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Front Cell Infect Microbiol. 2013 Feb 12;3:3. doi: 10.3389/fcimb.2013.00003. eCollection 2013.

Recognition of lipid A variants by the TLR4-MD-2 receptor complex.

Author information

1
Department of Microbiology and Immunology, University of British Columbia, Vancouver, BC, Canada.

Abstract

Lipopolysaccharide (LPS) is a component of the outer membrane of almost all Gram-negative bacteria and consists of lipid A, core sugars, and O-antigen. LPS is recognized by Toll-like receptor 4 (TLR4) and MD-2 on host innate immune cells and can signal to activate the transcription factor NFκB, leading to the production of pro-inflammatory cytokines that initiate and shape the adaptive immune response. Most of what is known about how LPS is recognized by the TLR4-MD-2 receptor complex on animal cells has been studied using Escherichia coli lipid A, which is a strong agonist of TLR4 signaling. Recent work from several groups, including our own, has shown that several important pathogenic bacteria can modify their LPS or lipid A molecules in ways that significantly alter TLR4 signaling to NFκB. Thus, it has been hypothesized that expression of lipid A variants is one mechanism by which pathogens modulate or evade the host immune response. Additionally, several key differences in the amino acid sequences of human and mouse TLR4-MD-2 receptors have been shown to alter the ability to recognize these variations in lipid A, suggesting a host-specific effect on the immune response to these pathogens. In this review, we provide an overview of lipid A variants from several human pathogens, how the basic structure of lipid A is recognized by mouse and human TLR4-MD-2 receptor complexes, as well as how alteration of this pattern affects its recognition by TLR4 and impacts the downstream immune response.

KEYWORDS:

LPS; TLR4; innate immunity; lipid A; signaling

PMID:
23408095
PMCID:
PMC3569842
DOI:
10.3389/fcimb.2013.00003
[Indexed for MEDLINE]
Free PMC Article

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