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Abstract

To understand the potential impact on risk from exposure to low-level ionizing radiation, we have investigated the modulation of gene expression, induction of DNA damage and of neoplastic transformation in human or rodent cells derived from cultures exposed in vitro to low dose γ-rays (a low linear energy transfer radiation) or very low fluences of α-particles (a high linear energy transfer radiation). Pre-exposure of cells to a low γ-ray dose protected cells from the DNA damaging and killing effects induced by a subsequent acute challenge exposure to γ-rays. Furthermore, a low dose chronic exposure to γ-rays decreased the frequency of micronucleus formation and neoplastic transformation to a level below the spontaneous rate in human and rodent cells respectively. In contrast, when cell cultures were exposed to low fluences of α-particles, wherein a small fraction of cells were irradiated, stressful effects were transmitted from the irradiated to adjoining nonirradiated bystander cells. The mechanisms underlying these effects and their relative contribution to the overall risk to ionizing radiation is discussed.

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