Evidence map›Paper›PMID 26618801›Full record

ArticlePloS one2015

γ-H2AX Kinetic Profile in Mouse Lymphocytes Exposed to the Internal Emitters Cesium-137 and Strontium-90.

Helen C Turner, Igor Shuryak, Waylon Weber, Melanie Doyle-Eisele, Dunstana Melo, Raymond Guilmette, Sally A Amundson, David J Brenner

Abstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

  1. Article
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  5. Article
  6. VADER: a variable dose-rate externalScientific reports · 2020
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. THE DECADE OF THE RABiT (2005-15).Radiation protection dosimetry · 2016
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Helen C TurnerCenter for Radiological Research, Columbia University Medical Center, New York, New York, United States of America.
Igor ShuryakCenter for Radiological Research, Columbia University Medical Center, New York, New York, United States of America.
Waylon WeberLovelace Respiratory Research Institute, Albuquerque, New Mexico, United States of America.
Melanie Doyle-EiseleLovelace Respiratory Research Institute, Albuquerque, New Mexico, United States of America.
Dunstana MeloLovelace Respiratory Research Institute, Albuquerque, New Mexico, United States of America.
Raymond GuilmetteLovelace Respiratory Research Institute, Albuquerque, New Mexico, United States of America.
Sally A AmundsonCenter for Radiological Research, Columbia University Medical Center, New York, New York, United States of America.
David J BrennerCenter for Radiological Research, Columbia University Medical Center, New York, New York, United States of America.

Funding

Sample Engineering CoreU19AI067773 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI FORNACE, ALBERT J · 2005 to 2024
$105.4M
NIAID NIH HHS U19 AI067773NIAID NIH HHS U19AI067773
6 · The paper itself

Abstract

In the event of a dirty bomb scenario or an industrial nuclear accident, a significant dose of volatile radionuclides such as 137Cs and 90Sr may be dispersed into the atmosphere as a component of fallout and inhaled or ingested by hundreds and thousands of people. To study the effects of prolonged exposure to ingested radionuclides, we have performed long-term (30 day) internal-emitter mouse irradiations using soluble-injected 137CsCl and 90SrCl2 radioisotopes. The effect of ionizing radiation on the induction and repair of DNA double strand breaks (DSBs) in peripheral mouse lymphocytes in vivo was determined using the γ-H2AX biodosimetry marker. Using a serial sacrifice experimental design, whole-body radiation absorbed doses for 137Cs (0 to 10 Gy) and 90Sr (0 to 49 Gy) were delivered over 30 days following exposure to each radionuclide. The committed absorbed doses of the two internal emitters as a function of time post exposure were calculated based on their retention parameters and their derived dose coefficients for each specific sacrifice time. In order to measure the kinetic profile for γ-H2AX, peripheral blood samples were drawn at 5 specific timed dose points over the 30-day study period and the total γ-H2AX nuclear fluorescence per lymphocyte was determined using image analysis software. A key finding was that a significant γ-H2AX signal was observed in vivo several weeks after a single radionuclide exposure. A mechanistically-motivated model was used to analyze the temporal kinetics of γ-H2AX fluorescence. Exposure to either radionuclide showed two peaks of γ-H2AX: one within the first week, which may represent the death of mature, differentiated lymphocytes, and the second at approximately three weeks, which may represent the production of new lymphocytes from damaged progenitor cells. The complexity of the observed responses to internal irradiation is likely caused by the interplay between continual production and repair of DNA damage, cell cycle effects and apoptosis.

Indexed as

AnimalsApoptosisCell CycleCesium RadioisotopesDNA Breaks, Double-StrandedDNA RepairDose-Response Relationship, RadiationHistonesKineticsLymphocytesMiceStrontium RadioisotopesWhole-Body IrradiationCesium RadioisotopesH2AX protein, humanHistonesStrontium Radioisotopes

Identifiers

PMID26618801
PMCPMC4664397

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.