Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
46
pubmed:dateCreated
2001-11-13
pubmed:databankReference
pubmed:abstractText
Five G protein-coupled receptors (S1P(1)/Edg-1, S1P(3)/Edg-3, S1P(2)/Edg-5, S1P(4)/Edg-6, and S1P(5)/Edg-8) for the intercellular lipid mediator sphingosine 1-phosphate have been cloned and characterized. We found human and mouse sequences closely related to rat S1P(5) (97% identical amino acids) and report now the characterization of the human and mouse S1P(5) gene products as encoding sphingosine 1-phosphate receptors. When HEK293T cells were cotransfected with S1P(5) and G protein DNAs, prepared membranes showed sphingosine 1-phosphate concentration-dependent increases in [gamma-(35)S]GTP binding (EC(50) = 12.7 nM). The lipid mediator inhibited forskolin-driven rises in cAMP by greater than 80% after introduction of the mouse or human S1P(5) DNAs into rat hepatoma RH7777 cells (IC(50) = 0.22 nM). This response is blocked fully by prior treatment of cultures with pertussis toxin, thus implicating signaling through G(i/o)alpha proteins. Northern blot analysis showed high expression of human S1P(5) mRNA in spleen, corpus collosum, peripheral blood leukocytes, placenta, lung, aorta, and fetal tissues. Mouse S1P(5) mRNA is also expressed in spleen and brain. Finally, we found that one enantiomer of a sphingosine 1-phosphate analogue wherein the 3-hydroxyl and 4,5-olefin are replaced by an amide functionality shows some selectivity as an agonist S1P(1) and S1P(3) vs S1P(2) and S1P(5).
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0006-2960
pubmed:author
pubmed:issnType
Print
pubmed:day
20
pubmed:volume
40
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
14053-60
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:11705398-Amino Acid Sequence, pubmed-meshheading:11705398-Animals, pubmed-meshheading:11705398-Cell Line, pubmed-meshheading:11705398-Cloning, Molecular, pubmed-meshheading:11705398-Gene Expression Regulation, pubmed-meshheading:11705398-Humans, pubmed-meshheading:11705398-Lysophospholipids, pubmed-meshheading:11705398-Mice, pubmed-meshheading:11705398-Molecular Sequence Data, pubmed-meshheading:11705398-Organ Specificity, pubmed-meshheading:11705398-RNA, Messenger, pubmed-meshheading:11705398-Rats, pubmed-meshheading:11705398-Receptors, Cell Surface, pubmed-meshheading:11705398-Receptors, G-Protein-Coupled, pubmed-meshheading:11705398-Receptors, Lysophospholipid, pubmed-meshheading:11705398-Sphingosine, pubmed-meshheading:11705398-Structure-Activity Relationship, pubmed-meshheading:11705398-Transfection, pubmed-meshheading:11705398-Tumor Cells, Cultured, pubmed-meshheading:11705398-Zebrafish
pubmed:year
2001
pubmed:articleTitle
Characterization of the human and mouse sphingosine 1-phosphate receptor, S1P5 (Edg-8): structure-activity relationship of sphingosine1-phosphate receptors.
pubmed:affiliation
Department of Pharmacology, University of Virginia, 1300 Jefferson Park Avenue, Charlottesville, Virginia 22908, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't