# Gene Expression Changes in the Spleen, Lungs, and Liver of Wistar Rats Exposed to β-Emitted 31SiO2 Particles

**Authors:** Nariaki Fujimoto, Nurislam Mukhanbetzhanov, Sanzhar Zhetkenev, Laura Chulenbayeva, Timur Fazylov, Mikhail Mukhortov, Hitoshi Sato, Kassym Zhumadilov, Valeriy Stepanenko, Andrey Kaprin, Sergey Ivanov, Peter Shegay, Masaharu Hoshi, Almagul Kushugulova

PMC · DOI: 10.3390/ijms26062693 · International Journal of Molecular Sciences · 2025-03-17

## TL;DR

This study examines how β-emitted 31SiO2 particles affect gene expression in the spleen, lungs, and liver of rats, focusing on biological impacts similar to those from atomic bomb residual radiation.

## Contribution

The study introduces new insights into the biological effects of β-emitted 31SiO2 particles as a model for residual radiation.

## Key findings

- 31SiO2 exposure significantly increased Cth gene expression in the liver on days 3 and 14.
- The effects of β-emitted particles were most pronounced in the liver compared to other organs.
- Internal exposure to β-emitted microparticles shows potential roles in residual radiation effects.

## Abstract

To understand the biological effects of residual radioactivity after the atomic bomb explosion in Hiroshima and Nagasaki, we previously investigated the effects of 56Mn, a major residual radioisotope. Our rat study demonstrated that inhalation exposure to 56MnO2 microparticles affected gene expression in the lungs, testes, and liver, despite the low radiation doses. Because 56Mn is a β- and γ-emitter, the differential effects between β- and γ-rays should be clarified. In this study, 31Si, a β-emitter with a radioactive half-life similar to that of 56Mn, was used to determine its effects. Male Wistar rats were exposed to sprayed neutron-activated 31SiO2 microparticles, stable SiO2 microparticles, or X-rays. The animals were examined on days 3 and 14 after irradiation. The expression of radiation-inducible marker genes, including Ccng1, Cdkn1a, and Phlda3, was measured in the spleen, lungs, and liver. Furthermore, the expressions of pathophysiological marker genes, including Aqp1, Aqp5, and Smad7 in the lungs and Cth, Ccl2, and Nfkb1 in the liver, were determined. Impacts of 31SiO2 exposure were observed mainly in the liver, where the expression of Cth markedly increased on post-exposure days 3 and 14. Our data suggest that internal exposure to β-emitted microparticles has significant biological effects and its possible roles as residual radiation after atomic bombing.

## Linked entities

- **Genes:** CCNG1 (cyclin G1) [NCBI Gene 900], CDKN1A (cyclin dependent kinase inhibitor 1A) [NCBI Gene 1026], PHLDA3 (pleckstrin homology like domain family A member 3) [NCBI Gene 23612], AQP1 (aquaporin 1 (Colton blood group)) [NCBI Gene 358], AQP5 (aquaporin 5) [NCBI Gene 362], SMAD7 (SMAD family member 7) [NCBI Gene 4092], CTH (cystathionine gamma-lyase) [NCBI Gene 1491], CCL2 (C-C motif chemokine ligand 2) [NCBI Gene 6347], NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790]
- **Chemicals:** SiO2 (PubChem CID 24261)

## Full-text entities

- **Genes:** Ccl2 (C-C motif chemokine ligand 2) [NCBI Gene 24770] {aka MCP-1, MCP1, Scya2, Sigje}, Aqp1 (aquaporin 1) [NCBI Gene 25240] {aka CHIP28}, Smad7 (SMAD family member 7) [NCBI Gene 81516] {aka Madh7}, Ccng1 (cyclin G1) [NCBI Gene 25405] {aka CYCG, Ccng}, Nfkb1 (nuclear factor kappa B subunit 1) [NCBI Gene 81736] {aka EBP-1, NF-kB, NFKB-p50, p50}, Aqp5 (aquaporin 5) [NCBI Gene 25241], Phlda3 (pleckstrin homology-like domain, family A, member 3) [NCBI Gene 363989], Cdkn1a (cyclin-dependent kinase inhibitor 1A) [NCBI Gene 114851] {aka Cip1, UV96, Waf1}
- **Chemicals:** 31Si (MESH:C000615305), SiO2 (MESH:D012822), 31SiO2 (-)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11942150/full.md

## References

36 references — full list in the complete paper: https://tomesphere.com/paper/PMC11942150/full.md

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Source: https://tomesphere.com/paper/PMC11942150