Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
1995-1-26
pubmed:abstractText
Heparin is required for fibroblast growth factor (FGF) stimulation of biological responses. Using isothermal titration calorimetry, we show that acidic FGF (aFGF) forms a 1:1 complex with the soluble extracellular domain of FGF receptor (FGFR). Heparin exerts its effect by binding to many molecules of aFGF. The resulting aFGF-heparin complex can bind to several receptor molecules, leading to FGFR dimerization. In two cell lines lacking endogenous heparan sulfate, exogenous heparin is required for FGFR dimerization, tyrosine kinase activation, c-fos mRNA transcription, and cell proliferation. Moreover, a synthetic heparin analog that binds monovalently to aFGF blocks FGFR dimerization, activation, and signaling via FGFR. We propose that heparin causes oligomerization of aFGF such that its binding to FGFR results in dimerization and activation. This represents a novel mechanism for transmembrane signaling and may account for the action of many heparin-bound growth factors.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0092-8674
pubmed:author
pubmed:issnType
Print
pubmed:day
16
pubmed:volume
79
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1015-24
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:7528103-Animals, pubmed-meshheading:7528103-CHO Cells, pubmed-meshheading:7528103-Calorimetry, pubmed-meshheading:7528103-Cell Division, pubmed-meshheading:7528103-Cricetinae, pubmed-meshheading:7528103-Enzyme Activation, pubmed-meshheading:7528103-Fibroblast Growth Factor 1, pubmed-meshheading:7528103-Heparin, pubmed-meshheading:7528103-Models, Biological, pubmed-meshheading:7528103-Phosphorylation, pubmed-meshheading:7528103-Protein Binding, pubmed-meshheading:7528103-Protein Conformation, pubmed-meshheading:7528103-Protein-Tyrosine Kinases, pubmed-meshheading:7528103-Proto-Oncogene Proteins c-fos, pubmed-meshheading:7528103-RNA, Messenger, pubmed-meshheading:7528103-Receptors, Fibroblast Growth Factor, pubmed-meshheading:7528103-Recombinant Proteins, pubmed-meshheading:7528103-Signal Transduction
pubmed:year
1994
pubmed:articleTitle
Heparin-induced oligomerization of FGF molecules is responsible for FGF receptor dimerization, activation, and cell proliferation.
pubmed:affiliation
Department of Pharmacology, New York University Medical Center, New York 10016.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, U.S. Gov't, Non-P.H.S., Research Support, Non-U.S. Gov't