Effect of Syngeneic Bone Marrow and Thymus Cell Transplantation to ⁹⁰Sr Irradiated Mice

References

• Barnes D. W. H., Bungay G. T., Mole R. H. Delayed mortality of midlethal exposures to whole‐body irradiation and its modification by treatment with syngeneic lymph‐node or bone‐marrow cells. Int. J. radiat. Biol. 1966; 11: 409
   Google Scholar
• Cole L. J., Obermaeyer J. G., Bond V. P. Recovery from acute radiation injury in mice following administration of rat bone marrow. J. Nat. Cancer Inst. 1955; 16: 1
   PubMedGoogle Scholar
• Congdon C. C., Makinodan T., Genogozian N. Effect of injection of rat bone marrow on reticular tissues of mice exposed to X radiation in the midlethal dose range. J. nat. Cancer Inst. 1957; 18: 603
   PubMedGoogle Scholar
• Cosgrove G. E., Upton A. C., Congdon C. C., Doherty D. G., Christenberry K. W., Gosslee D. G. Late somatic effects of x‐radiation in mice treated with AET and isologous bone marrow. Radiat. Res. 1964; 21: 550
   PubMedGoogle Scholar
• Covelli V., Metalli P., Briganti G., Bassini B., Silini G. Late somatic effects in syngeneric radiation chemaeras. II. Mortality and rate of specific diseases. Int. J. radiat. Biol. 1974; 26: 1
   Google Scholar
• Duplan J. F., Rechtikov V. P., , Kosinetz G, et al. Effet de la moelle osseuse homologue provenant de donneurs tolérante sur la survie de souris irradiées. C. R. Soc. Biol. 1962; 156: 1773
   Google Scholar
• Haller O., Wigzell H. Suppression of natural killer cell activity with radioactive strontium. Effector cells are marrow‐dependent. J. Immunol. 1977; 118: 1503
   PubMed Web of Science ®Google Scholar
• Jacobson L. O. The haematological effects of ionizing radiation. Biology, A. Hollaender. McGraw‐Hill, New York, Toronto, London 1954; Vol. 1
   Google Scholar
• Jacobson L. O., Simmons E. L., Marks E. K., Gaston E. O., Robson M. J. Further studies on recovery from radiation injury. J. Lab. Clin. Med 1951; 37: 683
   PubMed Web of Science ®Google Scholar
• Järplid B. Radiation induced asymmetry and lymphoma of thymus in mice. Acta radiol. 1968, Suppl. No. 279
   Google Scholar
• Järplid B. Radiostrontium induced early changes in the haematopoietic tissues. With special reference to the thymus in mice. Acta radiol. Ther. Phys. Biol. 1973; 12: 145
   PubMedGoogle Scholar
• Järplid B. Combined effect of roentgen irradiation and radiostrontium on the haematopoietic tissues and the development of lymphoma in mice. Acta radiol. Ther. Phys. Biol. 1974; 13: 217
   PubMedGoogle Scholar
• Kaplan H. S., Brown M. B. Protection against radiation‐induced lymphoma development by shielding and partial‐body irradiation of mice. Cancer Res. 1952; 12: 44
   PubMed Web of Science ®Google Scholar
• Kaplan H. S., Brown M. B., Paull J. Influence of bone marrow injections on involution and neoplasia of mouse thymus after systemic irradiation. J. nat. Cancer Inst. 1953; 14: 303
   PubMed Web of Science ®Google Scholar
• Kiessling R., Wigzell H. An analysis of the murine NK‐cell as to structure, function and biological relevance. Immunol. Rev. 1979; 44: 165
   PubMed Web of Science ®Google Scholar
• McCulloch E. A., Till J. E. Proliferation of haematopoietic colony forming cells transplanted into irradiated mice. Radiat. Res. 1964; 22: 383
   PubMed Web of Science ®Google Scholar
• Metalli P., Silini G., Covelli V., Bassini B. Late somatic effects in syngeneic radiation chimaeras. III. Observations on animals repopulated with irradiated marrow. Int. J. radiat. Biol. 1976; 29: 413
   Google Scholar
• Nilsson A. Effect of radiostrontium on the blood and haematopoietic tissues of mice. Acta vet. scand. 1962; 3: 103
   Google Scholar
• Nilsson A. Pathologic effects of different doses of radiostrontium in mice. Changes of the haematopoietic system. Acta radiol. Ther. Phys. Biol. 1970; 9: 528
   PubMed Web of Science ®Google Scholar
• Nilsson A. Pathologic effects of different doses of radiostrontium in mice. Dose effect relationship in 90Sr‐induced tumours. Acta radiol. Ther. Phys. Biol. 1970; 9: 155
   PubMedGoogle Scholar
• Nilsson A. Pathologic effects of different doses of radiostrontium in mice. Development and incidence of leukemia. Acta radiol. Ther. Phys. Biol. 1971; 10: 115
   PubMed Web of Science ®Google Scholar
• Nilsson A., Broomé‐Karlsson A. The pathology of americium 241. Acta radiol. Ther. Phys. Biol. 1976; 15: 49
   PubMed Web of Science ®Google Scholar
• Nilsson A., Ullberg S. Uptake and retention of strontium 90 in mouse tissues studied by whole animal autoradiography and impulse counting. I. Acta radiol. 1962; 58: 81
   PubMed Web of Science ®Google Scholar
• Sprent J., Basten A. Circulating T and B lymphocytes of the mouse II. Lifespan. Cell Immunol. 1973; 7: 40
   PubMedGoogle Scholar
• Till J. E., McCulloch E. A. A direct measurement of the radiation sensitivity of normal mouse bone marrow cells. Radiat. Res. 1961; 14: 213
   PubMed Web of Science ®Google Scholar
• Unsgaard B. Optimal tissue for marrow injection in mice after total body irradiation. Acta radiol. 1961; 56: 296
   PubMed Web of Science ®Google Scholar
• Urso P., Congdon C. C. The effect of the amount of isologous bone marrow injected on the recovery of haematopoietic organs, survival and body weight after lethal irradiation injury in mice. Blood 1957; 12: 251
   PubMed Web of Science ®Google Scholar
• Wallis V., Davies A. J. S., Koller P. C. Inhibition of radiation‐induced leukaemia by the injection of haematopoietic tissue. A study of chimoaerism. Nature 1966; 210: 500
   PubMed Web of Science ®Google Scholar
• Zatz M. M., Lance E. M. The distribution of chromium 51‐labelled lymphoid cells in mouse. A survey of anatomical compartments. Cell Immunol. 1970; I: 3
   Google Scholar