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      Mannose-binding lectin enhances Toll-like receptors 2 and 6 signaling from the phagosome

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          Abstract

          Innate immunity is the first-line defense against pathogens and relies on phagocytes, soluble components, and cell-surface and cytosolic pattern recognition receptors. Despite using hard-wired receptors and signaling pathways, the innate immune response demonstrates surprising specificity to different pathogens. We determined how combinatorial use of innate immune defense mechanisms defines the response. We describe a novel cooperation between a soluble component of the innate immune system, the mannose-binding lectin, and Toll-like receptor 2 that both specifies and amplifies the host response to Staphylococcus aureus. Furthermore, we demonstrate that this cooperation occurs within the phagosome, emphasizing the importance of engulfment in providing the appropriate cellular environment to facilitate the synergy between these defense pathways.

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          Most cited references46

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          MD-2, a Molecule that Confers Lipopolysaccharide Responsiveness on Toll-like Receptor 4

          Toll-like receptor 4 (TLR4) is a mammalian homologue of Drosophila Toll, a leucine-rich repeat molecule that can trigger innate responses against pathogens. The TLR4 gene has recently been shown to be mutated in C3H/HeJ and C57BL/10ScCr mice, both of which are low responders to lipopolysaccharide (LPS). TLR4 may be a long-sought receptor for LPS. However, transfection of TLR4 does not confer LPS responsiveness on a recipient cell line, suggesting a requirement for an additional molecule. Here, we report that a novel molecule, MD-2, is requisite for LPS signaling of TLR4. MD-2 is physically associated with TLR4 on the cell surface and confers responsiveness to LPS. MD-2 is thus a link between TLR4 and LPS signaling. Identification of this new receptor complex has potential implications for understanding host defense, as well as pathophysiologic, mechanisms.
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            Phylogenetic perspectives in innate immunity.

            The concept of innate immunity refers to the first-line host defense that serves to limit infection in the early hours after exposure to microorganisms. Recent data have highlighted similarities between pathogen recognition, signaling pathways, and effector mechanisms of innate immunity in Drosophila and mammals, pointing to a common ancestry of these defenses. In addition to its role in the early phase of defense, innate immunity in mammals appears to play a key role in stimulating the subsequent, clonal response of adaptive immunity.
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              CD14, a receptor for complexes of lipopolysaccharide (LPS) and LPS binding protein.

              Leukocytes respond to lipopolysaccharide (LPS) at nanogram per milliliter concentrations with secretion of cytokines such as tumor necrosis factor-alpha (TNF-alpha). Excess secretion of TNF-alpha causes endotoxic shock, an often fatal complication of infection. LPS in the bloodstream rapidly binds to the serum protein, lipopolysaccharide binding protein (LBP), and cellular responses to physiological levels of LPS are dependent on LBP. CD14, a differentiation antigen of monocytes, was found to bind complexes of LPS and LBP, and blockade of CD14 with monoclonal antibodies prevented synthesis of TNF-alpha by whole blood incubated with LPS. Thus, LPS may induce responses by interacting with a soluble binding protein in serum that then binds the cell surface protein CD14.
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                Author and article information

                Journal
                J Exp Med
                The Journal of Experimental Medicine
                The Rockefeller University Press
                0022-1007
                1540-9538
                21 January 2008
                : 205
                : 1
                : 169-181
                Affiliations
                [1 ]Laboratory of Developmental Immunology, Department of Pediatrics and [2 ]Lipid Metabolism Unit, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114
                [3 ]Center for Inflammation Research, University of Edinburgh, Edinburgh EH8 9AG, Scotland, UK
                Author notes

                CORRESPONDENCE W.K. Eddie Ip: eddie_ip@ 123456hms.harvard.edu OR Lynda M. Stuart lstuart@ 123456partners.org

                Article
                20071164
                10.1084/jem.20071164
                2234382
                18180310
                5639985b-ad41-40f9-b007-43a0b8fb3c6c
                Copyright © 2008, The Rockefeller University Press
                History
                : 7 June 2007
                : 29 November 2007
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                Medicine
                Medicine

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