Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractFlow-switching device for comprehensive two-dimensional gas chromatography    Next AbstractGeneralist and Specialist Mite Herbivores Induce Similar Defense Responses in Maize and Barley but Differ in Susceptibility to Benzoxazinoids »

J Biol Chem


Title:Formyl peptide receptors from immune and vomeronasal system exhibit distinct agonist properties
Author(s):Bufe B; Schumann T; Zufall F;
Address:"Department of Physiology, University of Saarland School of Medicine, 66421 Homburg, Germany. bernd.bufe@uks.eu"
Journal Title:J Biol Chem
Year:2012
Volume:20120802
Issue:40
Page Number:33644 - 33655
DOI: 10.1074/jbc.M112.375774
ISSN/ISBN:1083-351X (Electronic) 0021-9258 (Print) 0021-9258 (Linking)
Abstract:"The formyl peptide receptor (Fpr) family is well known for its contribution to immune defense against pathogens in human and rodent leukocytes. Recently, several structurally related members of these receptors were discovered in sensory neurons of the mouse vomeronasal organ (VNO), key detectors of pheromones and related semiochemicals. Although the biological role of vomeronasal Fprs is not yet clear, the known contribution of other Fprs to host immune defense suggested that they could contribute to vomeronasal pathogen sensing. Precise knowledge about the agonist properties of mouse Fprs is required to determine their function. We expressed all seven mouse and three human Fprs using an in vitro system and tested their activation with 32 selected compounds by conducting high throughput calcium measurements. We found an intriguing functional conservation between human and mouse immune Fprs that is most likely a consequence of closely similar biological constraints. By contrast, our data suggest a neofunctionalization of the vomeronasal Fprs. We show that the vomeronasal receptor mFpr-rs1 can be activated robustly by W-peptide and structural derivatives but not by other typical ligands of immune Fprs. mFpr-rs1 exhibits a stereo-selective preference for peptides containing d-amino acids. The same peptide motifs are contained in pathogenic microorganisms. Thus, the ligand profile of mFpr-rs1 is consistent with a role in vomeronasal pathogen sensing"
Keywords:"Animals Base Sequence Calcium/chemistry/metabolism DNA Primers/genetics HEK293 Cells Humans Immune System/*physiology Ligands Mice Mice, Inbred C57BL Models, Biological Molecular Sequence Data Peptides/chemistry Pheromones Receptors, Formyl Peptide/*chemi;"
Notes:"MedlineBufe, Bernd Schumann, Timo Zufall, Frank eng Research Support, Non-U.S. Gov't 2012/08/04 J Biol Chem. 2012 Sep 28; 287(40):33644-55. doi: 10.1074/jbc.M112.375774. Epub 2012 Aug 2"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 26-12-2024