23 research outputs found

    Cellular Radiosensitivity: How much better do we understand it?

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    Purpose: Ionizing radiation exposure gives rise to a variety of lesions in DNA that result in genetic instability and potentially tumorigenesis or cell death. Radiation extends its effects on DNA by direct interaction or by radiolysis of H2O that generates free radicals or aqueous electrons capable of interacting with and causing indirect damage to DNA. While the various lesions arising in DNA after radiation exposure can contribute to the mutagenising effects of this agent, the potentially most damaging lesion is the DNA double strand break (DSB) that contributes to genome instability and/or cell death. Thus in many cases failure to recognise and/or repair this lesion determines the radiosensitivity status of the cell. DNA repair mechanisms including homologous recombination (HR) and non-homologous end-joining (NHEJ) have evolved to protect cells against DNA DSB. Mutations in proteins that constitute these repair pathways are characterised by radiosensitivity and genome instability. Defects in a number of these proteins also give rise to genetic disorders that feature not only genetic instability but also immunodeficiency, cancer predisposition, neurodegeneration and other pathologies. Conclusions: In the past fifty years our understanding of the cellular response to radiation damage has advanced enormously with insight being gained from a wide range of approaches extending from more basic early studies to the sophisticated approaches used today. In this review we discuss our current understanding of the impact of radiation on the cell and the organism gained from the array of past and present studies and attempt to provide an explanation for what it is that determines the response to radiation

    Co-founding ant queens prevent disease by performing prophylactic undertaking behaviour

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    Abstract Background Social insects form densely crowded societies in environments with high pathogen loads, but have evolved collective defences that mitigate the impact of disease. However, colony-founding queens lack this protection and suffer high rates of mortality. The impact of pathogens may be exacerbated in species where queens found colonies together, as healthy individuals may contract pathogens from infectious co-founders. Therefore, we tested whether ant queens avoid founding colonies with pathogen-exposed conspecifics and how they might limit disease transmission from infectious individuals. Results Using Lasius niger queens and a naturally infecting fungal pathogen Metarhizium brunneum, we observed that queens were equally likely to found colonies with another pathogen-exposed or sham-treated queen. However, when one queen died, the surviving individual performed biting, burial and removal of the corpse. These undertaking behaviours were performed prophylactically, i.e. targeted equally towards non-infected and infected corpses, as well as carried out before infected corpses became infectious. Biting and burial reduced the risk of the queens contracting and dying from disease from an infectious corpse of a dead co-foundress. Conclusions We show that co-founding ant queens express undertaking behaviours that, in mature colonies, are performed exclusively by workers. Such infection avoidance behaviours act before the queens can contract the disease and will therefore improve the overall chance of colony founding success in ant queens

    Evaluating the potential of thermal read-out techniques combined with molecularly imprinted polymers for the sensing of low-weight organic molecules

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    In recent years, there has been a tremendous increase in the papers published on synthetic recognition elements. Molecularly imprinted polymers (MIPs), also referred to as “man-made mimics” of antibodies, are able to rebind their template molecules with high affinity. Advantages compared with those of natural receptors include their excellent thermal and chemical stability, low cost, and ease of the production process. However, their use in commercial biosensors is limited owing to the difficulty to incorporate MIPs into suitable sensing platforms and traditional detection techniques, such as chromatography, that require bulky and sophisticated equipment. In this review, we evaluate the potential to use MIPs combined with thermal read-out for the detection of low-weight organic molecules. We discuss thermal methods to study MIP-template complexation and to determine neurotransmitters concentrations. In particular, we highlight the heat-transfer method, a recent technique that is straightforward and low cost and requires minimal instrumentation. Until now, sample preparation involves a 2-step process, making it time-consuming, and measuring biological samples is difficult owing to the noise in the signal. Different sample preparation methods are discussed, and it will be demonstrated how this affects the thermal response. An outlook is given in novel methods that can simplify and speed up sample preparation. Finally, we show a novel thermal technique, which is based on the analysis of transport of thermal waves rather than evaluating the fixed heat-transfer resistance. Through applying the concept of thermal waves, signal-noise ratio is significantly increased, which results in lower detection limits and has potential for the study of biological samples

    Reproductive pattern comparison of Uca thayeri Rathbun, 1900 and U. uruguayensis Nobili, 1901 (Crustacea, Decapoda, Ocypodidae)

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    Ovigerous females of Uca thayeri and U. uruguayensis were used to achieve and compare their reproductive pattern. The females mean size was 6.6 &plusmn; 0.8mm for U. uruguayensis and 17.3&plusmn; 4.4mm for U. thayeri. The mean fecundity obtained for U. uruguayensis was 1883 &plusmn; 490 eggs (N = 27) and for U. thayeri was 31068 &plusmn; 11186 eggs (N = 31). The differences observed in reproductive pattern of U. thayeri and U. uruguayensis suggest an adaptive strategy by each species: U. thayeri presented seasonal reproduction with a pronounced intensity from January to March and higher fecundity, while U. uruguayensis reproduction was continuous all year round, but with lower fecundity.<br>Fêmeas ovígeras de U. thayeri e de U. uruguayensis foram utilizadas para se avaliar e comparar o padrão reprodutivo. O tamanho médio das fêmeas foi de 6,6 &plusmn; 0,8mm para U. uruguayensis, variando de 17,3 &plusmn; 4,4mm para U. thayeri. A fecundidade média obtida para U. uruguayensis foi 1883 &plusmn; 490 ovos (N = 27) e para U. thayeri de 31068 &plusmn; 11185 ovos (N = 31). As diferenças observadas no padrão reprodutivo de U. thayeri e U. uruguayensis sugerem estratégias adaptativas: U. thayeri apresenta uma reprodução sazonal, com atividade pronunciada de janeiro a março e alta fecundidade, enquanto U. uruguayensis reproduz-se continuamente, mas com proles menores
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