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Low-Dose Ionizing Radiation Modulates Translation Efficiency in Human Lung Fibroblasts
Radiation Research
|April 3, 2026
Summary
Low-dose ionizing radiation (≤ 0.1 Gy) alters cellular responses by selectively changing messenger RNA (mRNA) translation efficiency, not global protein synthesis. This reveals translation as a sensitive indicator of early radiation effects.
Area of Science:
- Cellular Biology
- Radiation Biology
- Molecular Biology
Background:
- Understanding cellular responses to low-dose ionizing radiation (≤ 0.1 Gy) is critical for radiation protection.
- High-dose radiation impacts gene expression and protein synthesis, but low-dose effects are less understood.
Purpose of the Study:
- To investigate the cellular impact of low-dose ionizing radiation exposure.
- To determine if low-dose radiation affects protein synthesis and gene expression.
- To identify specific molecular targets responding to low-dose radiation.
Main Methods:
- Ribosome profiling was employed on human lung fibroblast cells.
- Cells were exposed to low (0.1 Gy) and high (1 Gy) doses of 60Cobalt gamma (γ) rays.
- Analysis was conducted at 1 and 6 hours postirradiation.
Main Results:
- Global protein synthesis remained unchanged at low doses (0.1 Gy) at 1 and 6 hours postirradiation.
- Specific messenger RNAs (mRNAs) exhibited altered translation efficiency, indicating changes at the translational level.
- Transcriptional changes were minimal, highlighting translation as a more sensitive readout of early low-dose γ-radiation effects.
- The small GTP-binding protein RAB33B was identified as a translationally upregulated target.
Conclusions:
- Low-dose ionizing radiation primarily affects cellular responses through selective mRNA translation, not global protein synthesis.
- Conventional transcriptome analyses may not fully capture the dynamic gene expression changes induced by low-dose radiation.
- Selective translation plays a significant role in the distinct cellular response to low-dose irradiation.

