Transient transfection using 222 nm far UV-C irradiation

Ultraviolet (UV) light is never used for gene transfer because it damages DNA and harms cellular and plasmid DNA. A light source selectively radiating Far UV-C (F-UV) light causes less DNA damage. We investigated potential introduction of plasmids into cells by irradiating them with F-UV light. COS-7 and CHO-K1 cells were irradiated with 222 nm F-UV light. Then, DNA solution containing green fluorescent protein (EGFP) plasmid was added to the culture and incubated (37 °C, 5% CO<sub>2</sub>, 24 h) for fluorescence microscopy. Cytotoxicity of cells irradiated with the same energy as for gene transfer was evaluated. Characteristics of EGFP-positive cells were compared with non-transfected cells by propidium iodide (PI) and Hoechst staining. Cells with distinct green fluorescence were observed after F-UV light irradiation and addition of 200 ng of EGFP plasmid. COS-7 cells showed the highest number of EGFP-positive cells at 0.5 mJ/cm<sup>2</sup> irradiation, whereas that for CHO-K1 cells was at 1 mJ/cm<sup>2</sup> irradiation. Cytotoxicity was low in COS-7 at ≤ 1 mJ/cm<sup>2</sup> irradiation and CHO-K1 at ≤ 0.5 mJ/cm<sup>2</sup>. Transfected cells did not incorporate PI, and their nuclei did not differ from those of non-transfected cells. We successfully transfected two cell lines with EGFP plasmids by F-UV irradiation.

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Journal
Scientific Reports
Published
2025-05-14
DOI
https://doi.org/10.1038/s41598-025-00477-6
Primary Topic
Viral Infectious Diseases and Gene Expression in Insects
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article
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article

Transient transfection using 222 nm far UV-C irradiation

Takahiro Yamasaki, Jun Nishikawa, Yu Okada, Toru Koi et al.
Scientific Reports
Viral Infectious Diseases and Gene Expression in Insects
article

Transient transfection using 222 nm far UV-C irradiation

Takahiro Yamasaki, Jun Nishikawa, Yu Okada, Toru Koi, Takeshi Yamamoto, Masaharu Nishimura, Yuki Shimizu, Yoshimasa Ogawa, Tomohiro Fujii, Yutaka Suehiro
article en

Abstract

Ultraviolet (UV) light is never used for gene transfer because it damages DNA and harms cellular and plasmid DNA. A light source selectively radiating Far UV-C (F-UV) light causes less DNA damage. We investigated potential introduction of plasmids into cells by irradiating them with F-UV light. COS-7 and CHO-K1 cells were irradiated with 222 nm F-UV light. Then, DNA solution containing green fluorescent protein (EGFP) plasmid was added to the culture and incubated (37 °C, 5% CO<sub>2</sub>, 24 h) for fluorescence microscopy. Cytotoxicity of cells irradiated with the same energy as for gene transfer was evaluated. Characteristics of EGFP-positive cells were compared with non-transfected cells by propidium iodide (PI) and Hoechst staining. Cells with distinct green fluorescence were observed after F-UV light irradiation and addition of 200 ng of EGFP plasmid. COS-7 cells showed the highest number of EGFP-positive cells at 0.5 mJ/cm<sup>2</sup> irradiation, whereas that for CHO-K1 cells was at 1 mJ/cm<sup>2</sup> irradiation. Cytotoxicity was low in COS-7 at ≤ 1 mJ/cm<sup>2</sup> irradiation and CHO-K1 at ≤ 0.5 mJ/cm<sup>2</sup>. Transfected cells did not incorporate PI, and their nuclei did not differ from those of non-transfected cells. We successfully transfected two cell lines with EGFP plasmids by F-UV irradiation.

Scientific ReportsVol. 15(1)
Yamaguchi University (JP), Ushio (Japan) (JP)
Openalex Percentile: Top 90%
Viral Infectious Diseases and Gene Expression in Insects
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Transient transfection using 222 nm far UV-C irradiation — Takahiro Yamasaki, Jun Nishikawa, et al. · Scientific Reports (2025) | TGRS Research Map | TGRS