Thermal sensitivity of the murine CFU-S-12: Role of environmental cells

References

• Baeza F., Bueren J. A., Maganto G. Differential sensitivity to hyperthermia of mouse normal haemopoietic stem cells related to proliferation activity and organ source. International Journal of Hyperthermia 1987; 3: 365–377
   PubMed Web of Science ®Google Scholar
• Chertkov J. L., Drize N. J., Gurevitch O. A., Udalov G. A. Cells responsible for restoration of haemopoiesis in long-term murine bone marrow culture. Leukemia Research 1986; 10: 659–663
   PubMedGoogle Scholar
• Curry J. L., Trentin J. J. Hemopoietic spleen colony studies. I. Growth and differentiation. Developmental Biology 1967; 15: 395–413
   PubMed Web of Science ®Google Scholar
• Elkon D., Sabio H., McGrath E., Baker D. G. Temperature dependent inhibition of murine granulocyte-monocyte precursors. Cancer Research 1981; 41: 1812–1816
   PubMed Web of Science ®Google Scholar
• Field S. B. Hyperthermia in the treatment of cancer. Physics in Medicine and Biology 1987; 32: 789–811
   PubMed Web of Science ®Google Scholar
• Flentje M., Flentje D., Sapareto S. A. Differential effects of hyperthermia on murine bone marrow normal colony-forming units and AKR and L1210 Leukemia stem cells. Cancer Research 1984; 44: 1761–1766
   PubMed Web of Science ®Google Scholar
• Goris H., Loeffler M., Bungart B., Schmitz S., Nijhof W. Hemopoiesis during thiamphenicol treatment I. Stimulation of stem cells during eradication of intermediate cell stages. Experimental Hematology 1989; 17: 957–961
   PubMed Web of Science ®Google Scholar
• Harris R. A., Hogarth P. M., Wadeson L. J., Collins P., McKenzie I. F. C., Pennington D. G. An antigenic difference between cells forming early and late haemopoietic spleen colonies (CFU-S). Nature (London) 1984; 307: 638–641
   PubMed Web of Science ®Google Scholar
• Hodgson G. S., Bradley T. R. Properties of haematopoietic stem cells surviving 5-fluorouracil treatment: evidence for a pre-CFU-S?. Nature (London) 1979; 281: 381–382
   PubMed Web of Science ®Google Scholar
• Magli M. C., Iscove N. N., Odartchenko N. Transient nature of early haematopoietic spleen colonies. Nature (London) 1982; 295: 527–529
   PubMed Web of Science ®Google Scholar
• Mivechi N. F., Li G. C. Lack of development of thermotolerance in early progenitors of murine bone marrow cells. Cancer Research 1986; 46: 198–202
   PubMed Web of Science ®Google Scholar
• Mivechi N. F., Ogilvie P. D. Enhancement of murine bone marrow ablation by combining whole body hyperthermia with total body irradiation and cyclophosphamide. International Journal of Radiation Oncology, Biology and Physics 1989; 17: 117–123
   PubMedGoogle Scholar
• Molineux G., Schofield R., Testa N. G. Development of spleen CFU-S colonies from day 8 to day 11: relationship to self-renewal capacity. Experimental Hematology 1986; 14: 710–713
   PubMed Web of Science ®Google Scholar
• Monette F. C., DeMello J. B. The relationship between stem cell seeding efficiency and position in cell cycle. Cell Tissue Kinetics 1979; 12: 161–175
   PubMedGoogle Scholar
• Moriyama Y., Narita M., Sato K., Urushiyama M., Koyama S., Hirosawa H., Kishi K., Takahashi M., Shibata A. Application of hyperthermia to the treatment of human acute leukemia: purging human leukemic progenitor cells by heat. Blood 1986; 67: 802–804
   PubMed Web of Science ®Google Scholar
• Murphy P. B., Richman C. M. Normal and malignant human myeloid progenitors differ in their sensitivity to hyperthermia. Experimental Hematology 1989; 17: 1105–1109
   PubMed Web of Science ®Google Scholar
• Nijhof W., Wierenga P. K., Goldwasser E. The regeneration of stem cells after a bone marrow depression induced by thiamphenicol. Experimental Hematology 1982; 10: 36–43
   PubMedGoogle Scholar
• Nijhof W., Wierenga P. K. Isolation of hemopoietic pluripotent stem cells from spleens of thiamphenicol-pretreated mice. Experimental Cell Research 1984; 155: 583–587
   PubMedGoogle Scholar
• Nijhof W., Wierenga P. K. Characterization of a cycling murine pluripotent stem cell population. European Journal of Cell Biology 1985; 39: 136–141
   PubMedGoogle Scholar
• Ploemacher R. E., Brons N. H. C., Leenen P. J. M. Bulk enrichment of transplantable hemopoietic stem cell subsets from lipopolysacharide-stimulated murine spleen. Experimental Hematology 1987; 15: 154–162
   PubMedGoogle Scholar
• Ploemacher R. E., Brons N. H. C. 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. Experimental Hematology 1988a; 16: 21–26
   PubMed Web of Science ®Google Scholar
• Ploemacher R. E., Brons N. H. C. In vivo proliferative and differential properties of murine bone marrow cells separated on the basis of rhodamine-123 retention. Experimental Hematology 1988b; 16: 903–907
   PubMedGoogle Scholar
• Priestly G. V., Wolf N. S. A technique for the daily examination of spleen colonies in mice. Experimental Hematology 1985; 13: 733–735
   PubMed Web of Science ®Google Scholar
• Robins H. I., Steeves R. A., Clark A. W., Martin P. A., Miller K., Dennis W. H. Differential sensitivity of AKR murine leukemia and normal bone marrow cells to hyperthermia. Cancer Research 1983; 43: 4951–4955
   PubMedGoogle Scholar
• Robins H. I., Steeves R. A., Schmitt C. L., Peterson C., Martin P. A. A hyperthermia study of differential sensitivity and thermotolerance in AKR murine leukemia and normal bone marrow cells. International Journal of Radiation Oncology, Biology and Physics 1988; 14: 979–982
   PubMed Web of Science ®Google Scholar
• Russell E. S., Bernstein E. Blood and blood formation. Biology of the Laboratory Mouse, E. L. Green. New York: McGraw-Hill, London 1966; 351–372
   Google Scholar
• Schneider E., Pollard H., Lepault F., Guy-Grand D., Minkowski M., Dy M. Histamine-producing colony-stimulating activity: interleukin 3 and granulocyte-macrophage colony stimulating factor induce de novo synthesis of histidine decarboxylase in hemopoietic progenitor cells. Journal of Immunology 1987; 139: 3710–3717
   PubMedGoogle Scholar
• Shibagaki T., Inoue T., Kubota N., Kanisawa M. Fraction of pluripotent hemopoietic stem cells in DNA synthesis varies with generation age. Experimental Hematology 1986; 14: 794–797
   PubMed Web of Science ®Google Scholar
• Spooncer E., Lord B. I., Dexter T. M. Defective ability to self-renew in vitro of highly purified primitive haemopoietic cells. Nature (London) 1985; 316: 62–64
   PubMedGoogle Scholar
• Symonds R. P., Wheldon T. E., Clarke B., Bailey G. A comparison of the response to hyperthermia of murine haemopoietic stem cells (CFU-S) and L1210 leukaemia cells: enhanced killing of leukaemic cells in presence of normal marrow cells. British Journal of Cancer 1981; 44: 682–691
   PubMed Web of Science ®Google Scholar
• Till J. E., McCulloch E. A. A direct measurement of the radiation sensitivity of normal mouse bone marrow cells. Radiation Research 1961; 14: 213–222
   PubMed Web of Science ®Google Scholar
• VanZant G., Flentje D., Flentje M. The effect of hyperthermia on hemopoietic progenitor cells of the mouse. Radiation Research 1983; 95: 142–149
   PubMedGoogle Scholar
• Visser I. W. M., Bauman J. G. J., Mulder A. H., Eliason J. F., De Leeuw A. M. Isolation of murine pluripotent hemopoietic stem cells. Journal of Experimental Medicine 1984; 50: 1576–1590
   Google Scholar
• Visser J. W. M., VanBekkum D. W. Purification of pluripotent hemopoietic stem cells: past and present. Experimental Hematology 1990; 18: 248–257
   PubMedGoogle Scholar
• Wang S. B., Hendry J. H., Testa N. G. Thermal sensitivity of haemopoietic and stromal progenitor cells in different proliferative states. British Journal of Cancer 1985; 52: 51–54
   PubMed Web of Science ®Google Scholar
• Wierenga P. K., Konings A. W. T. Effect of a hyperthermic treatment on the pluripotent haemopoietic stem cell in normal and anaemic mice. International Journal of Hyperthermia 1990; 6: 793–800
   PubMed Web of Science ®Google Scholar