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.
机构:
CARDINAL GLENNON CHILDRENS HOSP, PEDIAT RES INST, DEPT PEDIAT, ST LOUIS, MO USACARDINAL GLENNON CHILDRENS HOSP, PEDIAT RES INST, DEPT PEDIAT, ST LOUIS, MO USA
NOGUCHI, A
ENSOR, N
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机构:
CARDINAL GLENNON CHILDRENS HOSP, PEDIAT RES INST, DEPT PEDIAT, ST LOUIS, MO USACARDINAL GLENNON CHILDRENS HOSP, PEDIAT RES INST, DEPT PEDIAT, ST LOUIS, MO USA
ENSOR, N
NJEVILS, M
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CARDINAL GLENNON CHILDRENS HOSP, PEDIAT RES INST, DEPT PEDIAT, ST LOUIS, MO USACARDINAL GLENNON CHILDRENS HOSP, PEDIAT RES INST, DEPT PEDIAT, ST LOUIS, MO USA