Phenotypic and transcriptional changes in lens epithelial cells following acute and fractionated ionizing radiation exposure.

Autor:	Vigneux G; Biomolecular Sciences Program, Laurentian University, Sudbury, Ontario, Canada., Laframboise T; School of Natural Sciences, Laurentian University, Sudbury, Ontario, Canada., Tharmalingam S; Biomolecular Sciences Program, Laurentian University, Sudbury, Ontario, Canada.; School of Natural Sciences, Laurentian University, Sudbury, Ontario, Canada.; Northern Ontario School of Medicine (NOSM) University, Sudbury, Ontario, Canada.; Health Sciences North Research Institute, Sudbury, Ontario, Canada., Thome C; Biomolecular Sciences Program, Laurentian University, Sudbury, Ontario, Canada.; School of Natural Sciences, Laurentian University, Sudbury, Ontario, Canada.; Northern Ontario School of Medicine (NOSM) University, Sudbury, Ontario, Canada.; Health Sciences North Research Institute, Sudbury, Ontario, Canada.
Jazyk:	angličtina
Zdroj:	International journal of radiation biology [Int J Radiat Biol] 2024; Vol. 100 (4), pp. 573-583. Date of Electronic Publication: 2024 Jan 30.
DOI:	10.1080/09553002.2023.2295965
Abstrakt:	Purpose: Exposure to ionizing radiation is one of the known risk factors for the development of lens opacities. It is believed that radiation interactions with lens epithelial cells (LEC) are the underlying cause of cataract development, however, the exact mechanisms have yet to be identified. The aim of this study was to investigate how different radiation dose and fractionation impact normal LEC function. Materials and Methods: A human derived LEC cell line (HLE-B3) was exposed to a single acute x-ray dose (0.25 Gy) and 6 fractionated doses (total dose of 0.05, 0.1, 0.25, 0.5, 1, and 2 Gy divided over 5 equal fractions). LEC were examined for proliferation using a 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay and migration using a Boyden chamber assay at various time points (0.25, 0.5, 1, 2, 4, 7, 9, 11, and 14 d) post-irradiation. Transcriptomic analysis through RNA sequencing was also performed to identify differentially expressed genes and regulatory networks in cells following 4 different acute exposures and 1 fractionated exposure. Results: Exposure to an acute dose of 0.25 Gy significantly increased proliferation and migration rates, peaking at 7 d post irradiation (20% and 240% greater than controls, respectively), before returning to baseline levels by day 14. Fractionated exposures had minimal effects up to a dose of 0.5 Gy, but significantly reduced proliferation and migration after 1 and 2 Gy by up to 50%. The largest transcriptional response occurred 12 h after an acute 0.25 Gy dose, with 362 genes up-regulated and 288 genes down-regulated. A unique panel of differentially expressed genes was observed between moderate versus high dose exposures, suggesting a dose-dependent transcriptional response in LEC that is more pronounced at lower doses. Gene ontology and upstream regulator analysis identified multiple biological processes and molecular functions implicated in the radiation response, in particular differentiation, motility, receptor/ligand binding, cell signaling and epithelial-mesenchymal cell transition. Conclusions: Overall, this research provides novel insights into the dose and fractionation effects on functional changes and transcriptional regulatory networks in LEC, furthering our understanding of the mechanisms behind radiation induced cataracts.
Databáze:	MEDLINE
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