The role of hypoxia in the maintenance of hematopoietic stem cells.

Bone marrow cell liquid cultures were incubated at various oxygen concentrations ranging from 0% to 18% (air). The total number of cells in culture (CT) at the end of a 6-day incubation was found to be directly proportional to the oxygen concentration. As compared with air-incubated controls, cells recovered from severely hypoxic (1% oxygen) day-5 liquid cultures showed (1) the same day-7 colony-formation efficiency in semisolid culture (neutrophilic/monocytic colonies) or in spleen; (2) a higher day-14 spleen colony-formation efficiency; (3) an enhanced radio-protection ability; and (4) an increased marrow repopulation ability, as measured by determining either total cell number in recipient marrow MRAcell, or the capacity of the latter of generating day-7 neutrophilic/monocytic colonies in secondary in vitro assays (MRACFU-NM). Taking into account CT, the absolute numbers of progenitors in culture were also computed. The results showed that, with respect to time 0, incubation in air produced an increase in the number of day-7 CFUs and a decrease in the number of the other progenitors, whereas in hypoxic cultures all types of progenitors decreased. However, as compared with air-incubated controls, all progenitors, except cells sustaining MRACFU-NM, were reduced in hypoxic cultures. The degree of reduction paralleled the position of the progenitor in the hematopoietic hierarchy, being maximum for day-7 CFUs and null for cells sustaining MRACFU-NM, which, in fact, were better preserved in hypoxic cultures.

[1]  G. Spangrude,et al.  Resting and activated subsets of mouse multipotent hematopoietic stem cells. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[2]  C. Langefeld,et al.  Enhanced stimulation of human bone marrow macrophage colony formation in vitro by recombinant human macrophage colony-stimulating factor in agarose medium and at low oxygen tension. , 1990, Blood.

[3]  J. Visser,et al.  Purification of pluripotent hemopoietic stem cells: past and present. , 1990, Experimental hematology.

[4]  J. Hendry,et al.  The development of spatial distributions of CFU‐S and in‐vitro CFC in femora of mice of different ages , 1989, British journal of haematology.

[5]  R. Ploemacher,et al.  Separation of CFU-S from primitive cells responsible for reconstitution of the bone marrow hemopoietic stem cell compartment following irradiation: evidence for a pre-CFU-S cell. , 1989, Experimental hematology.

[6]  E. Nečas,et al.  A comparison of stem cell assays using early or late spleen colonies , 1989, Cell and tissue kinetics.

[7]  N. Brons,et al.  In vivo proliferative and differential properties of murine bone marrow cells separated on the basis of rhodamine-123 retention. , 1988, Experimental hematology.

[8]  N. Brons,et al.  Cells with marrow and spleen repopulating ability and forming spleen colonies on day 16, 12, and 8 are sequentially ordered on the basis of increasing rhodamine 123 retention , 1988, Journal of cellular physiology.

[9]  Y. Ishikawa,et al.  Kinetics of hemopoietic stem cells in a hypoxic culture , 1988, European journal of haematology.

[10]  M. Olivotto,et al.  Hemopoietic progenitor cells are sensitive to the cytostatic effect of pyruvate. , 1987, Experimental hematology.

[11]  H. Lin,et al.  Modulation of tissue mononuclear phagocyte clonal growth by oxygen and antioxidant enzymes. , 1986, Experimental hematology.

[12]  H. Broxmeyer,et al.  Comparative influences of phytohemagglutinin-stimulated leukocyte conditioned medium, hemin, prostaglandin E, and low oxygen tension on colony formation by erythroid progenitor cells in normal human bone marrow. , 1985, Experimental hematology.

[13]  I. Bertoncello,et al.  Multiparameter analysis of transplantable hemopoietic stem cells: I. The separation and enrichment of stem cells homing to marrow and spleen on the basis of rhodamine-123 fluorescence. , 1985, Experimental hematology.

[14]  T. Dexter,et al.  Haemopoietic cell growth factor and glucose transport. Its role in cell survival and the relevance of this in normal haemopoiesis and leukaemia. , 1984, Differentiation; research in biological diversity.

[15]  Hodgson Gs,et al.  In vivo kinetic status of hematopoietic stem and progenitor cells as inferred from labeling with bromodeoxyuridine. , 1984 .

[16]  A. Balin,et al.  Oxygen modulates growth of human cells at physiologic partial pressures , 1984, The Journal of experimental medicine.

[17]  M. Olivotto,et al.  Metabolic Aspects of Cell Cycle Regulation in Normal and Cancer Cells , 1984, Toxicologic pathology.

[18]  G. van Zant,et al.  Studies of hematopoietic stem cells spared by 5-fluorouracil , 1984, The Journal of experimental medicine.

[19]  G. Zant Studies of hematopoietic stem cells spared by 5-fluorouracil. , 1984 .

[20]  T. Dexter,et al.  Haemopoietic cell growth factor mediates cell survival via its action on glucose transport. , 1984, The EMBO journal.

[21]  M. Olivotto,et al.  The respiration‐linked limiting step of tumor cell transition from the non‐cycling to the cycling state: Its inhibition by oxidizable substrates and its relationships to purine metabolism , 1983, Journal of cellular physiology.

[22]  T. Dexter,et al.  Effect of haematopoietic cell growth factor on intracellular ATP levels , 1983, Nature.

[23]  B. Kubanek,et al.  The effect of reduced oxygen tension on colony formation of erythropoietic cells in vitro , 1982, British journal of haematology.

[24]  M. Olivotto,et al.  The role of respiration in tumor cell transition from the noncycling to the cycling state , 1981, Journal of cellular physiology.

[25]  M. Lichtman The ultrastructure of the hemopoietic environment of the marrow: a review. , 1981, Experimental hematology.

[26]  M L Walsh,et al.  Monitoring of relative mitochondrial membrane potential in living cells by fluorescence microscopy , 1981, The Journal of cell biology.

[27]  L. Oberley,et al.  Cell differentiation, aging and cancer: the possible roles of superoxide and superoxide dismutases. , 1980, Medical hypotheses.

[28]  G. Hodgson,et al.  Properties of haematopoietic stem cells surviving 5-fluorouracil treatment: evidence for a pre-CFU-S cell? , 1979, Nature.

[29]  L. Lajtha,et al.  A comparison of cell replacement in bone marrow, testis and three regions of surface epithelium. , 1979, Biochimica et biophysica acta.

[30]  G. Hodgson,et al.  The effect of oxygen tension on haemopoietic and fibroblast cell proliferation in vitro , 1978, Journal of cellular physiology.

[31]  K. Sanford,et al.  Density‐dependent effects of oxygen on the growth of mammalian fibroblasts in culture , 1978, Journal of cellular physiology.

[32]  S. Shackney,et al.  KINETIC‐MICROARCHITECTURAL CORRELATIONS IN THE BONE MARROW OF THE MOUSE , 1975, Cell and tissue kinetics.

[33]  H. M. Patt,et al.  Biochemical studies of cytokinetic changes during tumor growth. , 1970, Cancer research.

[34]  I. Tannock The relation between cell proliferation and the vascular system in a transplanted mouse mammary tumour. , 1968, British journal of cancer.

[35]  I. Tannock,et al.  THE RELATION BETWEEN CELL PROLIFERATION AND THE VASCULAR SYSTEM IN A TRANSPLANTED MOUSE MAMMARY TUMOUR , 2007 .

[36]  B. Lord The architecture of bone marrow cell populations. , 1990, International journal of cell cloning.

[37]  N. Brons,et al.  Isolation of hemopoietic stem cell subsets from murine bone marrow: II. Evidence for an early precursor of day-12 CFU-S and cells associated with radioprotective ability. , 1988, Experimental hematology.

[38]  N. Brons,et al.  Isolation of hemopoietic stem cell subsets from murine bone marrow: I. Radioprotective ability of purified cell suspensions differing in the proportion of day-7 and day-12 CFU-S. , 1988, Experimental hematology.

[39]  M. Allalunis-Turner,et al.  Growth of murine bone marrow under various oxygen conditions in media buffered with HEPES. , 1987, International journal of cell cloning.

[40]  J. Visser,et al.  Separation and functional analysis of bone marrow cells separated by rhodamine-123 fluorescence. , 1987, Experimental hematology.

[41]  G. Hodgson,et al.  In vivo kinetic status of hematopoietic stem and progenitor cells as inferred from labeling with bromodeoxyuridine. , 1984, Experimental hematology.

[42]  G. Hodgson,et al.  The organization of hemopoietic tissue as inferred from the effects of 5-fluorouracil. , 1982, Experimental hematology.

[43]  R. Schofield The relationship between the spleen colony-forming cell and the haemopoietic stem cell. , 1978, Blood cells.

[44]  J. Hendry,et al.  The relative spatial distributions of CFUs and CFUc in the normal mouse femur. , 1975, Blood.