Evidence map›Paper›PMID 32932286›Full record

ArticleHealth physics2020

Development of a Model of the Acute and Delayed Effects of High Dose Radiation Exposure in Jackson Diversity Outbred Mice; Comparison to Inbred C57BL/6 Mice.

Andrea M Patterson, P Artur Plett, Hui Lin Chua, Carol H Sampson, Alexa Fisher, Hailin Feng, Joseph L Unthank, Steven J Miller, Barry P Katz, Thomas J MacVittie and 1 more

Abstract readComparative Study
In one paragraph

Article in Health physics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Fifteen years of the Diversity Outbred mouse model: a review.Mammalian genome : official journal of the International Mammalian Genome Society · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Sex differences in radiation research.International journal of radiation biology · 2024
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Biomarkers to Predict Lethal Radiation Injury to the Rat Lung.International journal of molecular sciences · 2023
    Article
  12. Establishing a Murine Model of the Hematopoietic Acute Radiation Syndrome.Methods in molecular biology (Clifton, N.J.) · 2023
    Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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

11 authors.

Andrea M PattersonDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN.
P Artur PlettDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN.
Hui Lin ChuaDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN.
Carol H SampsonDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN.
Alexa FisherDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN.
Hailin FengDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN.
Joseph L UnthankDepartment of Surgery, Indiana University School of Medicine, Indianapolis, IN.
Steven J MillerDepartment of Surgery, Indiana University School of Medicine, Indianapolis, IN.
Barry P KatzDepartment of Biostatistics, Indiana University School of Medicine, Indianapolis, IN.
Thomas J MacVittieDepartment of Radiation Oncology, University of Maryland School of Medicine, Baltimore, MD.
Christie M OrschellDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN.

Funding

Age-Related Differences in Response to Radiation and Medical CountermeasuresUH3AI128894 · NIAID · INDIANA UNIVERSITY INDIANAPOLIS · PI ORSCHELL, CHRISTIE M, PELUS, LOUIS M · 2018 to 2020
$450k
NIAID NIH HHS HHSN272201000046CNIAID NIH HHS UH3 AI128894
6 · The paper itself

Abstract

Development of medical countermeasures against radiation relies on robust animal models for efficacy testing. Mouse models have advantages over larger species due to economics, ease of conducting aging studies, existence of historical databases, and research tools allowing for sophisticated mechanistic studies. However, the radiation dose-response relationship of inbred strains is inherently steep and sensitive to experimental variables, and inbred models have been criticized for lacking genetic diversity. Jackson Diversity Outbred (JDO) mice are the most genetically diverse strain available, developed by the Collaborative Cross Consortium using eight founder strains, and may represent a more accurate model of humans than inbred strains. Herein, models of the Hematopoietic-Acute Radiation Syndrome and the Delayed Effects of Acute Radiation Exposure were developed in JDO mice and compared to inbred C57BL/6. The dose response relationship curve in JDO mice mirrored the more shallow curves of primates and humans, characteristic of genetic diversity. JDO mice were more radioresistant than C57BL/6 and differed in sensitivity to antibiotic countermeasures. The model was validated with pegylated-G-CSF, which provided significantly enhanced 30-d survival and accelerated blood recovery. Long-term JDO survivors exhibited increased recovery of blood cells and functional bone marrow hematopoietic progenitors compared to C57BL/6. While JDO hematopoietic stem cells declined more in number, they maintained a greater degree of quiescence compared to C57BL/6, which is essential for maintaining function. These JDO radiation models offer many of the advantages of small animals with the genetic diversity of large animals, providing an attractive alternative to currently available radiation animal models.

Indexed as

Acute Radiation SyndromeAnimalsBone MarrowCollaborative Cross MiceDisease Models, AnimalHematopoietic Stem CellsMaleMiceMice, Inbred C57BLRadiation DosageRadiation ExposureRadiation Injuries, Experimental

Identifiers

PMID32932286
PMCPMC9374540

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Registered trials

None linked

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.