Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UNIPROT:P39060 (
endostatin
)
2,284
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Endostatin has attracted considerable attention because of its ability to inhibit angiogenesis. This property of monomeric
endostatin
contrasts with that of the trimeric
endostatin
moiety generated from the intact C-terminal domain of
collagen XVIII
that induces a promigratory phenotype in endothelial cells. This activity is inhibited by monomeric
endostatin
. In this study we demonstrate that the effect of oligomeric
endostatin
can also be inhibited by exogenous glycosaminoglycans in a size-dependent manner, with heparin oligosaccharides containing more than 20 monosaccharide residues having optimal inhibitory activity. Oligomeric
endostatin
was also found to induce morphological changes in Chinese hamster ovary cells, an epithelial cell line. This novel observation allowed the utilization of a panel of Chinese hamster ovary cell mutants with defined glycosaminoglycan biosynthetic defects. The action of oligomeric
endostatin
on these cells was shown to be dependent on cell surface glycosaminoglycans, principally heparan sulfate with N- and 6-O-sulfation of glucosamine residues rather than
iduronate
2-O-sulfation being important for bioactivity. The responsiveness of a cell line (pgsE-606) with globally reduced heparan sulfate sulfation and shortened S domains, however, indicates that overall heparan sulfate domain patterning is the key determinant of the bioactivity of oligomeric
endostatin
. Purified heparin-monomeric
endostatin
constructs generated by zero-length cross-linking techniques were found to be unable to inhibit the action of oligomeric
endostatin
. This indicates a mechanism for the perturbation of oligomeric
endostatin
action by its monomeric counterpart via competition for glycosaminoglycan attachment sites at the cell surface.
...
PMID:The morphogenic properties of oligomeric endostatin are dependent on cell surface heparan sulfate. 1648 16