Comparison of signaling profiles in the low dose range following low and high LET radiation.


Journal

Life sciences in space research
ISSN: 2214-5532
Titre abrégé: Life Sci Space Res (Amst)
Pays: Netherlands
ID NLM: 101632373

Informations de publication

Date de publication:
May 2020
Historique:
received: 22 12 2019
revised: 10 02 2020
accepted: 13 02 2020
entrez: 17 5 2020
pubmed: 18 5 2020
medline: 20 1 2021
Statut: ppublish

Résumé

During space travel astronauts will be exposed to a very low, mixed field of radiation containing different high LET particles of varying energies, over an extended period. Thus, defining how human cells respond to these complex low dose exposures is important in ascertaining risk. In the current study, we have chosen to investigate how low doses of three different ion's at various energies uniquely change the kinetics of three different phospho-proteins. A normal hTERT immortalized fibroblast cell line, 82-6, was exposed to a range of lower doses (0.05-0.5 Gy) of radiation of different qualities and energies (Si 1000 MeV/u, Si 300 MeV/u, Si 173 MeV/u, Si 93 MeV/u, Fe 1000 MeV/u, Fe 600 MeV/u, Fe 300 MeV/u, Ti 300 MeV/u, Ti 326 MeV/u, Ti 386 MeV/u), covering a wide span of LET's. Exposed samples were analyzed for the average intensity of signal as a fold over the geometric mean level of the sham controls. Three phospho-proteins known to localize to DNA DSBs following radiation (γH2AX, pATF2, pSMC1) were studied. The kinetics of their response was quantified by flow cytometery at 2 and 24 h post exposure. These studies reveal unique kinetic patterns based on the ion, energy, fluence and time following exposure. In addition, γH2AX phosphorylation patterns are uniquely different from phospho-proteins known to be primarily phosphorylated by ATM. This latter finding suggests that the activating kinase(s), or the phosphatases deactivating these proteins, exhibit differences in their response to various radiation qualities and/ or doses of exposure. Further studies will be needed to better define what the differing kinetics for the kinases activated by the unique radiation qualities plays in the biological effectiveness of the particle.

Identifiants

pubmed: 32414491
pii: S2214-5524(20)30010-9
doi: 10.1016/j.lssr.2020.02.002
pii:
doi:

Substances chimiques

Phosphoproteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

28-41

Informations de copyright

Copyright © 2020 The Committee on Space Research (COSPAR). Published by Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest None.

Auteurs

Deepa M Sridharan (DM)

Lawrence Berkeley National Laboratory, Life Sciences Division, Berkeley, CA 94710, United States.

Lung-Chang Chien (LC)

Department of Environmental and Occupational Health, University of Nevada, Las Vegas, NV, 89154, United States.

Francis A Cucinotta (FA)

Health Physics and Diagnostic Sciences, University of Nevada, Las Vegas, NV 89154, United States.

Janice M Pluth (JM)

Health Physics and Diagnostic Sciences, University of Nevada, Las Vegas, NV 89154, United States. Electronic address: Janice.pluth@unlv.edu.

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