Differential sensitivity to hyperthermia of mouse normal haemopoietic stem cells related to proliferation activity and organ source.

Thermosensitivity of haemopoietic stem cells was studied in relation to the organ source and the proliferative state of the cells. Heat treatment was carried out at 41, 42, 43, 44 and 45 degrees C until about 1 per cent survival was reached. Treatments at 42 degrees C and below appear to be critical in revealing thermosensitivity differences between haemopoietic stem cells, characterized by the time T(o) at a given temperature to induce a lethal event. At these temperatures, foetal liver CFU-S (about 35 per cent in S phase) were more thermosensitive than steady-state bone marrow and spleen CFU-S (less than 10 per cent in S). We consider that these thermosensitivity differences cannot be attributed exclusively to differences in proliferation rates of the CFU-S, since exponentially-proliferating marrow CFU-S (48 per cent in S) does not significantly differ in sensitivity compared with steady-state CFU-S, while regenerating spleen CFU-S does (34 per cent in S). An Arrhenius analysis of heat survival curves of the different CFU-S allowed us to estimate only one activation energy (Ea) in the inactivation process of foetal liver and regenerating spleen CFU-S, and two Ea in the case of steady-state marrow and spleen CFU-S and regenerating marrow CFU-S.

[1]  P. Nikkels,et al.  Comparative in vitro effects of cyclophosphamide derivatives on murine bone marrow-derived stromal and hemopoietic progenitor cell classes. , 1985, Cancer research.

[2]  J. Hendry,et al.  Thermal sensitivity of haemopoietic and stromal progenitor cells in different proliferative states. , 1985, British Journal of Cancer.

[3]  D. Baronciani,et al.  Effect of two cyclophosphamide derivatives on hemopoietic progenitor cells and pluripotential stem cells. , 1984, Experimental hematology.

[4]  S. Sapareto,et al.  Differential effect of hyperthermia on murine bone marrow normal colony-forming units and AKR and L1210 leukemia stem cells. , 1984, Cancer research.

[5]  A. W. Clark,et al.  Differential sensitivity of AKR murine leukemia and normal bone marrow cells to hyperthermia. , 1983, Cancer research.

[6]  T. Wheldon,et al.  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. , 1981, British Journal of Cancer.

[7]  J. R. Roti Roti,et al.  Time-temperature conversions in biological applications of hyperthermia. , 1980, Radiation research.

[8]  J. L. Roti,et al.  Comparison of two mathematical models for describing heat-induced cell killing. , 1980, Radiation research.

[9]  J. Leith,et al.  Response of 9L tumor cells to hyperthermia and X irradiation. , 1979, Radiation research.

[10]  K. Henle,et al.  Arrhenius analysis of heat survival curves from normal and thermotolerant CHO cells. , 1979, Radiation research.

[11]  W. Dewey,et al.  Cellular responses to combinations of hyperthermia and radiation. , 1977, Radiology.

[12]  L. Lajtha,et al.  MEASUREMENT OF THE KINETIC STATUS OF BONE MARROW PRECURSOR CELLS: THREE CAUTIONARY TALES , 1974, Cell and tissue kinetics.

[13]  R. Schofield A COMPARATIVE STUDY OF THE REPOPULATING POTENTIAL OF GRAFTS FROM VARIOUS HAEMOPOIETIC SOURCES: CFU REPOPULATION , 1970, Cell and tissue kinetics.

[14]  G. Silini,et al.  Studies on the haemopoietic stem cells of mouse foetal liver , 1967 .

[15]  J. Till,et al.  THE EFFECT OF DIFFERING DEMANDS FOR BLOOD CELL PRODUCTION ON DNA SYNTHESIS BY HEMOPOIETIC COLONY-FORMING CELLS OF MICE. , 1965, Blood.

[16]  J. Till,et al.  Radiation responses of hemopoietic colony-forming cells derived from different sources. , 1964 .

[17]  J. Till,et al.  A direct measurement of the radiation sensitivity of normal mouse bone marrow cells. , 1961, Radiation research.

[18]  G. Li,et al.  Lack of development of thermotolerance in early progenitors of murine bone marrow cells. , 1986, Cancer research.

[19]  A. Hirt,et al.  Purging of Bone Marrow with the B-Lymphocyte Specific Monoclonal Antibody Y29/55 and Complement: Exclusion of Antigenic Modulation , 1985 .

[20]  W. Knapp,et al.  Purging of Bone Marrow with the Monoclonal Anti Calla Antibodies VIL-A1, VIB-E3 and VIB-C5 as a Prerequisite for Autologous Bone Marrow Transplantation , 1985 .

[21]  P. Monnot,et al.  Radiosensibilité des Cellules Souches du Foie Foetal de la Souris au Cours de Leur Cycle de Multiplication , 1970 .