Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
1997-3-10
pubmed:abstractText
The insulin-like growth factors (IGFs) are known to stimulate both the proliferation and differentiation of neuroblastoma cells, but the role of the IGF binding proteins (IGFBPs) has not yet been established. In this study, human neuroblastoma SH-SY5Y cells have been treated with IGF-I and its potent analogue des(1-3)IGF-I alone or following preincubation with a differentiating agent such as 12-o-tetradecanoylphorbol-13-acetate (TPA). Cell proliferation and differentiation were evaluated. Conditioned medium was tested for the presence of IGFBPs by ligand blotting. The SH-SY5Y cell proliferation was maximally stimulated by des(1-3)IGF-I. The TPA-induced differentiation of SH-SY5Y, evaluated by assessment of cell morphology and GAP-43 expression as a biochemical marker of differentiation was potentiated by nanomolar concentrations of des(1-3)IGF-I and, to a smaller extent, IGF-I Conditioned medium showed the presence of a major IGFBP band with an approximate molecular weight of 32.5 kD and a very faint band of approximately 24kD. The IGFBP immunoblotting results suggest that the predominant band might represent IGFBP-2. Our data represent a first demonstration of the presence of IGFBPs in conditioned medium of human neuroblastoma SH-SY5Y cells. The finding that the potent IGF-I analogue des(1-3)IGF-I with reduced affinity for IGFBPs induce major effects on cell growth and differentiation suggests that the IGFBPs may play an active role in the neuronal response to the proliferative and differentiative effects of IGF-I.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Monoclonal, http://linkedlifedata.com/resource/pubmed/chemical/Culture Media, Serum-Free, http://linkedlifedata.com/resource/pubmed/chemical/GAP-43 Protein, http://linkedlifedata.com/resource/pubmed/chemical/Immune Sera, http://linkedlifedata.com/resource/pubmed/chemical/Insulin-Like Growth Factor Binding..., http://linkedlifedata.com/resource/pubmed/chemical/Insulin-Like Growth Factor I, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Glycoproteins, http://linkedlifedata.com/resource/pubmed/chemical/Nerve Tissue Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Neurofilament Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Peptide Fragments, http://linkedlifedata.com/resource/pubmed/chemical/Tetradecanoylphorbol Acetate, http://linkedlifedata.com/resource/pubmed/chemical/insulin-like growth factor 1...
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0804-4643
pubmed:author
pubmed:issnType
Print
pubmed:volume
135
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
716-23
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:9025718-Animals, pubmed-meshheading:9025718-Antibodies, Monoclonal, pubmed-meshheading:9025718-Cell Count, pubmed-meshheading:9025718-Cell Differentiation, pubmed-meshheading:9025718-Cell Division, pubmed-meshheading:9025718-Culture Media, Serum-Free, pubmed-meshheading:9025718-Electrophoresis, Polyacrylamide Gel, pubmed-meshheading:9025718-GAP-43 Protein, pubmed-meshheading:9025718-Humans, pubmed-meshheading:9025718-Immune Sera, pubmed-meshheading:9025718-Immunoblotting, pubmed-meshheading:9025718-Insulin-Like Growth Factor Binding Proteins, pubmed-meshheading:9025718-Insulin-Like Growth Factor I, pubmed-meshheading:9025718-Membrane Glycoproteins, pubmed-meshheading:9025718-Mice, pubmed-meshheading:9025718-Microscopy, Phase-Contrast, pubmed-meshheading:9025718-Nerve Tissue Proteins, pubmed-meshheading:9025718-Neuroblastoma, pubmed-meshheading:9025718-Neurofilament Proteins, pubmed-meshheading:9025718-Peptide Fragments, pubmed-meshheading:9025718-Tetradecanoylphorbol Acetate, pubmed-meshheading:9025718-Time Factors, pubmed-meshheading:9025718-Tumor Cells, Cultured
pubmed:year
1996
pubmed:articleTitle
Do insulin-like growth factor binding proteins (IGFBPs) modulate the IGF-I growth promoting and differentiating effects in human neuroblastoma cells?
pubmed:affiliation
Department of Paediatrics, Tor Vergata University, Rome, Italy.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, Non-U.S. Gov't