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Lipopolysaccharides from Legionella and Rhizobium stimulate mouse bone marrow granulocytes via Toll-like receptor 2

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TLDR
Using LPSs from bacteria that do not belong to the Enterobacteriaceae, it is shown that in bone marrow cells (BMCs) the LPS of Rhizobium species Sin-1 and of three strains of Legionella pneumophila require TLR2 rather than TLR4 to elicit the expression of CD14.
Abstract
Lipopolysaccharide (LPS) derived from enterobacteria elicit in several cell types cellular responses that are restricted in the use of Toll-like receptor 4 (TLR4) as the principal signal-transducing molecule. A tendency to consider enterobacterial LPS as a prototypic LPS led some authors to present this mechanism as a paradigm accounting for all LPSs in all cell types. However, the structural diversity of LPS does not allow such a general statement. By using LPSs from bacteria that do not belong to the Enterobacteriaceae, we show that in bone marrow cells (BMCs) the LPS of Rhizobium species Sin-1 and of three strains of Legionella pneumophila require TLR2 rather than TLR4 to elicit the expression of CD14. In addition, exposure of BMCs from TLR4-deficient (C3H/HeJ) mice to the lipid A fragment of the Bordetella pertussis LPS inhibits their activation by the Legionella lipid A. The data show selective action of different LPSs via different TLRs, and suggest that TLR2 can interact with many lipid A structures, leading to either agonistic or specific antagonistic effects.

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Journal ArticleDOI

LPS, TLR4 and infectious disease diversity

TL;DR: The hypothesis that the variability of bacterial ligands such as LPS and their innate immune receptors is an important factor in determining the outcome of infectious disease is examined.
Journal ArticleDOI

Therapeutic Targeting of Toll-Like Receptors for Infectious and Inflammatory Diseases and Cancer

TL;DR: Recent advances in the understanding of signaling pathways activated by TLRs, structural insights into TLRs bound to their ligands and antagonists, and approaches to inhibit TLRs are providing possible means by which to interfere with TLRs clinically.
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TLR2 – promiscuous or specific? A critical re-evaluation of a receptor expressing apparent broad specificity

TL;DR: The data together with those reported by other groups reveal that only lipoproteins/lipopeptides are sensed at physiologically concentrations by TLR2 at picomolar levels, which implies that the activity of all other putative bacterial compounds so far reported asTLR2 agonists was most likely due to contaminating highly active natural lipoproteinins and/or lipopeptide.
Journal ArticleDOI

Lipopolysaccharide: Biosynthetic pathway and structure modification.

TL;DR: The relationship between the structure of lipopolysaccharide and the virulence of bacteria is discussed, and the recent discovery of additional enzymes and gene products that can modify the basic structure in some bacteria, especially pathogens are discussed.
Journal ArticleDOI

Gram-positive and gram-negative bacterial toxins in sepsis: a brief review

Girish Ramachandran
- 01 Jan 2014 - 
TL;DR: Over the past decade, the understanding of toxins has markedly improved, allowing for new therapeutic strategies to be developed, and this review summarizes some of these toxins and their role in sepsis.
References
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Journal ArticleDOI

Defective LPS Signaling in C3H/HeJ and C57BL/10ScCr Mice: Mutations in Tlr4 Gene

TL;DR: The mammalian Tlr4 protein has been adapted primarily to subserve the recognition of LPS and presumably transduces the LPS signal across the plasma membrane.
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CD14, a receptor for complexes of lipopolysaccharide (LPS) and LPS binding protein.

TL;DR: 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.
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Differential roles of TLR2 and TLR4 in recognition of gram-negative and gram-positive bacterial cell wall components.

TL;DR: It is demonstrated that TLR2 and TLR4 recognize different bacterial cell wall components in vivo andTLR2 plays a major role in Gram-positive bacterial recognition.
Journal ArticleDOI

The repertoire for pattern recognition of pathogens by the innate immune system is defined by cooperation between Toll-like receptors

TL;DR: The data suggest that TLRs sample the contents of the phagosome independent of the nature of the contents, and can establish a combinatorial repertoire to discriminate among the large number of pathogen-associated molecular patterns found in nature.
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