TY - JOUR
T1 - The impact of mouse strain on iron ion radio-immune response of leukocyte populations
AU - Pecaut, Michael J.
AU - Gridley, Daila S.
N1 - Funding Information:
The authors thank Gregory A. Nelson, PhD, Radha Dutta-Roy, Anna L. Smith, Tamako A. Jones, Melba L. Andres, Glen M. Miller, Dong Won Kim, Judy Folz-Holbeck, Lora Benzatyan, Mauricio DosSantos, and Maritess G. Asumen for valuable technical assistance. In addition, the support of Marcelo Vazquez, PhD, Mary Ann Kershaw, Katheryn Conkling, and the AGS support staff at BNL, and the physics group from the Lawrence Berkeley Laboratory are greatly appreciated. This study was supported in part by the National Aeronautics and Space Administration (NASA NCC9-79), and the Department of Radiation Medicine of the Loma Linda University Medical Center.
PY - 2010/5
Y1 - 2010/5
N2 - Purpose:Exposure to various forms of radiation, including iron ions that have an exceptionally high biological effectiveness, is an inevitable consequence of spaceflight. However, genetic background can significantly influence the response to radiation and hence also the overall health of crewmembers. The major goal of this study was to compare leukocyte population responses in two strains of mice that differ in susceptibility to radiation: C57BL/6 (resistant) and CBA/Ca (susceptible). Materials and methods:The mice were whole-body irradiated with 0, 50, 200, or 300 cGy 56Fe 26 (1 GeV) at ∼1 Gy/min and euthanised on days 4 and 30 thereafter for analyses. Analyses included body and organ masses (spleen, liver, thymus, lungs), distribution of leukocyte populations in blood and spleen, red blood cell and platelet characteristics, expression of surface molecules (CD11b, CD54), and spontaneous and mitogen-induced blastogenesis. Results:There were main effects of Dose and Dose×Day interactions on virtually all quantified parameters in both strains of mice. In contrast, there were relatively few Dose×Strain and three-way interactions. Strain-related interactions involved changes in circulating phagocytic populations, erythrocytes, and liver mass. Conclusion:The data demonstrate that genetic background can modify certain immune-related parameters after exposure to heavy particle radiation. The possible implications of these findings are discussed. © 2010 Informa UK Ltd.
AB - Purpose:Exposure to various forms of radiation, including iron ions that have an exceptionally high biological effectiveness, is an inevitable consequence of spaceflight. However, genetic background can significantly influence the response to radiation and hence also the overall health of crewmembers. The major goal of this study was to compare leukocyte population responses in two strains of mice that differ in susceptibility to radiation: C57BL/6 (resistant) and CBA/Ca (susceptible). Materials and methods:The mice were whole-body irradiated with 0, 50, 200, or 300 cGy 56Fe 26 (1 GeV) at ∼1 Gy/min and euthanised on days 4 and 30 thereafter for analyses. Analyses included body and organ masses (spleen, liver, thymus, lungs), distribution of leukocyte populations in blood and spleen, red blood cell and platelet characteristics, expression of surface molecules (CD11b, CD54), and spontaneous and mitogen-induced blastogenesis. Results:There were main effects of Dose and Dose×Day interactions on virtually all quantified parameters in both strains of mice. In contrast, there were relatively few Dose×Strain and three-way interactions. Strain-related interactions involved changes in circulating phagocytic populations, erythrocytes, and liver mass. Conclusion:The data demonstrate that genetic background can modify certain immune-related parameters after exposure to heavy particle radiation. The possible implications of these findings are discussed. © 2010 Informa UK Ltd.
KW - Heavy particle radiation
KW - High-LET radiation
KW - Immune system
KW - Liver
KW - Radiosensitivity
KW - Blood Platelets/radiation effects
KW - Species Specificity
KW - Radiation Tolerance
KW - Leukocytes/cytology
KW - Organ Size/radiation effects
KW - Liver/radiation effects
KW - Phagocytes/cytology
KW - Time Factors
KW - Immune System Phenomena/immunology
KW - Mice, Inbred CBA
KW - Organ Specificity/radiation effects
KW - Lymphocyte Activation/radiation effects
KW - Mice, Inbred C57BL
KW - Whole-Body Irradiation/adverse effects
KW - Environmental Exposure
KW - Animals
KW - Body Weight/radiation effects
KW - Antigens, CD/radiation effects
KW - Mice
KW - Dose-Response Relationship, Radiation
KW - Iron Radioisotopes/toxicity
UR - https://www.scopus.com/pages/publications/77951270171
UR - https://www.scopus.com/pages/publications/77951270171#tab=citedBy
UR - https://www.mendeley.com/catalogue/b65000fd-722b-3d98-8557-c753ca2f2302/
U2 - 10.3109/09553000903567995
DO - 10.3109/09553000903567995
M3 - Article
C2 - 20397846
SN - 0955-3002
VL - 86
SP - 409
EP - 419
JO - International Journal of Radiation Biology
JF - International Journal of Radiation Biology
IS - 5
ER -