TY - JOUR
T1 - Hepatocyte growth factor is a potent angiogenic factor which stimulates endothelial cell motility and growth
AU - Bussolino, F.
AU - Di Renzo, M. F.
AU - Ziche, M.
AU - Bocchietto, E.
AU - Olivero, M.
AU - Naldini, L.
AU - Gaudino, G.
AU - Tamagnone, Luca
AU - Coffer, A.
AU - Comoglio, P. M.
PY - 1992
Y1 - 1992
N2 - Hepatocyte Growth Factor (HGF, also known as Scatter Factor) is a powerful mitogen or motility factor in different cells, acting through the tyrosine kinase receptor encoded by the MET protooncogene. Endothelial cells express the MET gene and expose at the cell surface the mature protein (p190MET) made of a 50 kD (alpha) subunit disulfide linked to a 145-kD (beta) subunit. HGF binding to endothelial cells identifies two sites with different affinities. The higher affinity binding site (Kd = 0.35 nM) corresponds to the p190MET receptor. Sub-nanomolar concentrations of HGF, but not of a recombinant inactive precursor, stimulate the receptor kinase activity, cell proliferation and motility. HGF induces repairs of a wound in endothelial cell monolayer. HGF stimulates the scatter of endothelial cells grown on three-dimensional collagen gels, inducing an elongated phenotype. In the rabbit cornea, highly purified HGF promotes neovascularization at sub-nanomolar concentrations. HGF lacks activities related to hemostasis-thrombosis, inflammation and endothelial cells accessory functions. These data show that HGF is an in vivo potent angiogenic factor and in vitro induces endothelial cells to proliferate and migrate.
PMID: 1383237 PMCID: PMC2289675 DOI: 10.1083/jcb.119.3.629
AB - Hepatocyte Growth Factor (HGF, also known as Scatter Factor) is a powerful mitogen or motility factor in different cells, acting through the tyrosine kinase receptor encoded by the MET protooncogene. Endothelial cells express the MET gene and expose at the cell surface the mature protein (p190MET) made of a 50 kD (alpha) subunit disulfide linked to a 145-kD (beta) subunit. HGF binding to endothelial cells identifies two sites with different affinities. The higher affinity binding site (Kd = 0.35 nM) corresponds to the p190MET receptor. Sub-nanomolar concentrations of HGF, but not of a recombinant inactive precursor, stimulate the receptor kinase activity, cell proliferation and motility. HGF induces repairs of a wound in endothelial cell monolayer. HGF stimulates the scatter of endothelial cells grown on three-dimensional collagen gels, inducing an elongated phenotype. In the rabbit cornea, highly purified HGF promotes neovascularization at sub-nanomolar concentrations. HGF lacks activities related to hemostasis-thrombosis, inflammation and endothelial cells accessory functions. These data show that HGF is an in vivo potent angiogenic factor and in vitro induces endothelial cells to proliferate and migrate.
PMID: 1383237 PMCID: PMC2289675 DOI: 10.1083/jcb.119.3.629
KW - HEPATOCYTE GROWTH FACTOR
KW - HEPATOCYTE GROWTH FACTOR
UR - http://hdl.handle.net/10807/141644
U2 - 10.1083/jcb.119.3.629
DO - 10.1083/jcb.119.3.629
M3 - Article
SN - 0021-9525
VL - 119
SP - 629
EP - 641
JO - THE JOURNAL OF CELL BIOLOGY
JF - THE JOURNAL OF CELL BIOLOGY
ER -