| Literature DB >> 1312022 |
S Masuda1, Y Hisada, R Sasaki.
Abstract
Erythropoietin (EPO) stimulates proliferation and differentiation of late erythroid precursor cells (CFU-E) and thereby determines the rate of erythropoiesis. Liver is the major erythropoietic site in a fetus. We dealt with developmental changes in CFU-E and EPO receptor (EPO-R) of fetal mouse liver. The affinity of the EPO-R to EPO was unchanged during fetal development. The population size of CFU-E, the number of EPO-R per liver cell, and EPO-R mRNA decreased as gestation proceeded, in a pattern indicating that the expression of EPO-R on erythroid precursor cells in fetal mouse liver is governed mostly by the process of mRNA production.Entities:
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Year: 1992 PMID: 1312022 DOI: 10.1016/0014-5793(92)80048-l
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124