Document Detail


Cloning, expression, cellular distribution, and role in chemotaxis of a C5a receptor in rainbow trout: the first identification of a C5a receptor in a nonmammalian species.
MedLine Citation:
PMID:  15034053     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
C3a, C4a, and C5a anaphylatoxins generated during complement activation play a key role in inflammation. C5a is the most potent of the three anaphylatoxins in eliciting biological responses. The effects of C5a are mediated by its binding to C5a receptor (C5aR, CD88). To date, C5aR has only been identified and cloned in mammalian species, and its evolutionary history remains ill-defined. To gain insights into the evolution, conserved structural domains, and functions of C5aR, we have cloned and characterized a C5aR in rainbow trout, a teleost fish. The isolated cDNA encoded a 350-aa protein that showed the highest sequence similarity to C5aR from other species. Genomic analysis revealed the presence of one continuous exon encoding the entire open reading frame. Northern blot analysis showed significant expression of the trout C5a receptor (TC5aR) message in PBLs and kidney. Flow cytometric analysis showed that two Abs generated against two different areas of the extracellular N-terminal region of TC5aR positively stained the same leukocyte populations from PBLs. B lymphocytes and granulocytes comprised the majority of cells recognized by the anti-TC5aR. More importantly, these Abs inhibited chemotaxis of PBLs toward a chemoattractant fraction purified from complement-activated trout serum. Our data suggest that the split between C5aR and C3aR from a common ancestral molecule occurred before the emergence of teleost fish. Moreover, we demonstrate that the overall structure of C5aR as well as its role in chemotaxis have remained conserved for >300 million years.
Authors:
Hani Boshra; Jun Li; Rodney Peters; John Hansen; Anjan Matlapudi; J Oriol Sunyer
Related Documents :
22963323 - High depth, whole-genome sequencing of cholera isolates from haiti and the dominican re...
8024703 - Structure of the mouse gonadotropin-releasing hormone receptor gene: variant transcript...
18227253 - The copper-dependent ace1 transcription factor activates the transcription of the mco1 ...
Publication Detail:
Type:  Comparative Study; Journal Article; Research Support, U.S. Gov't, Non-P.H.S.    
Journal Detail:
Title:  Journal of immunology (Baltimore, Md. : 1950)     Volume:  172     ISSN:  0022-1767     ISO Abbreviation:  J. Immunol.     Publication Date:  2004 Apr 
Date Detail:
Created Date:  2004-03-22     Completed Date:  2004-07-30     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  2985117R     Medline TA:  J Immunol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  4381-90     Citation Subset:  AIM; IM    
Affiliation:
Department of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Data Bank Information
Bank Name/Acc. No.:
GENBANK/AY438032
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Amino Acid Sequence
Animals
Blotting, Northern
Blotting, Southern
Cell Migration Inhibition
Chemotaxis, Leukocyte / immunology*
Cloning, Molecular / methods
DNA, Complementary / isolation & purification
Gene Expression Regulation / immunology*
Humans
Immune Sera / pharmacology
Leukocytes / cytology,  immunology,  metabolism
Molecular Sequence Data
Oncorhynchus mykiss / genetics*,  immunology*
Protein Binding / immunology
Receptor, Anaphylatoxin C5a / genetics*,  immunology,  metabolism,  physiology
Sequence Analysis, DNA
Sequence Homology, Amino Acid
Chemical
Reg. No./Substance:
0/DNA, Complementary; 0/Immune Sera; 0/Receptor, Anaphylatoxin C5a

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Identification and molecular cloning of functional chicken IL-12.
Next Document:  Signaling through Toll-like receptors triggers HIV-1 replication in latently infected mast cells.