The role of Toll-like receptors and Nod proteins in bacterial infection
Our understanding of innate immunity in mammals has greatly expanded following the discovery of the family of membrane-bound receptors, called the Toll-like receptors (TLRs). More recently, the nucleotide-binding oligomerisation domain (Nod) molecules, Nod1 and Nod2, which are cytoplasmic surveillan...
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Published in | Molecular immunology Vol. 41; no. 11; pp. 1099 - 1108 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
England
Elsevier Ltd
01.11.2004
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Subjects | |
Online Access | Get full text |
ISSN | 0161-5890 1872-9142 |
DOI | 10.1016/j.molimm.2004.06.012 |
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Abstract | Our understanding of innate immunity in mammals has greatly expanded following the discovery of the family of membrane-bound receptors, called the Toll-like receptors (TLRs). More recently, the nucleotide-binding oligomerisation domain (Nod) molecules, Nod1 and Nod2, which are cytoplasmic surveillance proteins, have also been shown to be involved in the innate immune response. These two classes of detection molecules, classified as “pattern recognition receptors” (PRRs), detect microbial ligands in order to initiate a defense response to fight infectious disease. These microbial ligands or “pathogen-associated molecular patterns” (PAMPs), detected by TLRs and Nods are often structural components of the microorganism that are not subject to much variation. These include such factors as lipopolysaccharide (LPS) and peptidoglycan from the cell walls of bacteria. In order to understand the role of TLRs and Nod proteins in infectious disease in vivo it is important to define the site of interaction between PRRs and PAMPS. Additionally, the challenge of mice deficient in the various PRRs in natural infection models will help to decipher the contribution of these molecules not only in the innate immune response against pathogen infection but also how these proteins may instruct the adaptive immune response in order to have a tailored immune response against a particular microbe. |
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AbstractList | Our understanding of innate immunity in mammals has greatly expanded following the discovery of the family of membrane-bound receptors, called the Toll-like receptors (TLRs). More recently, the nucleotide-binding oligomerisation domain (Nod) molecules, Nod1 and Nod2, which are cytoplasmic surveillance proteins, have also been shown to be involved in the innate immune response. These two classes of detection molecules, classified as "pattern recognition receptors" (PRRs), detect microbial ligands in order to initiate a defense response to fight infectious disease. These microbial ligands or "pathogen-associated molecular patterns" (PAMPs), detected by TLRs and Nods are often structural components of the microorganism that are not subject to much variation. These include such factors as lipopolysaccharide (LPS) and peptidoglycan from the cell walls of bacteria. In order to understand the role of TLRs and Nod proteins in infectious disease in vivo it is important to define the site of interaction between PRRs and PAMPS. Additionally, the challenge of mice deficient in the various PRRs in natural infection models will help to decipher the contribution of these molecules not only in the innate immune response against pathogen infection but also how these proteins may instruct the adaptive immune response in order to have a tailored immune response against a particular microbe. Our understanding of innate immunity in mammals has greatly expanded following the discovery of the family of membrane-bound receptors, called the Toll-like receptors (TLRs). More recently, the nucleotide-binding oligomerisation domain (Nod) molecules, Nod1 and Nod2, which are cytoplasmic surveillance proteins, have also been shown to be involved in the innate immune response. These two classes of detection molecules, classified as "pattern recognition receptors" (PRRs), detect microbial ligands in order to initiate a defense response to fight infectious disease. These microbial ligands or "pathogen-associated molecular patterns" (PAMPs), detected by TLRs and Nods are often structural components of the microorganism that are not subject to much variation. These include such factors as lipopolysaccharide (LPS) and peptidoglycan from the cell walls of bacteria. In order to understand the role of TLRs and Nod proteins in infectious disease in vivo it is important to define the site of interaction between PRRs and PAMPS. Additionally, the challenge of mice deficient in the various PRRs in natural infection models will help to decipher the contribution of these molecules not only in the innate immune response against pathogen infection but also how these proteins may instruct the adaptive immune response in order to have a tailored immune response against a particular microbe.Our understanding of innate immunity in mammals has greatly expanded following the discovery of the family of membrane-bound receptors, called the Toll-like receptors (TLRs). More recently, the nucleotide-binding oligomerisation domain (Nod) molecules, Nod1 and Nod2, which are cytoplasmic surveillance proteins, have also been shown to be involved in the innate immune response. These two classes of detection molecules, classified as "pattern recognition receptors" (PRRs), detect microbial ligands in order to initiate a defense response to fight infectious disease. These microbial ligands or "pathogen-associated molecular patterns" (PAMPs), detected by TLRs and Nods are often structural components of the microorganism that are not subject to much variation. These include such factors as lipopolysaccharide (LPS) and peptidoglycan from the cell walls of bacteria. In order to understand the role of TLRs and Nod proteins in infectious disease in vivo it is important to define the site of interaction between PRRs and PAMPS. Additionally, the challenge of mice deficient in the various PRRs in natural infection models will help to decipher the contribution of these molecules not only in the innate immune response against pathogen infection but also how these proteins may instruct the adaptive immune response in order to have a tailored immune response against a particular microbe. |
Author | Philpott, Dana J. Girardin, Stephen E. |
Author_xml | – sequence: 1 givenname: Dana J. surname: Philpott fullname: Philpott, Dana J. email: philpott@pasteur.fr organization: Immunité Innée et Signalisation, Institut Pasteur, 28 rue du Dr. Roux, 75724 Paris Cedex 15, France – sequence: 2 givenname: Stephen E. surname: Girardin fullname: Girardin, Stephen E. organization: Pathogénie Microbienne Moléculaire, Institut Pasteur, 28 rue du Dr. Roux, 75724 Paris Cedex 15, France |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/15476921$$D View this record in MEDLINE/PubMed |
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Keywords | Toll-like receptors Innate immunity Nod2 Nod1 Microbial infection |
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SubjectTerms | Adaptor Proteins, Signal Transducing - immunology Adaptor Proteins, Signal Transducing - physiology Animals Bacteria Bacterial Infections - immunology Drosophila Proteins - immunology Drosophila Proteins - physiology Gram-Negative Bacterial Infections - immunology Innate immunity Intracellular Signaling Peptides and Proteins - immunology Intracellular Signaling Peptides and Proteins - physiology Kinesin Membrane Glycoproteins - immunology Membrane Glycoproteins - physiology Mice Microbial infection Microtubule Proteins - immunology Microtubule Proteins - physiology Nod1 Nod1 Signaling Adaptor Protein Nod2 Nod2 Signaling Adaptor Protein Receptors, Cell Surface - immunology Receptors, Cell Surface - physiology Toll-Like Receptors |
Title | The role of Toll-like receptors and Nod proteins in bacterial infection |
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