PubMed · 1977 · 21 citations · 0 references
Life SciencesBiologyHematologyCell DifferentiationCell ProliferationStem Cell BiologyBlood Cell DifferentiationBone Marrow PhysiologyHematopoietic DevelopmentHematopoietic DifferentiationHematopoietic Stem Cell BiologyHematopoietic Stem CellsHematopoietic Stem Cell DevelopmentHematopoietic Stem Cell DifferentiationHematopoietic Stem Cell MaintenanceHematopoietic Stem Cell ProliferationHemopoietic Stem Cell Commitment
89Sr was used to ablate the marrows of 12- to 16-week-old CAF1 mice. The CFU-S of their blood, marrows, and spleens were assayed at intervals from days 10 through 56. The effects of splenectomy performed on day 14 or 42 on the numbers of CFU-S in the blood and marrow were also studied. On day 10 after treatment with 89Sr both the cellularity and CFU-S of the marrow were markedly decreased. Later, especially during the third week after treatment, marrow cellularity increased and by day 56 had returned to 74 percent of normal; the concentration of marrow CFU-S also increased but by day 56 had attained a level of only one-third normal. Thus, replenishment of the marrow's CFU-S lagged behind the repletion of its cellularity. Spleen and blood CFU-S were elevated throughout the 56 days. The number of splenic CFU-S was highest at day 10, decreased somewhat by day 21, and remained remarkably stable thereafter. After splenectomy there was a significant decline in the content of both blood and marrow CFU-S, whereas the reverse occurred in the "cold" 88Sr-treated control group. The results of these studies suggest that in the 89Sr-irradiated animal the spleen is transformed from a trapper to the prime supplier of CFU-S and that in normal mice the spleen may suppress marrow CFU-S proliferation. An inverse relationship between the size of the pool of mature granulocytes and the number of CFU-S was found, suggesting that the granulocyte compartment may, at least in part, play a role in the regulation of CFU-S proliferation.