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Myeloerythroid-restricted Progenitors Are Sufficient to Confer Radioprotection and Provide the Majority of Day 8 CFU-S

Overview
Journal J Clin Invest
Specialty General Medicine
Date 2002 Jun 19
PMID 12070305
Citations 81
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Abstract

Whole-body irradiation at the minimal lethal dose causes bone marrow failure and death within 12-18 days. To identify the principal components of the hematopoietic system that are radioprotective, we transplanted lethally irradiated mice with purified progenitors: common myeloid progenitors (CMPs), megakaryocyte/erythrocyte-restricted progenitors (MEPs), or granulocyte/monocyte-restricted progenitors (GMPs). Transplanted CMPs gave rise to cells both of the granulocyte/monocyte (GM) series and the megakaryocyte/erythrocyte series, whereas GMPs or MEPs showed reconstitution of only GM or ME cells, respectively. CMPs and MEPs but not GMPs protected mice in a dose-dependent manner, suggesting that erythrocytes, platelets, or both are the critical effectors of radioprotection. Accordingly, CMPs and MEPs formed robust colonies in recipient bone marrow and spleen, whereas GMPs formed small colonies that rapidly disappeared. Direct comparisons of spleen CFU (CFU-S) potentials among each progenitor subset showed that MEPs contain the vast majority of day 8 CFU-S activity, suggesting that day 8 CFU-S are the precursors of radioprotective cell subsets. All animals radioprotected for 30 days subsequently survived for at least 6 months post-transplant, and showed only host-derived hematopoiesis after 30 days. These findings suggest that rare hematopoietic stem cells survive myeloablation that can eventually repopulate irradiated hosts if myeloerythroid-restricted progenitors transiently rescue ablated animals through the critical window of bone marrow failure.

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References
1.
Spangrude G, Heimfeld S, Weissman I . Purification and characterization of mouse hematopoietic stem cells. Science. 1988; 241(4861):58-62. DOI: 10.1126/science.2898810. View

2.
Johnson G, Metcalf D . Pure and mixed erythroid colony formation in vitro stimulated by spleen conditioned medium with no detectable erythropoietin. Proc Natl Acad Sci U S A. 1977; 74(9):3879-82. PMC: 431768. DOI: 10.1073/pnas.74.9.3879. View

3.
Ichikawa Y, PLUZNIK D, Sachs L . In vitro control of the development of macrophage and granulocyte colonies. Proc Natl Acad Sci U S A. 1966; 56(2):488-95. PMC: 224399. DOI: 10.1073/pnas.56.2.488. View

4.
Bradley T, Metcalf D . The growth of mouse bone marrow cells in vitro. Aust J Exp Biol Med Sci. 1966; 44(3):287-99. DOI: 10.1038/icb.1966.28. View

5.
Metcalf D, Johnson G, Mandel T . Colony formation in agar by multipotential hemopoietic cells. J Cell Physiol. 1979; 98(2):401-20. DOI: 10.1002/jcp.1040980216. View