Bystander-Type Effects Mediated by Long-Lived Inflammatory Signaling in Irradiated Bone Marrow

Shubhra Rastogi, Philip J. Coates, Sally A. Lorimore, Eric G. Wright

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    Abstract

    Rastogi, R., Coates, P. J., Lorimore, S. A. and Wright, E. G. Bystander-Type Effects Mediated by Long-Lived Inflammatory Signaling in Irradiated Bone Marrow. Radiat. Res. 177, 244-250 (2012).

    Radiation-induced bystander and abscopal effects, in which DNA damage is produced in nonirradiated cells as a consequence of communication with irradiated cells, indicate mechanisms of inducing damage and cell death additional to the conventional model of deposition of energy in the cell nucleus at the time of irradiation. In this study we show that signals generated in vivo in the bone marrow of mice irradiated with 4 Gy gamma rays 18 h to 15 months previously are able to induce DNA damage and apoptosis in nonirradiated bone marrow cells but that comparable signals are not detected at earlier times postirradiation or at doses below 100 mGy. Bone marrow cells of both CBA/Ca and C57BL/6 genotypes exhibit responses to signals produced by either irradiated CBA/Ca or C57BL/6 mice, and the responses are mediated by the cytokines FasL and TNF-alpha converging on a COX-2-dependent pathway. The findings are consistent with indirect inflammatory signaling induced as a response to the initial radiation damage rather than to direct signaling between irradiated and nonirradiated cells. The findings also demonstrate the importance of studying tissue responses when considering the mechanisms underlying the consequences of radiation exposures. (C) 2012 by Radiation Research Society

    Original languageEnglish
    Pages (from-to)244-250
    Number of pages7
    JournalRadiation Research
    Volume177
    Issue number3
    DOIs
    Publication statusPublished - Mar 2012

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