Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1-2
pubmed:dateCreated
2001-11-5
pubmed:abstractText
Calcitonin gene-related peptide (CGRP) and adrenomedullin (ADM), two closely related peptides, initiate their biological responses through their interaction with calcitonin receptor-like receptor (CRLR). The CRLR receptor phenotype can be determined by coexpression of CRLR with one of the three-receptor activity modifying proteins (RAMPs). In this report, we characterized the pharmacological properties of the human or porcine CRLR with individual RAMPs transiently expressed in human embryonic kidney cell line (HEK-293). Characterization of RAMP1/human or porcine CRLR combination by radioligand binding ([125I] halphaCGRP) and functional assay (activation of adenylyl cyclase) revealed the properties of CGRP receptor. Similarly characterization of RAMP2/human or porcine CRLR and RAMP3/human or porcine CRLR combination by radioligand binding ([125I] rADM) and functional assay (activation of adenylyl cyclase) revealed the properties of ADM (22-52) sensitive-ADM receptor. In addition, porcine CRLR/RAMP2 or 3 combination displayed specific high affinity [125I] halphaCGRP binding also. Also, co-transfection of porcine CRLR with RAMPs provided higher expression level of the receptor than the human counterpart. Thus the present study along with earlier studies strongly support the role of RAMPs in the functional expression of specific CRLRs.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Adenylate Cyclase, http://linkedlifedata.com/resource/pubmed/chemical/Adrenomedullin, http://linkedlifedata.com/resource/pubmed/chemical/CALCRL protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Calcitonin Receptor-Like Protein, http://linkedlifedata.com/resource/pubmed/chemical/Intracellular Signaling Peptides..., http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Peptides, http://linkedlifedata.com/resource/pubmed/chemical/RAMP1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/RAMP2 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/RAMP3 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Receptor Activity-Modifying..., http://linkedlifedata.com/resource/pubmed/chemical/Receptor Activity-Modifying..., http://linkedlifedata.com/resource/pubmed/chemical/Receptor Activity-Modifying..., http://linkedlifedata.com/resource/pubmed/chemical/Receptor Activity-Modifying Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Calcitonin
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0300-8177
pubmed:author
pubmed:issnType
Print
pubmed:volume
224
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
123-33
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:11693189-Adenylate Cyclase, pubmed-meshheading:11693189-Adrenomedullin, pubmed-meshheading:11693189-Animals, pubmed-meshheading:11693189-Binding, Competitive, pubmed-meshheading:11693189-Calcitonin Receptor-Like Protein, pubmed-meshheading:11693189-Cell Line, pubmed-meshheading:11693189-Humans, pubmed-meshheading:11693189-Intracellular Signaling Peptides and Proteins, pubmed-meshheading:11693189-Membrane Proteins, pubmed-meshheading:11693189-Peptides, pubmed-meshheading:11693189-Protein Binding, pubmed-meshheading:11693189-Receptor Activity-Modifying Protein 1, pubmed-meshheading:11693189-Receptor Activity-Modifying Protein 2, pubmed-meshheading:11693189-Receptor Activity-Modifying Protein 3, pubmed-meshheading:11693189-Receptor Activity-Modifying Proteins, pubmed-meshheading:11693189-Receptors, Calcitonin, pubmed-meshheading:11693189-Swine, pubmed-meshheading:11693189-Transfection
pubmed:year
2001
pubmed:articleTitle
Receptor activity modifying proteins interaction with human and porcine calcitonin receptor-like receptor (CRLR) in HEK-293 cells.
pubmed:affiliation
Department of Cardiovascular Pharmacology, GlaxoSmithKline, King of Prussia, PA 19406-0939, USA.
pubmed:publicationType
Journal Article