Literature DB >> 21988573

Effects of very low fluences of high-energy protons or iron ions on irradiated and bystander cells.

H Yang1, N Magpayo, A Rusek, I-H Chiang, M Sivertz, K D Held.   

Abstract

In space, astronauts are exposed to radiation fields consisting of energetic protons and high atomic number, high-energy (HZE) particles at very low dose rates or fluences. Under these conditions, it is likely that, in addition to cells in an astronaut's body being traversed by ionizing radiation particles, unirradiated cells can also receive intercellular bystander signals from irradiated cells. Thus this study was designed to determine the dependence of DNA damage induction on dose at very low fluences of charged particles. Novel techniques to quantify particle fluence have been developed at the NASA Space Radiation Biology Laboratory (NSRL) at Brookhaven National Laboratory (BNL). The approach uses a large ionization chamber to visualize the radiation beam coupled with a scintillation counter to measure fluence. This development has allowed us to irradiate cells with 1 GeV/nucleon protons and iron ions at particle fluences as low as 200 particles/cm(2) and quantify biological responses. Our results show an increased fraction of cells with DNA damage in both the irradiated population and bystander cells sharing medium with irradiated cells after low fluences. The fraction of cells with damage, manifest as micronucleus formation and 53BP1 focus induction, is about 2-fold higher than background at doses as low as ∼0.47 mGy iron ions (∼0.02 iron ions/cell) or ∼70 μGy protons (∼2 protons/cell). In the irradiated population, irrespective of radiation type, the fraction of damaged cells is constant from the lowest damaging fluence to about 1 cGy, above which the fraction of damaged cells increases with dose. In the bystander population, the level of damage is the same as in the irradiated population up to 1 cGy, but it does not increase above that plateau level with increasing dose. The data suggest that at fluences of high-energy protons or iron ions less than about 5 cGy, the response in irradiated cell populations may be dominated by the bystander response.

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Year:  2011        PMID: 21988573     DOI: 10.1667/rr2674.1

Source DB:  PubMed          Journal:  Radiat Res        ISSN: 0033-7587            Impact factor:   2.841


  13 in total

1.  Investigation of the bystander effect in CHO-K1 cells.

Authors:  Urszula Kaźmierczak; Dariusz Banaś; Janusz Braziewicz; Iwona Buraczewska; Joanna Czub; Marian Jaskóła; Łukasz Kaźmierczak; Andrzej Korman; Marcin Kruszewski; Anna Lankoff; Halina Lisowska; Marta Nesteruk; Zygmunt Szefliński; Maria Wojewódzka
Journal:  Rep Pract Oncol Radiother       Date:  2014-05-19

2.  Functional consequences of radiation-induced oxidative stress in cultured neural stem cells and the brain exposed to charged particle irradiation.

Authors:  Bertrand P Tseng; Erich Giedzinski; Atefeh Izadi; Tatiana Suarez; Mary L Lan; Katherine K Tran; Munjal M Acharya; Gregory A Nelson; Jacob Raber; Vipan K Parihar; Charles L Limoli
Journal:  Antioxid Redox Signal       Date:  2013-08-12       Impact factor: 8.401

Review 3.  Evaluating biomarkers to model cancer risk post cosmic ray exposure.

Authors:  Deepa M Sridharan; Aroumougame Asaithamby; Steve R Blattnig; Sylvain V Costes; Paul W Doetsch; William S Dynan; Philip Hahnfeldt; Lynn Hlatky; Yared Kidane; Amy Kronenberg; Mamta D Naidu; Leif E Peterson; Ianik Plante; Artem L Ponomarev; Janapriya Saha; Antoine M Snijders; Kalayarasan Srinivasan; Jonathan Tang; Erica Werner; Janice M Pluth
Journal:  Life Sci Space Res (Amst)       Date:  2016-05-21

4.  Cellular Response to Proton Irradiation: A Simulation Study with TOPAS-nBio.

Authors:  Hongyu Zhu; Aimee L McNamara; Stephen J McMahon; Jose Ramos-Mendez; Nicholas T Henthorn; Bruce Faddegon; Kathryn D Held; Joseph Perl; Junli Li; Harald Paganetti; Jan Schuemann
Journal:  Radiat Res       Date:  2020-07-08       Impact factor: 2.841

5.  Quantification of radiation-induced DNA double strand break repair foci to evaluate and predict biological responses to ionizing radiation.

Authors:  Sébastien Penninckx; Eloise Pariset; Egle Cekanaviciute; Sylvain V Costes
Journal:  NAR Cancer       Date:  2021-12-22

6.  Low-dose energetic protons induce adaptive and bystander effects that protect human cells against DNA damage caused by a subsequent exposure to energetic iron ions.

Authors:  Manuela Buonanno; Sonia M De Toledo; Roger W Howell; Edouard I Azzam
Journal:  J Radiat Res       Date:  2015-03-23       Impact factor: 2.724

7.  Issues for Simulation of Galactic Cosmic Ray Exposures for Radiobiological Research at Ground-Based Accelerators.

Authors:  Myung-Hee Y Kim; Adam Rusek; Francis A Cucinotta
Journal:  Front Oncol       Date:  2015-06-04       Impact factor: 6.244

8.  Radiation quality-dependence of bystander effect in unirradiated fibroblasts is associated with TGF-β1-Smad2 pathway and miR-21 in irradiated keratinocytes.

Authors:  Xiaoming Yin; Wenqian Tian; Longxiao Wang; Jingdong Wang; Shuyu Zhang; Jianping Cao; Hongying Yang
Journal:  Sci Rep       Date:  2015-06-16       Impact factor: 4.379

9.  Characterizing low dose and dose rate effects in rodent and human neural stem cells exposed to proton and gamma irradiation.

Authors:  Bertrand P Tseng; Mary L Lan; Katherine K Tran; Munjal M Acharya; Erich Giedzinski; Charles L Limoli
Journal:  Redox Biol       Date:  2013-01-19       Impact factor: 11.799

10.  Relative Biological Effectiveness of HZE Particles for Chromosomal Exchanges and Other Surrogate Cancer Risk Endpoints.

Authors:  Eliedonna Cacao; Megumi Hada; Premkumar B Saganti; Kerry A George; Francis A Cucinotta
Journal:  PLoS One       Date:  2016-04-25       Impact factor: 3.240

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