The Release of Bystander Factor(s) from Tissue Explant Cultures of Rainbow Trout (Onchorhynchus mykiss) after Exposure to γ Radiation

Abstract O'Dowd, C., Mothersill, C. E., Cairns, M. T., Austin, B., McClean, B., Lyng, F. M. and Murphy, J. E. J. The Release of Bystander Factor(s) from Tissue Explant Cultures of Rainbow Trout (Onchorhynchus mykiss) after Exposure to γ Radiation. Radiat. Res. 166, 611–617 (2006). The bystander response has been documented in cell lines and cell cultures derived from aquatic species over the past several years. However, little work has been undertaken to identify a similar bystander response in tissue explant cultures from fish. In this study, indirect effects of ionizing γ radiation on tissue explant cultures of fish were investigated. Tissue explants in culture were exposed to 0.5 Gy and 5 Gy γ radiation from a 60Co teletherapy unit. A bystander response in Epithelioma papulosum cyprini (EPC) cells exposed to γ-irradiated tissue conditioned medium from rainbow trout explants was investigated, and the effects on cell survival were quantified by the clonogenic survival assay. Dichlorofluorescein and rhodamine 123 fluorescent dyes were used to identify alterations in reactive oxygen species (ROS) and mitochondrial membrane potential (MMP), respectively. Results indicate a different response for the three tissue types investigated. Clonogenic assay results vary from a decrease in cell survival (gill) to no effect (skin) to a stimulatory effect (spleen). Results from fluorescence assays of ROS and MMP show similarities to clonogenic assay results. This study identifies a useful model for further studies relating to the bystander effect in aquatic organisms in vivo and ex vivo.

[1]  C. Mews New Discoveries and Insights (1999–2007) , 2008 .

[2]  C. Mothersill,et al.  Cytoskeletal Reorganization and Altered Phagocytotic Ability in Primary Cultures of Rainbow Trout Hemopoietic Tissue Exposed to Low-Level Ionizing Radiation , 2005, Radiation research.

[3]  E. Débiton,et al.  Cytotoxic effects of 100 reference compounds on Hep G2 and HeLa cells and of 60 compounds on ECC-1 and CHO cells. I mechanistic assays on ROS, glutathione depletion and calcein uptake. , 2005, Toxicology in vitro : an international journal published in association with BIBRA.

[4]  C. Mothersill,et al.  Genetic Factors Influencing Bystander Signaling in Murine Bladder Epithelium after Low-Dose Irradiation In Vivo , 2005, Radiation research.

[5]  C. Mothersill,et al.  Delayed cell death and bystander effects in the progeny of Chinook Salmon Embryo cells exposed to radiation and a range of aquatic pollutants , 2005, International journal of radiation biology.

[6]  L E Feinendegen,et al.  Evidence for beneficial low level radiation effects and radiation hormesis. , 2005, The British journal of radiology.

[7]  S Sundell-Bergman,et al.  Effects of ionising radiation exposure on plants, fish and mammals: relevant data for environmental radiation protection , 2004, Journal of radiological protection : official journal of the Society for Radiological Protection.

[8]  G. Flik,et al.  Effects of husbandry conditions on the skin colour and stress response of red porgy, Pagrus pagrus , 2004 .

[9]  H. Kawauchi,et al.  Melanin-concentrating hormone signaling systems in fish , 2004, Peptides.

[10]  B. Kaina,et al.  Ionizing radiation-induced E-selectin gene expression and tumor cell adhesion is inhibited by lovastatin and all-trans retinoic acid. , 2004, Carcinogenesis.

[11]  D. Boreham,et al.  Cytogenetic dose-response and adaptive response in cells of ungulate species exposed to ionizing radiation. , 2004, Journal of environmental radioactivity.

[12]  W. Morgan,et al.  Mechanisms of cell death associated with death-inducing factors from genomically unstable cell lines. , 2003, Mutagenesis.

[13]  W. Bonner,et al.  Low-dose radiation: Thresholds, bystander effects, and adaptive responses , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[14]  C. Mothersill,et al.  Early events in the apoptotic cascade initiated in cells treated with medium from the progeny of irradiated cells. , 2002, Radiation protection dosimetry.

[15]  N. Baldini,et al.  In vitro testing of the potential for orthopedic bone cements to cause apoptosis of osteoblast-like cells. , 2002, Biomaterials.

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

[17]  C. Mothersill,et al.  Effect of Low Doses of Ionizing Radiation on Cells Cultured from the Hematopoietic Tissue of the Dublin Bay Prawn, Nephrops norvegicus , 2001, Radiation research.

[18]  C. Mothersill,et al.  Production of a signal by irradiated cells which leads to a response in unirradiated cells characteristic of initiation of apoptosis , 2000, British Journal of Cancer.

[19]  I. Mosse,et al.  Melanin decreases clastogenic effects of ionizing radiation in human and mouse somatic cells and modifies the radioadaptive response , 2000, Radiation and environmental biophysics.

[20]  P. Poindron,et al.  Immune Effects of Low-Dose Radiation: Short-Term Induction of Thymocyte Apoptosis and Long-Term Augmentation of T-Cell-Dependent Immune Responses , 2000, Radiation research.

[21]  L. Cai,et al.  Induction of cell-proliferation hormesis and cell-survival adaptive response in mouse hematopoietic cells by whole-body low-dose radiation. , 2000, Toxicological sciences : an official journal of the Society of Toxicology.

[22]  B. Evers,et al.  The role of NF-κB/IκB proteins in cancer: implications for novel treatment strategies , 1999 .

[23]  J F Knowles,et al.  Long-term irradiation of a marine fish, the plaice Pleuronectes platessa: an assessment of the effects on size and composition of the testes and of possible genotoxic changes in peripheral erythrocytes. , 1999, International journal of radiation biology.

[24]  A. Barnetson,et al.  Comparison between the clonogenic, MTT, and SRB assays for determining radiosensitivity in a panel of human bladder cancer cell lines and a ureteral cell line. , 1999, Radiation oncology investigations.

[25]  Nanxin Li,et al.  Ionizing radiation and short wavelength UV activate NF-kappaB through two distinct mechanisms. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[26]  H. Planel,et al.  Effect of a Continuous Gamma Irradiation at a Very Low Dose on the Life Span of Mice , 1998, Gerontology.

[27]  D. Goodhead,et al.  Chromosomal instability in the descendants of unirradiated surviving cells after alpha-particle irradiation. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[28]  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.

[29]  A. Baldwin,et al.  THE NF-κB AND IκB PROTEINS: New Discoveries and Insights , 1996 .

[30]  J. Borowitz,et al.  Monitoring intracellular nitric oxide formation by dichlorofluorescin in neuronal cells , 1995, Journal of Neuroscience Methods.

[31]  J. Merlin,et al.  Comparison of sulforhodamine B, tetrazolium and clonogenic assays for in vitro radiosensitivity testing in human ovarian cell lines , 1995, Anti-cancer drugs.

[32]  E. Azzam,et al.  Radiation-induced adaptive response for protection against micronucleus formation and neoplastic transformation in C3H 10T1/2 mouse embryo cells. , 1994, Radiation research.

[33]  B. Baguley,et al.  Radiosensitivity of new and established human melanoma cell lines: comparison of [3H]thymidine incorporation and soft agar clonogenic assays. , 1994, European journal of cancer.

[34]  Y. Kurihara,et al.  Cytogenetic adaptive response of cultured fish cells to low doses of X-rays. , 1992, Journal of radiation research.

[35]  H. Ischiropoulos,et al.  Evaluation of the probe 2',7'-dichlorofluorescin as an indicator of reactive oxygen species formation and oxidative stress. , 1992, Chemical research in toxicology.

[36]  R. Macklis,et al.  Radiation hormesis. , 1991, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[37]  J. Lemasters,et al.  Rhodamine 123 as a probe of transmembrane potential in isolated rat-liver mitochondria: spectral and metabolic properties. , 1986, Biochimica et biophysica acta.

[38]  R. Novak,et al.  Spectral and metabolic properties of liver microsomes from imidazole-pretreated rabbits. , 1982, Biochemical and Biophysical Research Communications - BBRC.

[39]  T. Puck,et al.  ACTION OF X-RAYS ON MAMMALIAN CELLS , 1957, The Journal of experimental medicine.