188 research outputs found

    Criminals, Classrooms, and Kangaroo Courts: Why College Campuses Should Not Adjudicate Sexual Assault Cases

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    Elucidating the role of a novel DNA-binding protein identified in the diatom Thalassiosira pseudonana for coping with nutrient and temperature stress

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    Diatoms are associated with nutrient rich waters with high biomass that are commonly found at high latitudes, in coastal waters, in upwelling zones or during seasonal blooms.They display an opportunistic growth described as a ’bloom and bust’ life cyce and a remarkable diversity. These caracteristics are considered to be responsible for their success in aquatic environments and the reason why they contribute about 20% of global primary production and allow them to quickly dominate phytoplankton communities when environmental conditions become favourable. The processes that enable this impressive plasticity of diatoms in response to environmental variability are mostly unknown. A novel conserved DNA binding protein (BIG1) was recently identified and found to differentially regulate genes involved in progression through the cell cycle in centric diatoms as well as about 30% of genes found in natural centric diatom blooms. In our study we show that the BIG1 protein is linked to the regulation of initiation of fast growth upon nutrient addition. Overexpression of BIG1 in the model centric diatom Thalassiosira pseudonana enabled fast recovery and growth after a period of nitrogen stravation and exposure to low and high temperature as well as fostered growth under suboptimal temperatures. We present evidence that BIG1 has an impact on photosynthesis and suggest its involvement in directing the photosynthetic electron flow around Photosystem I. Our results may provide insights into regulatory processes that govern diatoms’ oportunistic growth

    In vivo testing of novel vaccine prototypes against Actinobacillus pleuropneumoniae

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    Actinobacillus pleuropneumoniae (A. pleuropneumoniae) is a Gram-negative bacterium that represents the main cause of porcine pleuropneumonia in pigs, causing significant economic losses to the livestock industry worldwide. A. pleuropneumoniae, as the majority of Gram-negative bacteria, excrete vesicles from its outer membrane (OM), accordingly defined as outer membrane vesicles (OMVs). Thanks to their antigenic similarity to the OM, OMVs have emerged as a promising tool in vaccinology. In this study we describe the in vivo testing of several vaccine prototypes for the prevention of infection by all known A. pleuropneumoniae serotypes. Previously identified vaccine candidates, the recombinant proteins ApfA and VacJ, administered individually or in various combinations with the OMVs, were employed as vaccination strategies. Our data show that the addition of the OMVs in the vaccine formulations significantly increased the specific IgG titer against both ApfA and VacJ in the immunized animals, confirming the previously postulated potential of the OMVs as adjuvant. Unfortunately, the antibody response raised did not translate into an effective protection against A. pleuropneumoniae infection, as none of the immunized groups following challenge showed a significantly lower degree of lesions than the controls. Interestingly, quite the opposite was true, as the animals with the highest IgG titers were also the ones bearing the most extensive lesions in their lungs. These results shed new light on A. pleuropneumoniae pathogenicity, suggesting that antibody-mediated cytotoxicity from the host immune response may play a central role in the development of the lesions typically associated with A. pleuropneumoniae infections

    Современные взгляды на ультразвуковую диагностику внутреннего эндометриоза

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    Представлен обзор данных о применении различных методик в диагностике эндометриоза. Показаны преимущества и высокая информативность трансвагинальной эхографии. Описаны эхографические критерии различных стадий эндометриоза. Отмечена связь эндометриоза с разными патологиями щитовидной и молочной желез.This paper reviews the data on the use of different techniques of endometriosis diagnosis. The advantages and high informativity of transvaginal ultrasonography are demonstrated. Ultrasonography criteria of different stages of endometriosis are described. Association of endometriosis and thyroid and breast pathology is demonstrated

    Identification of autoantibodies to the I protein of the heterogeneous nuclear ribonucleoprotein complex in patients with systemic sclerosis

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    Objective. To assess the presence of autoantibodies to the I protein (polypyrimidine-tract binding protein) of the heterogeneous nuclear RNPs (hnRNP) in different connective tissue diseases. Antibodies to other hnRNP proteins (A1, A2, and B) have been previously found in patients with rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), and mixed connective tissue disease (MCTD). Methods. Sera from 101 patients with various connective tissue diseases and 25 normal controls were investigated by enzyme-linked immunosorbent assay and immunoblotting, for their reactivity to highly purified recombinant hnRNP I. Moreover, reactivity to cellular hnRNP I protein was investigated by immunoblotting using a partially purified preparation of hnRNP proteins (including A1, A2, B, and I), and by indirect immunofluorescence. For the analysis of the fluorescence pattern, affinity-purified antibodies to hnRNP I, obtained from a selected patient, were tested on HEp-2 cells. Results. By immunoblotting, antibodies reacting to recombinant hnRNP I were found in 22 of 40 patients with systemic sclerosis (SSc), 3 of 32 with RA, 0 of 23 with SLE, and 0 of 6 with MCTD. Antibodies to recombinant hnRNP I were more frequently found in patients with pre-SSc or limited SSc (15 of 24) than in those with intermediate or diffuse SSc (7 of 16). In indirect immunofluorescence studies, affinity-purified anti-hnRNP I autoantibodies gave a diffuse nucleoplasmic staining. Using an hnRNP preparation from nuclear extracts, anti-hnRNP I reactivity was detectable in SSc sera, while it was not detectable in RA, SLE, and MCTD sera reacting with hnRNP A/B proteins. Conclusion. Human autoimmune sera show distinct patterns of anti-hnRNP reactivity, i.e., anti-A/B in SLE and RA sera, and anti-I in SSc sera. This suggests that A/B proteins and the I protein may be involved in different dynamic hnRNP complexes that elicit different autoimmune responses. From a clinical perspective, anti-hnRNP I antibodies are frequently associated with pre-SSc features, suggesting an early appearance of these antibodies during the course of the disease
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