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Dose and Dose-Rate Effects in a Mouse Model of Internal Exposure to 137Cs. Part 1: Global Transcriptomic Responses in
Shanaz A Ghandhi1, Chao Sima2, Waylon M Weber3
1Columbia University Irving Medical Center, New York, New York 10032.
Radiation Research
|September 15, 2020
Summary
Internal cesium-137 chloride (137CsCl) exposure in mice revealed dose-rate-dependent gene expression changes in blood cells. This study characterizes the biological impact of internal radiation, crucial for understanding nuclear event aftermath.
Area of Science:
- Radiation Biology
- Toxicology
- Genomics
Background:
- Internal radionuclide contamination poses significant health risks following radiation accidents or malicious nuclear events.
- Cesium-137 (137Cs) is a common radionuclide of concern in such scenarios.
Purpose of the Study:
- To investigate the biological effects of internal 137CsCl contamination in mice.
- To characterize dose-rate-dependent and independent gene expression changes in blood over time.
Main Methods:
- Male C57BL/6 mice were injected with varying activities of 137CsCl to achieve different cumulative doses and dose rates over 14 days.
- Whole blood samples were collected at multiple time points (days 2, 3, 5, 7, 14).
- Gene expression profiling was performed using Agilent Mouse Whole Genome microarrays.
Main Results:
- Identified both dose-rate-dependent and independent gene expression patterns in response to 137CsCl.
- Observed a rapid, persistent immune response and B cell depletion, indicative of chronic low-dose-rate irradiation effects.
- Noted activation of pathways related to platelet aggregation and TP53 signaling, though with temporal variability.
Conclusions:
- Gene expression profiling provides insight into the dynamic in vivo response to internal radiation.
- TP53 signaling may play a central role upstream of diverse transcriptional responses.
- Understanding blood cell responses to internal contamination is vital for managing nuclear events.
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