Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
1992-8-20
pubmed:abstractText
K-252b, a protein kinase inhibitor, has been shown earlier to inhibit nerve growth factor actions on cholinergic neurons of the basal forebrain. In the present study, K-252b was found to prevent trophic actions of two other neurotrophins, brain-derived neurotrophic factor, and neurotrophin-3, on central cholinergic and dopaminergic neurons, peripheral sensory neurons, and PC12 pheochromocytoma cells, when used at greater than 2 microM concentration. Comparable actions of nonneurotrophin growth factors were not affected. Surprisingly, at 0.1-100 nM, K-252b selectively enhanced the trophic action of neurotrophin-3 on central cholinergic neurons, peripheral sensory neurons, and PC12 cells. In PC12 cells, K-252b potentiated the neurotrophin-3-induced tyrosine phosphorylation of trk, a protein kinase responsible for transmitting neurotrophin signals. Of the three structurally related nerve growth factor inhibitors, K-252a, K-252b, and staurosporine, only the first two also mediated neurotrophin-3 potentiation. These findings indicate that K-252b generally and selectively potentiates the neurotrophic action of neurotrophin-3 and suggest that this action involves trk-type neurotrophin receptors.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Alkaloids, http://linkedlifedata.com/resource/pubmed/chemical/Brain-Derived Neurotrophic Factor, http://linkedlifedata.com/resource/pubmed/chemical/Carbazoles, http://linkedlifedata.com/resource/pubmed/chemical/Indole Alkaloids, http://linkedlifedata.com/resource/pubmed/chemical/Nerve Growth Factors, http://linkedlifedata.com/resource/pubmed/chemical/Nerve Tissue Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Neurotrophin 3, http://linkedlifedata.com/resource/pubmed/chemical/Protein Kinase C, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Receptor, trkA, http://linkedlifedata.com/resource/pubmed/chemical/Staurosporine, http://linkedlifedata.com/resource/pubmed/chemical/Tyrosine, http://linkedlifedata.com/resource/pubmed/chemical/staurosporine aglycone
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0022-3042
pubmed:author
pubmed:issnType
Print
pubmed:volume
59
pubmed:geneSymbol
trk
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
715-22
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:1629741-Adrenal Gland Neoplasms, pubmed-meshheading:1629741-Alkaloids, pubmed-meshheading:1629741-Animals, pubmed-meshheading:1629741-Brain-Derived Neurotrophic Factor, pubmed-meshheading:1629741-Carbazoles, pubmed-meshheading:1629741-Cells, Cultured, pubmed-meshheading:1629741-Chick Embryo, pubmed-meshheading:1629741-Dose-Response Relationship, Drug, pubmed-meshheading:1629741-Indole Alkaloids, pubmed-meshheading:1629741-Nerve Growth Factors, pubmed-meshheading:1629741-Nerve Tissue Proteins, pubmed-meshheading:1629741-Neurons, pubmed-meshheading:1629741-Neurons, Afferent, pubmed-meshheading:1629741-Neurotrophin 3, pubmed-meshheading:1629741-Pheochromocytoma, pubmed-meshheading:1629741-Phosphorylation, pubmed-meshheading:1629741-Protein Kinase C, pubmed-meshheading:1629741-Proto-Oncogene Proteins, pubmed-meshheading:1629741-Rats, pubmed-meshheading:1629741-Receptor, trkA, pubmed-meshheading:1629741-Signal Transduction, pubmed-meshheading:1629741-Staurosporine, pubmed-meshheading:1629741-Tumor Cells, Cultured, pubmed-meshheading:1629741-Tyrosine
pubmed:year
1992
pubmed:articleTitle
K-252b selectively potentiates cellular actions and trk tyrosine phosphorylation mediated by neurotrophin-3.
pubmed:affiliation
Department of Biological Sciences, University of Southern California, Los Angeles 90089.
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