253
Views
29
CrossRef citations to date
0
Altmetric
ADAPTATION AND BYSTANDER SIGNALS IN MEDAKA

Exposure to low level chronic radiation leads to adaptation to a subsequent acute X-ray dose and communication of modified acute X-ray induced bystander signals in medaka (Japanese rice fish, Oryzias latipes)

, , &
Pages 1011-1022 | Received 09 Aug 2010, Accepted 09 May 2011, Published online: 23 Sep 2011

References

  • Audette-Stuart M, Yankovich T, Mulpuru S. 2005. Adaptive response in frogs chronically exposed to low doses of ionizing radiation in the environment. Proceedings of the Canadian Nuclear Society 2005. 1–12.
  • Banerjee G, Gupta N, Kapoor A, Raman G. 2005. UV induced bystander signaling leading to apoptosis. Cancer Letters 223:275–284.
  • Biedrzycki ML, Jilany TA, Dudley SA, Bais HP. 2010. Root exudates mediate kin recognition in plants. Communicative and Integrative Biology 3:28–35.
  • Cregan SP, Brown DL, Mitchel REJ. 1999. Apoptosis and the adaptive response in human lymphocytes. International Journal of Radiation Biology 75:1087–1094.
  • Dahle J, Kvam E, Stokke T. 2005. Bystander effects in UV-induced genomic instability: antioxidants inhibit delayed mutagenesis induced by ultraviolet A and B radiation. Journal of Carcinogenesis 9(4):11.
  • Gow MD, Seymour CB, Byun SH, Mothersill CE. 2008. Effect of dose rate on the radiation-induced bystander response. Physics in Medicine and Biology 53:119–132.
  • Harney JV, Seymour CB, Murphy DM, Mothersill C. 1995. Variation in the expression of p53, c-myc, and bcl-2 oncoproteins in individual patient cultures of normal urothelium exposed to cobalt 60 gamma-rays and N-nitrosodiethanolamine. Cancer Epidemiological Biomarkers Preview 4:617–625.
  • Hei TK, Zhou H, Ivanov VN, Hong M, Lieberman HB, Brenner DJ, Amundson SA, Geard CR. 2008. Mechanism of radiation-induced bystander effects: a unifying model. Journal of Pharmacy and Pharmacology 60:943–950.
  • Hinton TG, Coughlin DP, Yi Y, Marsh LC. 2004. Low dose rate irradiation facility: initial study on chronic exposures to medaka. Journal of Envionmental Radioactivity 74:43–55.
  • Iyer R, Lehnert BE. 2002. Alpha-particle-induced increases in the radioresistance of normal human bystander cells. Radiation Research 157:3–7.
  • Joiner MC, Lambin P, Malaise EP, Robson T, Arrand JE, Skov KA, Marples B. 1996. Hypersensitivity to very-low single radiation doses; its relationship to the adaptive response and induced radioresistance. Mutation Research 358:171–183.
  • Joiner MC, Marples B, Lambin P, Short SC, Turesson I. 2001. Low-dose hypersensitivity: current status and possible mechanisms. International Journal of Radiation Oncology 49:379–389.
  • Lyng FM, Seymour CB, Mothersill C. 2002. Initiation of apoptosis in cells exposed to medium from the progeny of irradiated cells: a possible mechanism for bystander-induced genomic instability? Radiation Research 157:365–370.
  • Kadhim MA, Moore SR, Goodwin EH. 2004. Interrelationships amongst radiation-induced genomic instability, bystander effects, and the adaptive response. Mutation Research 568:21–32.
  • Ko M, Lao X-Y, Kapadia R, Elmore E, Redpath JL. 2006. Neoplastic transformation in vitro by low doses of ionizing radiation: role of adaptive response and bystander effects. Mutation Research 597:11–17.
  • Maguire P, Mothersill C, McClean B, Seymour C, Lyng FM. 2007. Modulation of radiation responses by pre-exposure to irradiated cell conditioned medium. Radiation Research 167:485–492.
  • Marples B, Wouters BG, Collis SJ, Chalmers AJ, Joiner MC. 2004. Low-dose hyper-radiosensitivity: a consequence of ineffective cell cycle arrest of radiation-damaged G2-phase cells. Radiation Research 161:247–255.
  • Mitchel RE. 2006. Low doses of radiation are protective in vitro and in vivo: evolutionary origins. Dose Response 4:75–90.
  • Mitchel RE, Burchart P, Wyatt H. 2008. A lower dose threshold for the in vivo protective adaptive response to radiation. Tumorigenesis in chronically exposed normal and Trp53 heterozygous C57BL/6 mice. Radiation Research 170:765–775.
  • Mothersill C, Bucking C, Smith RW, Agnihotri N, O'Neill A, Kilemade M, Seymour CB. 2006. Communication of radiation-induced stress or bystander signals between fish in vivo. Environmental Science and Technology 40:6859–6864.
  • Mothersill C, Moran G, McNeill F, Gow MD, Denbeigh J, Prestwich W, Seymour CB. 2007. A role for bioelectric effects in the induction of bystander signals by ionizing radiation? Dose Response 5:214–229.
  • Mothersill C, Rea D, Wright EG, Lorimore SA, Murphy D, Seymour CB, O'Malley K. 2001. Individual variation in the production of a ‘bystander signal’ following irradiation of primary cultures of normal human urothelium. Carcinogenesis 22:1465–1471.
  • Mothersill C, Seymour C. 1997. Medium from irradiated human epithelial cells but not human fibroblasts reduces the clonogenic survival of unirradiated cells. International Journal of Radiation Biology 71:421–427.
  • Mothersill C, Seymour C. 2010. Eco-systems biology – from the gene to the stream. Mutation Research 687:63–66.
  • Mothersill C, Seymour CB, Joiner MC. 2002. Relationship between radiation-induced low-dose hypersensitivity and the bystander effect. Radiation Research 157:526–532.
  • Mothersill C, Seymour RJ, Seymour CB. 2006. Increased radiosensitivity in cells of two human cell lines treated with bystander medium from irradiated repair-deficient cells. Radiation Research 165:26–34.
  • Mothersill C, Smith RW, Agnihotri N, Seymour CB. 2007. Characterisation of a radiation induced stress response communicated in vivo between zebrafish. Environmental Science and Technology 41: 3382–3387.
  • Mothersill C, Smith RW, Aizawa K, Hinton T, Seymour C. 2009. Communication of radiation-induced signals in vivo between DNA repair deficient and proficient medaka (Oryzias latipes). Environmental Science and Technology 43:3335–3342.
  • Nagasawa H, Little JB. 1999. Unexpected sensitivity to the induction of mutations by very low doses of alpha-particle radiation: evidence for a bystander effect. Radiation Research 152:552–557.
  • Olivieri G, Bodycote J, Wolff S. 1984. Adaptive response of human lymphocytes to low concentrations of radioactive thymidine. Science 223:594–597.
  • Prise KM, O'Sullivan JM. 2009. Radiation-induced bystander signalling in cancer therapy. Nature Reviews Cancer 9:351–360.
  • Raaphorst GP, Boyden S. 1999. Adapative response and its variation in human normal and tumour cells. International Journal of Radiation Biology 75:865–873.
  • Ryan LA, Seymour CB, Mothersill CE. 2009. Investigation of non-linear adaptive responses and split dose recovery induced by ionizing radiation in three human epithelial derived cell lines. Dose Response 7:292–306.
  • Ryan LA, Seymour CB, O'Neill-Mehlenbacher A, Mothersill CE. 2008b. Radiation-induced adaptive response in fish cell lines. Journal of Environmental Radioactivity 99:739–747.
  • Ryan LA, Smith RW, Seymour CB, Mothersill CE. 2008a. Dilution of irradiated cell conditioned medium and the bystander effect. Radiation Research 169:188–196.
  • Salbu B, Denbeigh J, Smith RW, Heier LS, Teien HC, Rosseland BO, Oughton D, Seymour CB, Mothersill C. 2008. Environmentally relevant mixed exposures to radiation and heavy metals induce measurable stress responses in Atlantic salmon. Environmental Science and Technology 42:3441–3446.
  • Sarapultseva EI, Bychkovskaya IB. 2010. Peculiar low-radiation effects as a risk factor: assessment of organism viability in model experiments with Daphnia magna. International Journal of Low Dose Radiation 7:1–9.
  • Schwartz JL. 2007. Variability: the common factor linking low dose-induced genomic instability, adaptation and bystander effects. Mutation Research 616:196–200.
  • Scott BR, Di Palma J. 2006. Sparsely ionizing diagnostic and natural background radiations are likely preventing cancer and other genomic-instability-associated diseases. Dose Response 5:230–255.
  • Skov KA. 1999. Radioresponsiveness at low doses: hypoer-radiuosensitivity and increased radioresistance in mammalian cells. Mutation Research 430:241–253.
  • Smith D, Raaphorst G. 2003. Adaptive responses in human glioma cells assessed by clonogenic survival and DNA strand break. International Journal of Radiation Biology 79:333–339.
  • Smith RW, Wang J, Bucking CP, Mothersill CE, Seymour CB. 2007. Evidence for a protective response in the gill proteome of rainbow trout exposed to X-ray induced bystander signals. Proteomics 7: 4171–4180.
  • Smith RW, Wang J, Mothersill CE, Hinton TG, Aizawa K, Seymour CB. 2011. Proteomic changes in the gills of wild type and transgenic radiosensitive medaka following exposure to direct irradiation and to X-ray induced bystander signals. Biochmica et Biophysica Acta (Proteins and Proteomics) 1814:290–298.
  • Soucek L, Evan GI. 2010. The ups and downs of Myc biology. Current Opinions in Genetics and Development 20:91–95.
  • Streffer C. 2004. Bystander effects, adaptive response and genomic instability induced by prenatal irradiation. Mutation Research 568:79–87.
  • Surinov BP, Isaeva VG, Dukhova NN. 2004. Postirradiation volatile secretions of mice: syngeneic and allogeneic immune and behavioral effects. Bulletin of Experimental Biology and Medicine 138:384–386.
  • Tapio S, Jacob V. 2007. Radioadaptive response revisited. Radiation and Environmental Biophysics 46:1–12.
  • Ueno AM, Vannais DB, Gustafson DL, Wong JC, Waldren CA. 1996. A low, adaptive dose of gamma-rays reduced the number and altered the spectrum of S1− mutants in human-hamster hybrid AL cells. 1996. Mutation Research 358:161–169.
  • Whiteside JR, McMillan TJ. 2009. A bystander effect is induced in human cells treated with UVA radiation but not UVB radiation. Radiation Research 171:204–121.
  • Wolff S. 1998. The adaptive response in radiobiology: evolving insights and implications. Environmental Health Perspectives 106:277–283.
  • Wolff S, Jostes R, Cross FT, Hui TE, Afzal V, Wiencke JK. 1991. Adaptive response of human lymphocytes for the repair of radon-induced chromosomal damage. Mutation Research 250:299–306.
  • Zhou H, Randers-Pehrson G, Waldren CA, Hei TK. 2004. Radiation-induced bystander effect and adaptive response in mammalian cells. Advances in Space Research 34:1368–1372.
  • Zhou H, Xu A, Suzuki M, Randers-Pehrson G, Waldren CA, Hall EJ, Hei TK. 2002. The yin and yan of bystander versus adaptive response: lessons from the microbeam studies. International Congress Series 1236:241–247.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.