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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
|
pubmed:dateCreated |
1987-10-19
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pubmed:abstractText |
The binding of recombinant erythropoietin (EPO) to fetal mouse liver cells (FMLC) was investigated using a radioiodinated derivative which retained full biological activity. FMLC were fractionated using a preformed Percoll density gradient. Using the fractionated FMLC, the ability to form CFU-E colonies in a semisolid culture was examined, and the binding of [125I]EPO was measured. The highest specific binding of [125I]EPO was observed in a fraction with a density between 1.062 and 1.076 g/ml. The same fraction showed the highest ability to form CFU-E-derived colonies. After suspension culture of FMLC with EPO for 2 days, differentiated erythroid cells with higher density markedly increased. The specific binding of [125I]EPO to these cells almost disappeared with differentiation. Scatchard analysis with cells of the CFU-E-enriched fraction showed a nonlinear curve, suggesting the existence of two classes of binding sites. One binding site was high-affinity (Kd1 = 0.41 nM), and the other low-affinity (Kd2 = 3.13 nM). These results suggest that the expression of EPO receptors on the erythroid cells is highest in CFU-E.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0301-472X
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
15
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pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
833-7
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:3305053-Animals,
pubmed-meshheading:3305053-Cells, Cultured,
pubmed-meshheading:3305053-Cytological Techniques,
pubmed-meshheading:3305053-Erythropoietin,
pubmed-meshheading:3305053-Fetus,
pubmed-meshheading:3305053-Hematopoietic Stem Cells,
pubmed-meshheading:3305053-Iodine Radioisotopes,
pubmed-meshheading:3305053-Liver,
pubmed-meshheading:3305053-Mice
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pubmed:year |
1987
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pubmed:articleTitle |
Binding of erythropoietin to CFU-E derived from fetal mouse liver cells.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|