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Updated: Oct 8, 2026

Directed Differentiation of Primitive and Definitive Hematopoietic Progenitors from Human Pluripotent Stem Cells
Published on: November 1, 2017
Pluripotent, erythrocytic and granulocytic hemopoietic precursors in chronic granulocytic leukemia
Insights
Chronic granulocytic leukemia (CGL) shows increased hemopoietic precursors due to higher marrow cell counts, not precursor concentration. Patients exhibit erythropoietin-independent erythropoietic bursts, suggesting regulatory defects in both granulocytic and erythrocytic cells.
Area of Science:
- Hematology
- Oncology
- Cell Biology
Background:
- Chronic granulocytic leukemia (CGL) is characterized by the Philadelphia chromosome (Ph1).
- Understanding the behavior of hemopoietic precursors in CGL is crucial for disease mechanisms.
Purpose of the Study:
- To investigate the behavior of committed and pluripotent hemopoietic precursors in CGL patients.
- To determine the role of erythropoietin (Ep) in erythropoiesis in CGL.
Main Methods:
- Methylcellulose culture techniques were used to analyze marrow and blood cells.
- Hemopoietic precursor concentrations and erythropoietin-independent bursts were assessed.
Main Results:
- CGL patients had significantly higher hemopoietic precursor concentrations per unit volume due to increased nucleated cell counts.
- Erythropoietin-independent BFU-E (burst-forming unit-erythroid) were observed in CGL marrow and blood.
- Peripheral blood showed increased CFUC, CFUE, BFUE, and CFUMIX correlating with leukocyte count.
Conclusions:
- Clonal expansion in CGL likely originates from pluripotent hemopoietic precursors.
- CFUMIX (committed and pluripotent hemopoietic precursors) can differentiate into CFUE (colony-forming unit-erythroid) in CGL.
- A regulatory defect affecting both granulocytic and erythrocytic cells is suggested in CGL.
Abstract:
Using methylcellulose culture techniques, we investigated the behavior of committed and pluripotent hemopoietic precursors (CFUMIX) in marrow cells and blood from patients with chronic granulocytic leukemia (CGL) in the chronic phase whose marrow cells showed the presence of Ph1 chromosomes. The relative concentrations of the marrow precursors in CGL were nearly equal to those in control patients. The mean nucleated cell count in marrow fluid from the patients, however, was 6.3 times that of control values. As a result, the mean concentrations per unit volume of the hemopoietic precursors in CGL were significantly higher than those in control patients. Furthermore, the presence of erythropoietin (Ep) independent BFUE giving rise to erythropoietic bursts in the medium without the addition of Ep was demonstrable in marrow cells and blood. In the peripheral blood, the increment in numbers of CFUC, CFUE, BFUE, and CFUMIX in accordance with the leucocyte count was observed. The present results are consistent with the theory that the clonal expansion in CGL occurs at the level of pluripotent hemopoietic precursors and suggest that CFUMIX in CGL can differentiate into CFUE along the erythropoietic pathway and that a regulatory defect in CGL in present in both granulocytic cells and erythrocytic cells.
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