Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
15
pubmed:dateCreated
1993-6-24
pubmed:databankReference
pubmed:abstractText
Radioiodinated erythropoietin (Epo) was bound specifically to the cells of two non-erythroid clonal lines, PC12 and SN6, which expressed neuronal characteristics. The binding was time-, cell number-, and dose-dependent and was reversible. Although the cloned Epo receptor from PC12 cells (derived from rat adrenal medulla) was identical to that from rat erythroid cells, significant differences in the ligand binding properties between two cell lineages were found; 1) PC12 cells had a single class of binding sites with very low affinity (Kd = 16 nM), whereas erythroid cells had two classes of binding sites with different affinities (Kd = 95 pM for high affinity sites and 1.9 nM for low affinity sites), and 2) cross-linking experiments revealed one cross-linked product of 105 kDa for PC12 cells and two products of 140 and 120 kDa for erythroid cells. Taken together with additional results, the presence of a putative accessory protein(s) that may alter the ligand binding affinity through interaction with Epo receptor is discussed. The binding of Epo to PC12 cells caused a rapid increase in the cytosolic concentration of free calcium. The presence of EGTA had no effect on the Epo binding but completely inhibited the calcium increase, indicating that Epo stimulated the calcium influx from outside of the cells. The addition of Epo to the culture media of PC12 cells elevated the intracellular concentrations of monoamines.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0021-9258
pubmed:author
pubmed:issnType
Print
pubmed:day
25
pubmed:volume
268
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
11208-16
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:7684373-Adrenal Medulla, pubmed-meshheading:7684373-Amino Acid Sequence, pubmed-meshheading:7684373-Animals, pubmed-meshheading:7684373-Base Sequence, pubmed-meshheading:7684373-Biogenic Amines, pubmed-meshheading:7684373-Blotting, Northern, pubmed-meshheading:7684373-Calcium, pubmed-meshheading:7684373-Cells, Cultured, pubmed-meshheading:7684373-DNA, pubmed-meshheading:7684373-Erythropoietin, pubmed-meshheading:7684373-Humans, pubmed-meshheading:7684373-Kinetics, pubmed-meshheading:7684373-Liver, pubmed-meshheading:7684373-Mice, pubmed-meshheading:7684373-Molecular Sequence Data, pubmed-meshheading:7684373-Neurons, pubmed-meshheading:7684373-Oligodeoxyribonucleotides, pubmed-meshheading:7684373-PC12 Cells, pubmed-meshheading:7684373-Polymerase Chain Reaction, pubmed-meshheading:7684373-RNA, pubmed-meshheading:7684373-RNA, Messenger, pubmed-meshheading:7684373-Rats, pubmed-meshheading:7684373-Receptors, Erythropoietin, pubmed-meshheading:7684373-Recombinant Proteins, pubmed-meshheading:7684373-Sequence Homology, Amino Acid, pubmed-meshheading:7684373-Spleen
pubmed:year
1993
pubmed:articleTitle
Functional erythropoietin receptor of the cells with neural characteristics. Comparison with receptor properties of erythroid cells.
pubmed:affiliation
Department of Food Science and Technology, Faculty of Agriculture, Kyoto University, Japan.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, Non-U.S. Gov't