224 research outputs found

    Subtitling Gender Stereotypes into English: The Case of Comedy Italian Style

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    Building on the research framework of the Descriptive Translation Studies, this thesis discusses the ways in which gender stereotypes in the cinematic genre of Comedy Italian Style have been subtitled into English. Developing from the late 1950s to the early 1970s and reaching its climax in the 1960s, the Commedia all’italiana is a cinematographic genre which centres on the satire of a rapidly changing society by targeting booming consumerism, entrenched religious and civil institutions, old gender stereotypes and new sexual mores. Comedy Italian Style therefore constitutes an ideal audiovisual corpus to explore the potential manipulation of gender that can result from the subtitling activity and this study focuses on the seven films released by the Criterion Collection. The analysis pays special attention to the strategies used by professionals when dealing with gender representation, and avails itself of a taxonomy of translation strategies for culture-specific references, modified and adapted for the translation of gender stereotypes. Ultimately, the main goal of the study is to gauge the degree of similarity or discrepancy that can be found between the way gender stereotypes are conveyed in the original and in the subtitled versions, and to assess whether the subtitled versions transmit the same, or different, gender stereotypes. The main questions addressed in the analysis are whether the gender stereotypes are kept, modified or deleted and whether the gender representation in the subtitled versions is similar, reinforced or softened. One of the principal trends highlighted in this thesis is the tendency to maintain source culture and intercultural gender stereotypes through the use of literal translation, although the extent to which other gender stereotypes are deleted, manipulated or even added to the subtitled versions of the films is also noteworthy considering the traditional perception of subtitling as a translation mode which remains closer to the source text

    IRE1α deficiency promotes tumor cell death and eIF2α degradation through PERK dipendent autophagy

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    Sensors of endoplasmic reticulum (ER) stress function in a co-ordinated manner. In the present study we investigated the relationship between IRE1α and PERK pathways and survival of ER stressed U937 cells and BC3 cells. To this end, we investigated the effects of a subcytotoxic concentration of Tunicamycin in IRE1α-proficient and in IRE1α-deficient cells, by pharmacological inhibition with 4μ8 C or down-regulation by specific siRNA. We show that either type of IRE1α deficiency affects eIF2α expression and causes cell death increase. GSK2606414, a PERK inhibitor, and PERK specific siRNA prevent eIF2α down-regulation and restore cell survival. Degradation of this protein is due to autophagy, as it is prevented by bafilomycin and not by proteasome inhibition. Furthermore, activation of the autophagy flux is PERK dependent. Also the Cathepsin B inhibitor CA074 prevents eIF2α from degradation and reduces cell death. Altogether, these results show that IRE1α deficiency in ER stressed cells leads to an unexpected decrease of eIF2α, an important molecule for protein translation, through PERK dependent autophagy. Thus, IRE1/XBP1 inhibitors may represent a feasible strategy for tumor therapy, while PERK inhibitors may vanish the goal

    FUS mutant human motoneurons display altered transcriptome and microRNA pathways with implications for ALS pathogenesis

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    The FUS gene has been linked to amyotrophic lateral sclerosis (ALS). FUS is a ubiquitous RNA-binding protein, and the mechanisms leading to selective motoneuron loss downstream of ALS-linked mutations are largely unknown. We report the transcriptome analysis of human purified motoneurons, obtained from FUS wild-type or mutant isogenic induced pluripotent stem cells (iPSCs). Gene ontology analysis of differentially expressed genes identified significant enrichment of pathways previously associated to sporadic ALS and other neurological diseases. Several microRNAs (miRNAs) were also deregulated in FUS mutant motoneurons, including miR-375, involved in motoneuron survival. We report that relevant targets of miR-375, including the neural RNA-binding protein ELAVL4 and apoptotic factors, are aberrantly increased in FUS mutant motoneurons. Characterization of transcriptome changes in the cell type primarily affected by the disease contributes to the definition of the pathogenic mechanisms of FUS-linked ALS

    Forcing scale invariance in multipolarization SAR change detection

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    This paper considers the problem of coherent (in the sense that both amplitudes and relative phases of the polarimetric returns are used to construct the decision statistic) multi-polarization SAR change detec- tion starting from the availability of image pairs exhibiting possible power mismatches/miscalibrations. The principle of invariance is used to characterize the class of scale-invariant decision rules which are insensitive to power mismatches and ensure the Constant False Alarm Rate (CFAR) property. A maximal invariant statistic is derived together with the induced maximal invariant in the parameter space which significantly compress the data/parameters domain. A Generalized Likelihood Ratio Test (GLRT) is synthesized both for the cases of two- and three-polarimetric channels. Interestingly, for the two-channel case, it is based on the comparison of the condition number of a data-dependent matrix with a suitable threshold. Some additional invariant decision rules are also proposed. The performance of the considered scale-invariant structures is compared to those from two non- invariant counterparts using both simulated and real radar data. The results highlight the robustness of the proposed method and the performance tradeoff involve

    Inactivation of Dekkera bruxellensis yeasts in wine storage in brand new oak barrels using low electric current technology

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    Dekkera bruxellensis is one of the species of yeast, which is most damaging to wine quality, and the tools available to control its growth are limited. In previous studies, non-Saccharomyces yeasts and Dekkera bruxellensis have been significantly restricted during wine-making processes using an innovative approach based on low electric current treatment (LEC). In the present study, LEC techniques were assessed for their capacity to inhibit wine spoilage by D. bruxellensis and to prevent formation of undesirable flavours during storage in oak barrels. Although the effect of SO2 treatment on D. bruxellensis viability and ATP content was more immediate, from the 30th day onward no significant variations between LEC and SO2 treatments were observed. At the end of the trial, LEC treatment had had a comparable effect to that of SO2 addition. Acetic acid content was significantly lower after LEC and SO2 treatments than in untreated wines and volatile phenols were also found to be significantly lower in the LEC treated wine. Moreover, the results from the panel test clearly indicate that no significant differences were found between the LEC and the SO2 treated wines. These results clearly indicate that LEC technology could represent a viable tool to limit yeast spoilage caused by D. bruxellensis. The present work represents, to our knowledge, the first attempt to control D. bruxellensis during red wine storage in oak barrels using LEC. The potential industrial applications of LEC technology include the real future possibility of producing a new, marketable range of healthier wines to satisfy the requirements of modern wine consumers

    MicroRNAs-Proteomic Networks Characterizing Human Medulloblastoma-SLCs

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    Medulloblastoma (MB) is the most common malignant brain tumor of pediatric age and is characterized by cells expressing stem, astroglial, and neuronal markers. Among them, stem-like cells (hMB-SLCs) represent a fraction of the tumor cell population with the potential of self-renewal and proliferation and have been associated with tumor poor prognosis. In this context, microRNAs have been described as playing a pivotal role in stem cells differentiation. In our paper, we analyze microRNAs profile and genes expression of hMB-SLCs before and after Retinoic Acid- (RA-) induced differentiation. We aimed to identify pivotal players of specific pathways sustaining stemness and/or tumor development and progression and integrate the results of our recent proteomic study. Our results uncovered 22 differentially expressed microRNAs that were used as input together with deregulated genes and proteins in the Genomatix Pathway System (GePS) analysis revealing 3 subnetworks that could be interestingly involved in the maintenance of hMB-SLCs proliferation. Taken together, our findings highlight microRNAs, genes, and proteins that are significantly modulated in hMB-SLCs with respect to their RA-differentiated counterparts and could open new perspectives for prognostic and therapeutic intervention on MB

    The long noncoding RNA linc-NeD125 controls the expression of medulloblastoma driver genes by microRNA sponge activity

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    Long noncoding RNAs (lncRNAs) are major regulators of physiological and disease-related gene expression, particularly in the central nervous system. Dysregulated lncRNA expression has been documented in several human cancers, and their tissue-specificity makes them attractive candidates as diagnostic/prognostic biomarkers and/or therapeutic agents. Here we show that linc-NeD125, which we previously characterized as a neuronal-induced lncRNA, is significantly overexpressed in Group 4 medulloblastomas (G4 MBs), the largest and least well characterized molecular MB subgroup. Mechanistically, linc-NeD125 is able to recruit the miRNA-induced silencing complex (miRISC) and to directly bind the microRNAs miR-19a-3p, miR-19b-3p and miR-106a-5p. Functionally, linc-NeD125 acts as a competing endogenous RNA (ceRNA) that, sequestering the three miRNAs, leads to de-repression of their targets CDK6, MYCN, SNCAIP, and KDM6A, which are major driver genes of G4 MB. Accordingly, linc-NeD125 downregulation reduces G4 cell proliferation. Moreover, we also provide evidence that linc-NeD125 ectopic expression in the aggressive Group 3 MB cells attenuates their proliferation, migration and invasion. This study unveils the first lncRNA-based ceRNA network in central nervous system tumours and provides a novel molecular circuit underlying the enigmatic Group 4 medulloblastoma

    Consequences of simulated microgravity in neural stem cells: biological effects and metabolic response.

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    Objective: Microgravity was often shown to cause cell damage and impair cell cycle in a variety of biological systems. Since the effects on the neural system were poorly investigated, we aimed to gain insight into how biological processes such as cell cycle, cell damage, stemness features and metabolic status are involved in neural stem cells (NSC) when they experience simulated microgravity. We also wished to investigate whether these modulations were transient or permanent once cells were returned to normal gravity. Methods: NSC were isolated from mouse cerebella and cultured in the Rotary Cell Culture System (RCCS) to model microgravity. We analyzed cell cycle, stress and apoptotic response. We also performed a 1H NMR-based metabolomic analysis and evaluation of stemness features of NSC in simulated microgravity and once in the returned to normogravity cell culture. Results: Biological processes and metabolic status were modulated by simulated microgravity. Cells were arrested in S-phase together with enhanced apoptosis. Metabolic changes occurred in NSC after simulated microgravity. Interestingly, these modulations were transient. Indeed, stemness features and metabolic footprint returned to basal levels after few days of culture in normal conditions. Moreover NSC clonogenic ability was not impaired. Conclusions: Our data suggest that simulated microgravity impacts on NSC biological processes, including cell cycle and apoptosis. However, NSC does not suffer from permanent damage

    Determination of Mycotoxins in Plant-Based Meat Alternatives (PBMAs) and Ingredients after Microwave Cooking

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    In this study, we investigate the role of microwave cooking in reducing mycotoxin contamination in plant-based food matrices, with a focus on veggie burgers (purchased and home-made) and their ingredients (soybean, potatoes, zucchini, carrots). Two different conditions were studied (Max–Min) that were 800 W for 60 s and 800 W for 90 s, respectively. The degradation patterns of aflatoxins (AFB1, AFB2, AFG1, AFG2), fumonisins (FB1, FB2, FB3), trichothecenes (T2, HT2, ZEA), and ochratoxin A (OTA) were studied. The extraction procedures were conducted with the QuEChERS extraction, and the analyses were conducted with liquid chromatography–tandem mass spectrometry (LC-MS/MS). Principal component analysis (PCA) showed that degradation under microwave cooking varies considerably across different food matrices and cooking conditions. This study provides valuable insights into the degradation of mycotoxins during microwave cooking and underscores the need for more research in this area to ensure food safety
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