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Cell inactivation by heavy charged particles

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Summary

The inactivation of cells resulting in lethal or aberrant effects by charged particles is of growing interest. Charged particles at extremely high LET are capable of completely eliminating cell-type and cell-line differences in repair capacity. It is still not clear however whether the repair systems are inactivated, or merely that heavy-ion lesions are less repairable. Studies correlating the particle inactivation dose of radioresistant cells with intact DNA analyzed with pulse field gel electrophoresis and other techniques may be useful, but more experiments are also needed to assess the fidelity of repair. For particle irradiations between 40–100 keV/µm there is however evidence for particle-induced activation of specific genes in mammalian cells, and certain repair processes in bacteria. New data are available on the inactivation of developmental processes in several systems including seeds, and cells of the nematodeC. elegans. Future experimental and theoretical modeling research emphasis should focus on exploring particle-induced inactivation of endpoints assessing functionality and not just lethality, and on analyzing molecular damage and genetic effects arising in damaged but non-inactivated survivors. The discrete nature of selective types of particle damage as a function of radiation quality indicates the value of accelerated ions as probes of normal and aberrant biological processes. Information obtained from molecular analyses of damage and repair must however be integrated into the context of cellular and tissue functions of the organism.

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  1. Cell and Molecular Biology Division, Lawrence Berkeley Laboratory, Building 70A-1118, 94720, Berkeley, CA, USA

    Eleanor A. Blakely

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Invited paper given on the fourth workshop on “Heavy Charged Particles in Biology and Medicine” GSI, Darmstadt, FRG, September 23–25, 1991

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Blakely, E.A. Cell inactivation by heavy charged particles. Radiat Environ Biophys 31, 181–196 (1992). https://doi.org/10.1007/BF01214826

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