Variable responses of formyl peptide receptor haplotypes toward bacterial peptides
Identifieur interne : 000132 ( Ncbi/Checkpoint ); précédent : 000131; suivant : 000133Variable responses of formyl peptide receptor haplotypes toward bacterial peptides
Auteurs : Jeannie M. Gripentrog [États-Unis] ; John S. Mills [États-Unis] ; George J. Saari [États-Unis] ; Heini M. Miettinen [États-Unis]Source :
- Immunogenetics [ 0093-7711 ] ; 2008.
Abstract
The chemoattractant neutrophil formyl peptide receptor (FPR) binds bacterial and mitochondrial
Url:
DOI: 10.1007/s00251-008-0277-3
PubMed: 18253729
PubMed Central: 2435592
Affiliations:
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<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Variable responses of formyl peptide receptor haplotypes toward bacterial peptides</title>
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<author><name sortKey="Mills, John S" sort="Mills, John S" uniqKey="Mills J" first="John S." last="Mills">John S. Mills</name>
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<author><name sortKey="Miettinen, Heini M" sort="Miettinen, Heini M" uniqKey="Miettinen H" first="Heini M." last="Miettinen">Heini M. Miettinen</name>
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<series><title level="j">Immunogenetics</title>
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<front><div type="abstract" xml:lang="en"><p>The chemoattractant neutrophil formyl peptide receptor (FPR) binds bacterial and mitochondrial <italic>N</italic>
-formylated peptides, which allows the neutrophils to find the bacterial source and/or site of tissue damage. Certain inflammatory disorders may be due in part to an impaired innate immune system that does not respond to acute bacterial damage in a timely fashion. Because the human FPR is encoded by a large number of different haplotypes arising from ten single-nucleotide polymorphisms, we examined the possibility that some of these haplotypes are functionally distinct. We analyzed the response of three common FPR haplotypes to peptides from <italic>Escherichia coli</italic>
, <italic>Mycobacterium avium</italic>
ssp. <italic>paratuberculosis</italic>
, and human mitochondria. All three haplotypes responded similarly to the <italic>E</italic>
. <italic>coli</italic>
and mitochondrial peptides, whereas one required a higher concentration of the <italic>M</italic>
. <italic>avium</italic>
peptide fMFEDAVAWF for receptor downregulation, receptor signaling, and chemotaxis. This raises the possibility of additional bacterial species differences in functional responses among FPR variants and establishes a precedent with potentially important implications for our innate immune response against bacterial infections. We also investigated whether certain FPR haplotypes are associated with rheumatoid arthritis (RA) by sequencing <italic>FPR1</italic>
from 148 Caucasian individuals. The results suggested that FPR haplotypes do not significantly contribute toward RA.</p>
</div>
</front>
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