's syndrome induced in Fe? receptor-deficient mice.- Receptors involved in human NK cell activation in the process of natural cytotoxicity.- The regulation of PD-1/PD-L1 pathway and autoimmune diseases.- Identification of the functional recognition site on MHC class I for a NK cell lectin-like receptor.- Characterization of Tml cells, a NKR+ subset of memory-phenotype CD8+ T cells.- How do killer cell Ig-like receptors inhibit natural killer cells?.
Résumé
A remarkable spectrum of novel immunoreceptors sharing related immunoglobulin-like domains and signaling potential has been identified in recent years. These receptors have attracted widespread interest because they resemble the TCR, BCR, and FcR complexes in their ability to serve as activating or inhibitory receptors on the cells that bear them. Moreover, they are well positioned to affect both innate and adaptive immunity. The full range of ligands for these new receptor families is still not known, and understanding of their physiological roles is far from complete. This volume is the first attempt to summarize and highlight all known aspects of immunoglobulin-like receptors, providing a topical overview of the roles and characteristic features of the immunoglobulin-like receptors and related molecules in the immune system. Researchers in immunology, molecular biology, cell biology, clinical medicine, and pharmacology will find this book invaluable.
