Expansion of hematopoietic stem cells in the developing liver of a mouse embryo

H Ema, H Nakauchi - Blood, The Journal of the American …, 2000 - ashpublications.org
H Ema, H Nakauchi
Blood, The Journal of the American Society of Hematology, 2000ashpublications.org
The activity of hematopoietic stem cells in the developing liver of a C57BL/6 mouse embryo
was quantified by a competitive repopulation assay. Different doses of fetal liver cells at days
11 to 18 of gestation were transplanted into irradiated mice together with 2× 105 adult bone
marrow cells. A long-term repopulation in myeloid-, B-cell, and T-cell lineage by fetal liver
cells was evaluated at 20 weeks after transplantation. At day 12 of gestation multilineage
repopulating activity was first detected in the liver as 50 repopulating units (RU) per liver …
Abstract
The activity of hematopoietic stem cells in the developing liver of a C57BL/6 mouse embryo was quantified by a competitive repopulation assay. Different doses of fetal liver cells at days 11 to 18 of gestation were transplanted into irradiated mice together with 2 × 105 adult bone marrow cells. A long-term repopulation in myeloid-, B-cell, and T-cell lineage by fetal liver cells was evaluated at 20 weeks after transplantation. At day 12 of gestation multilineage repopulating activity was first detected in the liver as 50 repopulating units (RU) per liver. The number of RU per liver increased 10-fold and 33-fold by day 14 and day 16 of gestation, and decreased thereafter, suggesting a single wave of stem cell development in the fetal liver. A limiting dilution analysis revealed that the frequency of competitive repopulating units (CRU) in fetal liver cells at day 12 of gestation was similar to that at day 16 of gestation. Because of an increase of total fetal liver cell number, the absolute number of CRU per liver from days 12 to 16 of gestation increased 38-fold. Hence, the mean activity of stem cells (MAS) that is given by RU per CRU remained constant from days 12 to 16 of gestation. From these data we conclude that hematopoietic stem cells expand in the fetal liver maintaining their level of repopulating potential.
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