Evidence map›Paper›PMID 34075076›Full record

ArticleScientific reports2021

Immunological and hematological outcomes following protracted low dose/low dose rate ionizing radiation and simulated microgravity.

Amber M Paul, Eliah G Overbey, Willian A da Silveira, Nathaniel Szewczyk, Nina C Nishiyama, Michael J Pecaut, Sulekha Anand, Jonathan M Galazka, Xiao Wen Mao

Abstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Diallyl disulfide reduces oxidative stress to mitigate uranium tailings radiation-induced damage to the hematopoietic system.Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] · 2026
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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

9 authors.

Amber M PaulSpace Biosciences Division, NASA Ames Research Center, Moffett Field, CA, 94035, USA. amber.m.paul@nasa.gov.
Eliah G OverbeyDepartment of Genome Sciences, University of Washington, Seattle, WA, 98195, USA.
Willian A da SilveiraFaculty of Medicine, Health and Life Sciences, School of Biological Sciences, Institute for Global Food Security (IGFS), Queen's University, Belfast, BT9 5DL, Northern Ireland, UK.
Nathaniel SzewczykOhio Musculoskeletal and Neurological Institute and Department of Biomedical Sciences, Heritage College of Osteopathic Medicine, Ohio University, Athens, OH, 45701, USA.
Nina C NishiyamaDivision of Biomedical Engineering Sciences (BMES), Department of Basic Sciences, Loma Linda University, Loma Linda, CA, 92354, USA.
Michael J PecautDivision of Biomedical Engineering Sciences (BMES), Department of Basic Sciences, Loma Linda University, Loma Linda, CA, 92354, USA.
Sulekha AnandDepartment of Biological Sciences, San Jose University, San Jose, CA, 95192, USA.
Jonathan M GalazkaSpace Biosciences Division, NASA Ames Research Center, Moffett Field, CA, 94035, USA.
Xiao Wen MaoDivision of Biomedical Engineering Sciences (BMES), Department of Basic Sciences, Loma Linda University, Loma Linda, CA, 92354, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Using a ground-based model to simulate spaceflight [21-days of single-housed, hindlimb unloading (HLU) combined with continuous low-dose gamma irradiation (LDR, total dose of 0.04 Gy)], an in-depth survey of the immune and hematological systems of mice at 7-days post-exposure was performed. Collected blood was profiled with a hematology analyzer and spleens were analyzed by whole transcriptome shotgun sequencing (RNA-sequencing). The results revealed negligible differences in immune differentials. However, hematological system analyses of whole blood indicated large disparities in red blood cell differentials and morphology, suggestive of anemia. Murine Reactome networks indicated majority of spleen cells displayed differentially expressed genes (DEG) involved in signal transduction, metabolism, cell cycle, chromatin organization, and DNA repair. Although immune differentials were not changed, DEG analysis of the spleen revealed expression profiles associated with inflammation and dysregulated immune function persist to 1-week post-simulated spaceflight. Additionally, specific regulation pathways associated with human blood disease gene orthologs, such as blood pressure regulation, transforming growth factor-β receptor signaling, and B cell differentiation were noted. Collectively, this study revealed differential immune and hematological outcomes 1-week post-simulated spaceflight conditions, suggesting recovery from spaceflight is an unremitting process.

Indexed as

Hindlimb SuspensionAnimalsDose-Response Relationship, RadiationFemaleGamma RaysHematopoiesisMiceSignal Transduction

Identifiers

PMID34075076
PMCPMC8169688

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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.