Abstract
At present, the comet assay has been applied to Drosophila melanogaster for the in vivo analysis of genotoxicity, using three different larvae cells: hemocyte, midgut, and neuroblast cells. Due to the advantages of this higher eukaryotic organism, in terms of its similarities to mammals in DNA damage response, the comet assay in Drosophila has been successfully used in several studies to analyze the in vivo genotoxicity of chemicals, including chemotherapeutic drugs, environmental contaminants, and metals. The obtained results clearly confirm the usefulness of this combination (Drosophila and comet assay), and open its possibilities for a more widely use, selecting new cell targets and exposure scenarios.
In this context, we present here detailed protocols to perform this assay using neuroblast and hemocyte cells.
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Acknowledgments
The authors thank the financial support of MEC Spain (project CT2004-03005) and FICYT (PCTI Asturias, project PC07-018) to LMS and CIRIT (project 2009SGR-725) to RM. ERC thanks the support of Dirección General de Investigación y Postgrado, UC Temuco, DGIP UCT CD 2010-01 project, and MECESUP UCT 0804 project. LA thanks the support of Instituto Universitario de Oncología del Principado de Asturias, Obra Social Cajastur.
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Sierra, L.M., Carmona, E.R., Aguado, L., Marcos, R. (2014). The Comet Assay in Drosophila: Neuroblast and Hemocyte Cells. In: Sierra, L., Gaivão, I. (eds) Genotoxicity and DNA Repair. Methods in Pharmacology and Toxicology. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-1068-7_15
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DOI: https://doi.org/10.1007/978-1-4939-1068-7_15
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