TY - JOUR
T1 - Effects of Obesity and Exercise on Bone Marrow Progenitor Cells after Radiation
AU - Emmons, Russell
AU - Ngu, Matthew
AU - Xu, Guanying
AU - Hernández-Saavedra, Diego
AU - Chen, Hong
AU - De Lisio, Michael
N1 - Funding Information:
Funding was graciously provided by the American Institute for Cancer Research (M. D.), the American College of Sports Medicine (M. D. and R. E.), and the National Sciences and Engineering Research Council (NSERC) of Canada (M. D.). The authors thank Dr. Leilei Yin of the Imaging Technology Group at the Beckman Institute for instruction and use of the Xardia microCT. M. D. and H. C. conceived the study design and direction. R. E., M. N., G. X., and D. H.-S. performed the experiments and analyzed the data. R. E. and M. D. wrote the manuscript. R. E., M. N., G. X., D. H.-S., H. C., and M. D. edited the manuscript and approved final submission.
Publisher Copyright:
© 2019 by the American College of Sports Medicine. Unauthorized reproduction of this article is prohibited.
PY - 2019/6/1
Y1 - 2019/6/1
N2 - Introduction The late effects of radiation therapy can have significant consequences for the health and quality of life of long-term cancer survivors. Radiation induces persistent alterations in hematopoietic stem and progenitor cells (HSPC) and the bone marrow environment; however, how relevant host factors such as obesity and exercise differentially regulate HSPC content and the bone marrow environment after radiation exposure remains unknown. The purpose of this investigation was to evaluate how the combination of obesity and exercise training modulates HSPC and their niche after sublethal radiation exposure in mice. Methods Mice fed either a control or a high-fat diet to induce obesity remained sedentary or underwent a progressive treadmill exercise program. At 13 wk of age, mice were irradiated (3 Gy) and continued their specific diets and exercise program for four more weeks. Results Exercise-trained mice had significantly higher quantities of several HSPC subpopulations and bone marrow stromal cell populations, whereas HSPC subpopulations were significantly lower in obese mice after radiation. Reactive oxygen species content was significantly decreased in HSPC with exercise training. Proteomics analysis of bone marrow supernatant revealed clustering of biologically relevant changes in exercise-trained mice. Functional evaluation of bone marrow supernatant revealed a significant increase in leukemia blast viability in obese mice but not in the exercise-trained mice (P < 0.05). Conclusion Together, these data suggest that exercise training partially restores the negative effects of obesity on HSPC and their niche after radiation exposure. As such, exercise training should be considered to mitigate the late effects of radiation therapy on the hematopoietic system for cancer survivors with or without obesity who have undergone radiation therapy.
AB - Introduction The late effects of radiation therapy can have significant consequences for the health and quality of life of long-term cancer survivors. Radiation induces persistent alterations in hematopoietic stem and progenitor cells (HSPC) and the bone marrow environment; however, how relevant host factors such as obesity and exercise differentially regulate HSPC content and the bone marrow environment after radiation exposure remains unknown. The purpose of this investigation was to evaluate how the combination of obesity and exercise training modulates HSPC and their niche after sublethal radiation exposure in mice. Methods Mice fed either a control or a high-fat diet to induce obesity remained sedentary or underwent a progressive treadmill exercise program. At 13 wk of age, mice were irradiated (3 Gy) and continued their specific diets and exercise program for four more weeks. Results Exercise-trained mice had significantly higher quantities of several HSPC subpopulations and bone marrow stromal cell populations, whereas HSPC subpopulations were significantly lower in obese mice after radiation. Reactive oxygen species content was significantly decreased in HSPC with exercise training. Proteomics analysis of bone marrow supernatant revealed clustering of biologically relevant changes in exercise-trained mice. Functional evaluation of bone marrow supernatant revealed a significant increase in leukemia blast viability in obese mice but not in the exercise-trained mice (P < 0.05). Conclusion Together, these data suggest that exercise training partially restores the negative effects of obesity on HSPC and their niche after radiation exposure. As such, exercise training should be considered to mitigate the late effects of radiation therapy on the hematopoietic system for cancer survivors with or without obesity who have undergone radiation therapy.
KW - INFLAMMATION
KW - LEUKEMIA
KW - MARROW ADIPOSE TISSUE
KW - MESENCHYMAL STEM CELLS
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U2 - 10.1249/MSS.0000000000001894
DO - 10.1249/MSS.0000000000001894
M3 - Article
C2 - 30640286
AN - SCOPUS:85065084714
SN - 0195-9131
VL - 51
SP - 1126
EP - 1136
JO - Medicine and Science in Sports and Exercise
JF - Medicine and Science in Sports and Exercise
IS - 6
ER -