Bystander and Delayed Effects after Fractionated Radiation Exposure

Abstract Mothersill, C. and Seymour, C. B. Bystander and Delayed Effects after Fractionated Radiation Exposure. Radiat. Res. 158, 626–633 (2002). Human immortalized keratinocytes were exposed to a range of single or fractionated doses of γ rays from 60Co, to medium harvested from donor cells exposed to these protocols, or to a combination of radiation and irradiated cell conditioned medium (ICCM). The surviving fractions after direct irradiation or exposure to ICCM were determined using a clonogenic assay. The results show that medium harvested from cultures receiving fractionated irradiation gave lower “recovery factors” than direct fractionated irradiation, where normal split-dose recovery occurred. The recovery factor is defined here as the surviving fraction of the cells receiving two doses (direct or ICCM) separated by an interval of 2 h divided by the surviving fraction of cells receiving the same dose in one exposure. After treatment with ICCM, the recovery factors were less than 1 over a range of total doses from 5 mGy–5 Gy. Varying the time between doses from 10 min to 180 min did not alter the effect of ICCM, suggesting that two exposures to ICCM are more toxic than one irrespective of the dose used to generate the response. In certain protocols using mixtures of direct irradiation and ICCM, it was possible to eliminate the bystander effect. If bystander factors are produced in vivo, then they may reduce the sparing effect of the dose fractionation.

[1]  J. Little,et al.  Delayed appearance of lethal and specific gene mutations in irradiated mammalian cells. , 1990, International journal of radiation oncology, biology, physics.

[2]  J. Calkins An unusual form of response in x-irradiated protozoa and a hypothesis as to its origin. , 1967, International journal of radiation biology and related studies in physics, chemistry, and medicine.

[3]  D. Childs,et al.  Changes in sternal marrow following roentgen‐ray therapy to the spleen in chronic granulocytic leukemia , 1954, Cancer.

[4]  D. T. Goodhead,et al.  Transmission of chromosomal instability after plutonium α-particle irradiation , 1992, Nature.

[5]  K. Goh,et al.  Breaks in normal human chromosomes: are they induced by a transferable substance in the plasma of persons exposed to total-body irradiation? , 1968, Radiation research.

[6]  C. Geard,et al.  Targeted cytoplasmic irradiation with alpha particles induces mutations in mammalian cells. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[7]  C. Mothersill,et al.  Medium from irradiated human epithelial cells but not human fibroblasts reduces the clonogenic survival of unirradiated cells. , 1997, International journal of radiation biology.

[8]  Carmel Mothersill,et al.  Relative Contribution of Bystander and Targeted Cell Killing to the Low-Dose Region of the Radiation Dose–Response Curve , 2000, Radiation research.

[9]  C. Mothersill,et al.  Initiation of Apoptosis in Cells Exposed to Medium from the Progeny of Irradiated Cells: A Possible Mechanism for Bystander-Induced Genomic Instability? , 2002, Radiation research.

[10]  E. Wright,et al.  Inflammatory-type responses after exposure to ionizing radiation in vivo: a mechanism for radiation-induced bystander effects? , 2001, Oncogene.

[11]  C. Mothersill,et al.  Individual variation in the production of a 'bystander signal' following irradiation of primary cultures of normal human urothelium. , 2001, Carcinogenesis.

[12]  J. DiPaolo,et al.  Continuous cell lines with altered growth and differentiation properties originate after transfection of human keratinocytes with human papillomavirus type 16 DNA. , 1988, Carcinogenesis.

[13]  J. Hendry,et al.  Genomic instability: potential contributions to tumour and normal tissue response, and second tumours, after radiotherapy. , 2001, Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology.

[14]  C. Mothersill,et al.  Studies of bystander effects in primary uroepithelial cells using a charged-particle microbeam , 2000 .

[15]  K M Prise,et al.  Direct evidence for a bystander effect of ionizing radiation in primary human fibroblasts , 2001, British Journal of Cancer.

[16]  B. Lehnert,et al.  Alpha-Particle-Induced Increases in the Radioresistance of Normal Human Bystander Cells , 2002, Radiation research.

[17]  D. Goodhead,et al.  Inactivation of Haemopoietic Stem Cells by Slow α-particles , 1993 .

[18]  D. Boothman,et al.  When X-ray-inducible proteins meet DNA double strand break repair. , 2001, Seminars in radiation oncology.

[19]  C. Mothersill,et al.  Delayed expression of lethal mutations and genomic instability in the progeny of human epithelial cells that survived in a bystander-killing environment. , 1997, Radiation oncology investigations.

[20]  C. Mothersill,et al.  High yields of lethal mutations in somatic mammalian cells that survive ionizing radiation. , 1986, International journal of radiation biology and related studies in physics, chemistry, and medicine.

[21]  K. Mossman Deconstructing radiation hormesis. , 2001, Health physics.

[22]  M. Barcellos-Hoff,et al.  Extracellular Signaling through the Microenvironment: A Hypothesis Relating Carcinogenesis, Bystander Effects, and Genomic Instability , 2001, Radiation research.

[23]  Carmel Mothersill,et al.  Radiation-Induced Bystander Effects: Past History and Future Directions , 2001, Radiation research.

[24]  B. Lehnert,et al.  Effects of ionizing radiation in targeted and nontargeted cells. , 2000, Archives of biochemistry and biophysics.

[25]  C. Mothersill,et al.  Cell-cell contact during gamma irradiation is not required to induce a bystander effect in normal human keratinocytes: evidence for release during irradiation of a signal controlling survival into the medium. , 1998, Radiation research.

[26]  E. Hall,et al.  Radiobiology for the radiologist , 1973 .

[27]  E. Wright,et al.  Chromosomal instability in unirradiated cells induced in vivo by a bystander effect of ionizing radiation. , 2000, Cancer research.

[28]  J. Little,et al.  High and Low Fluences of α-Particles Induce a G1 Checkpoint in Human Diploid Fibroblasts , 2000 .

[29]  S. Wolff The adaptive response in radiobiology: evolving insights and implications. , 1998, Environmental health perspectives.

[30]  C. Mothersill,et al.  Lethal mutations attributable to misrepair of Q-lesions. , 1988, International journal of radiation biology.