The long-term “fate” of normal human cells after single hits of charged particles is one of the oldest unsolved issues in radiation protection and cellular radiobiology. Using a high-precision heavy-ion microbeam we could target normal human fibroblasts with exactly one or five carbon ions and measured the early cytogenetic damage and the late behaviour using single-cell cloning. Around 70% of the first cycle cells presented visible aberrations in mFISH after a single ion traversal and about 5% of the cells were still able to form colonies. In one third of selected high-proliferative colonies we observed clonal (radiation-induced) aberrations. Terminal differentiation and markers of senescence (PCNA, p16) in the descendants of cells traversed by one carbon ion occurred earlier than in controls, but no evidence of radiation-induced chromosomal instability was found. We conclude that cells surviving single-ion traversal, often carrying clonal chromosome aberrations, undergo accelerated senescence but maintain chromosomal stability.
The Fate of a Normal Human Cell Traversed by a Single Charged Particle
C. Fournier,S. Zahnreich,D. Kraft,T. Friedrich,K. Voss,M. Durante,S. Ritter
Published 2012 in Scientific Reports
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- Publication year
2012
- Venue
Scientific Reports
- Publication date
2012-09-10
- Fields of study
Biology, Medicine, Physics, Environmental Science
- Identifiers
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- Source metadata
Semantic Scholar, PubMed
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