Pre-treatment with rapamycin protects hematopoiesis against radiation injury

被引:0
作者
Wang, Z. [1 ]
Fang, Y. [1 ]
Nie, M. [1 ]
Yuan, N. [1 ]
Wang, J. [1 ]
Zhang, S. [1 ]
机构
[1] Soochow Univ, Hematol Ctr,Sch Med, Collaborat Innovat Ctr Hematol,Cyrus Tang Med Ins, Jiangsu Key Lab Stem Cell Res,Jiangsu Inst Hemato, Suzhou 215123, Peoples R China
来源
INTERNATIONAL JOURNAL OF RADIATION RESEARCH | 2018年 / 16卷 / 01期
基金
中国国家自然科学基金;
关键词
Rapamycin; hematopoiesis; ionization radiation; radiation injury and protection; INDUCED GENOMIC INSTABILITY; DOUBLE-STRAND BREAKS; DNA-DAMAGE RESPONSE; STEM-CELLS; IONIZING-RADIATION; MAMMALIAN TARGET; BONE-MARROW; HOMOLOGOUS RECOMBINATION; OXIDATIVE STRESS; REPAIR;
D O I
10.18869/acadpub.ijrr.16.1.65
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Background: Protection of hematopoietic system has become a primary goal in the development of novel medical countermeasures against ionization radiation and radiotherapy. This study was to explore the role of rapamycin in normal tissues against radiation. Materials and Methods: Mice were pretreated with rapamycin by i.p. every other day for five times before 5 Gy or 8.5 Gy gamma-ray whole body irradiation. Blood cell counts, HE staining of bone marrow and liver, bone marrow transplantation, CFU of spleen were used to measure the damage of hematopoiesis and extramedullary hemopoietic organs. Regular karyotype analysis and expression of gamma-H2AX (by flow cytometry and western blot) were used to measure DNA damage. Rad 50 and DNA Lig 4 expression by western blot were to see the DNA repair ability. Results: The decrease of red blood cells and platelet induced by radiation were alleviated by pretreatment with rapamycin (d 7,15, p<0.01), and the long-term restoration of white blood cells, lymphocytes and bone marrow were enhanced in rapamycin pretreatment group (d 30,40,70, p<0.05). The transplantation experiment also indicates that the long-term reconstitution in lethally irradiated recipient mice was improved in rapamycin group (p<0.05). The hepatocellular injury by radiation was also reduced and the colony formation numbers of spleen after irradiation was improved in rapamycin group (p<0.05). Karyotype analysis indicates that rapamycin protected bone marrow cells from chromosome mutation. Furthermore, expression of DNA repair proteins Rad 50 and DNA Lig 4 was enhanced and DNA damage marker gamma-H2AX was reduced in mice exposed to radiation by rapamycin pretreatment. Conclusion: Rapamycin pretreatment mitigates hematopoietic system from radiation injury in both bone marrow and extramedullary hematopoietic organs by improving genomic stability and increasing survival of hematopoietic stem and progenitor cells (HSPCs).
引用
收藏
页码:65 / 74
页数:10
相关论文
共 33 条
[1]   Quantitative Nuclear Proteomics Identifies mTOR Regulation of DNA Damage Response [J].
Bandhakavi, Sricharan ;
Kim, Young-Mi ;
Ro, Seung-Hyun ;
Xie, Hongwei ;
Onsongo, Getiria ;
Jun, Chang-Bong ;
Kim, Do-Hyung ;
Griffin, Timothy J. .
MOLECULAR & CELLULAR PROTEOMICS, 2010, 9 (02) :403-414
[2]  
Boroujeni Mandana Beigi, 2009, Iranian Biomedical Journal, V13, P87
[3]   Homologous recombination is necessary for normal lymphocyte development [J].
Caddle, Lura B. ;
Hasham, Muneer G. ;
Schott, William H. ;
Shirley, Bobbi-Jo ;
Mills, Kevin D. .
MOLECULAR AND CELLULAR BIOLOGY, 2008, 28 (07) :2295-2303
[4]   Inhibition of mammalian target of rapamycin or apoptotic pathway induces autophagy and radiosensitizes PTEN null prostate cancer cells [J].
Cao, Carolyn ;
Subhawong, Ty ;
Albert, Jeffrey M. ;
Kim, Kwang Woon ;
Geng, Ling ;
Sekhar, Konjeti R. ;
Gi, Young Jin ;
Lu, Bo .
CANCER RESEARCH, 2006, 66 (20) :10040-10047
[5]   TSC-mTOR maintains quiescence and function of hematopoietic stem cells by repressing mitochondrial biogenesis and reactive oxygen species [J].
Chen, Chong ;
Liu, Yu ;
Liu, Runhua ;
Ikenoue, Tsuneo ;
Guan, Kun-Liang ;
Liu, Yang ;
Zheng, Pan .
JOURNAL OF EXPERIMENTAL MEDICINE, 2008, 205 (10) :2397-2408
[6]   Short-Term and Long-Term Health Risks of Nuclear-Power-Plant Accidents [J].
Christodouleas, John P. ;
Forrest, Robert D. ;
Ainsley, Christopher G. ;
Tochner, Zelig ;
Hahn, Stephen M. ;
Glatstein, Eli .
NEW ENGLAND JOURNAL OF MEDICINE, 2011, 364 (24) :2334-2341
[7]   Radiation-induced genomic instability and persisting oxidative stress in primary bone marrow cultures [J].
Clutton, SM ;
Townsend, KMS ;
Walker, C ;
Ansell, JD ;
Wright, EG .
CARCINOGENESIS, 1996, 17 (08) :1633-1639
[8]   Exposure to Low-Dose Ionizing Radiation from Medical Imaging Procedures. [J].
Fazel, Reza ;
Krumholz, Harlan M. ;
Wang, Yongfei ;
Ross, Joseph S. ;
Chen, Jersey ;
Ting, Henry H. ;
Shah, Nilay D. ;
Nasir, Khurram ;
Einstein, Andrew J. ;
Nallamothu, Brahmajee K. .
NEW ENGLAND JOURNAL OF MEDICINE, 2009, 361 (09) :849-857
[9]   Focusing on Foci H2AX and the Recruitment of DNA-Damage Response Factors [J].
Fernandez-Capetillo, Oscar ;
Celeste, Arkady ;
Nussenzweig, Andre .
CELL CYCLE, 2003, 2 (05) :426-427
[10]   Autophagy Regulates Pancreatic Beta Cell Death in Response to Pdx1 Deficiency and Nutrient Deprivation [J].
Fujimoto, Kei ;
Hanson, Piia T. ;
Tran, Hung ;
Ford, Eric L. ;
Han, Zhiqiang ;
Johnson, James D. ;
Schmidt, Robert E. ;
Green, Karen G. ;
Wice, Burton M. ;
Polonsky, Kenneth S. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (40) :27664-27673