52 research outputs found

    EFFECT OF CERULOPLASMIN THE QUANTITATIVE COMPOSITION AND FUNCTIONAL ACTIVITY OF LEUKOCYTES IN ACUTE PHYSICAL LOAD SUBMAXIMAL POWER

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    In experiments on animals have shown that the use of ceruloplasmin in acute submaximal exercise capacity leads to an increase in neutrophilic leukocytes pool with a change in their functional activity. Increased ability to form aggregates of leukocyte, decrease in chemotaxis. Phagocytic function changes ambiguously — activity of phagocytosis increases, and the intensity decreases

    Nova light curves from the Solar Mass Ejection Imager (SMEI) - II. The extended catalogue

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    We present the results from observing nine Galactic novae in eruption with the Solar Mass Ejection Imager (SMEI) between 2004 and 2009. While many of these novae reached peak magnitudes that were either at or approaching the detection limits of SMEI, we were still able to produce light curves that in many cases contained more data at and around the initial rise, peak, and decline than those found in other variable star catalogs. For each nova, we obtained a peak time, maximum magnitude, and for several an estimate of the decline time (t2). Interestingly, although of lower quality than those found in Hounsell et al. (2010a), two of the light curves may indicate the presence of a pre-maximum halt. In addition the high cadence of the SMEI instrument has allowed the detection of low amplitude variations in at least one of the nova light curves

    The ecdysone receptor regulates several key physiological factors in Anopheles funestus

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    BACKGROUND : Malaria is a devastating disease, transmitted by female Anopheles mosquitoes infected with Plasmodium parasites. Current insecticide-based strategies exist to control the spread of malaria by targeting vectors. However, the increase in insecticide resistance in vector populations hinder the efficacy of these methods. It is, therefore, essential to develop novel vector control methods that efficiently target transmission reducing factors such as vector density and competence. A possible vector control candidate gene, the ecdysone receptor, regulates longevity, reproduction, immunity and other physiological processes in several insects, including malaria vectors. Anopheles funestus is a prominent vector in sub-Saharan Africa, however, the function of the ecdysone receptor in this mosquito has not previously been studied. This study aimed to determine if the ecdysone receptor depletion impacts An. funestus longevity, reproduction and susceptibility to Plasmodium falciparum infection. METHODS : RNA interference was used to reduce ecdysone receptor expression levels in An. funestus females and investigate how the above-mentioned phenotypes are influenced. Additionally, the expression levels of the ecdysone receptor, and reproduction genes lipophorin and vitellogenin receptor as well as the immune gene, leucine rich immune molecule 9 were determined in ecdysone receptor-depleted mosquitoes using quantitative polymerase chain reaction. RESULTS : Ecdysone receptor-depleted mosquitoes had a shorter lifespan, impaired oogenesis, were less fertile, and had reduced P. falciparum infection intensity. CONCLUSIONS : Overall, this study provides the first experimental evidence that supports ecdysone receptor as a potential target in the development of vector control measures targeting An. funestus.Additional file 1: Figure S1. Relative EcR expression levels in dsEcR injected An. funestus females compared to dsGFP injected An. funestus females. The EcR gene was knocked down in dsEcR injected An. funestus females as EcR expression levels were drastically reduced compared to the GFP control. Statistically significant knockdown was evident in dsEcR injected An. funestus females 24, 48 and 72 h after injection as EcR expression in dsEcR injected An. funestus females was 0.11 ± 0.006 (p < 0.05), 0.01 ± 0.001 (p < 0.01) and 0.2 ± 0.06 (p < 0.05) respectively when compared to the GFP injected control of 1. This data confirmed EcR knockdown in An. funestus females injected with dsEcR. Data is representative of 2 biological replicates and normalised using an average of RPS7 and RPL19 reference genes. Expression levels calculated using relative quantification method (∆∆Ct). At each time point statistical significance was assessed with the unpaired student’s t-test. *p < 0.05, **p < 0.01. Error bars represent standard deviation.Additional file 2: Figure S2. The highest mating success rate was achieved when An. funestus males and females are combined for 12 days after which no further increases are observed. The percentage mating success rate increased progressively until it reached its highest value of 62.2% after 12 days of mating. After this point, the mating success rate reached a plateau until day 20. Statistical significance was calculated using one-way ANOVA with Tukey’s post hoc analysis to correct for multiple comparison. Data represents the means of 3 biological replicates. Error bars represent standard deviation of means. ns = not statistically significant p > 0.05; ** = p < 0.01; *** = p < 0.001; **** = p < 0.0001. (n) = number of females per time point across 3 biological replicates.Additional file 3: Figure S3. Blood feeding rates did not differ between treatment groups. Insignificant differences amongst treatment groups confirmed that the blood feeding rates did not influence any changes observed in the phenotypes of dsEcR treated An. funestus females (p > 0.05). Statistical significance calculated using an unpaired student’s t-test. Error bars represent standard deviation. ns = not statistically significant p > 0.05.Additional file 4: Table S1. Statistical significance between dsGFP and uninjected controls from the various biological assays conducted.The Department of Science and Innovation (DSI); the National Research Foundation (NRF) South African Research Chairs Initiative; the NRF Communities of Practice and the South African Medical Research Council Strategic Health Innovation Partnerships (SHIP) with funds from DSI.https://malariajournal.biomedcentral.comhj2022BiochemistryGeneticsMicrobiology and Plant PathologyUP Centre for Sustainable Malaria Control (UP CSMC

    Correlations among biodiversity, biomass and other plant community parameters using the phytosociological approach: A case study from the south-eastern Alps

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    The present study deals with the grassland complex of communities which may be found on the limestones in the southeastern Alps; these communities show in fact a particular interest for their high biodiversity degree and for their importance for the traditional land-use economy of the south-European mountain regions. Phytosociological releve´s corresponding to well-defined plant associations have been used in order to get information on the relationships among plant species diversity, biomass, chorotypes, pollination types, functional strategies and soil characteristics. The analysis was carried out both along an altitudinal and a soil evolution gradient. The analysis of the correlations among the variables and the application of the principal component analysis shows a positive correlation between soil parameters and biomass, eurichory, anemogamy and C- and R-strategies; on the contrary, a negative correlation among stenochory, entomogamy and S-strategy with the soil evolution seems to be present. This article shows how the phytosociological approach can be used to get information and knowledge on the correlations between several variables useful to understand the complex nature of the plant communities in order to support management plans

    Knockdown of subunit 3 of the COP9 signalosome inhibits C2C12 myoblast differentiation via NF-KappaB signaling pathway

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    Abstract Background The COP9 signalosome (CSN) is a conserved protein complex composed of 8 subunits designated CSN1-CSN8. CSN3 represents the third subunit of the CSN and maintains the integrity of the complex. CSN3 binds to the striated muscle-specific β1D integrin tail, and its subcellular localization is altered in differentiated skeletal muscle cells. However, the role of CSN3 in skeletal muscle differentiation is unknown. The main goal of this study was to identify whether CSN3 participates in myoblast differentiation and the signalling mechanisms involved using C2C12 cells as a skeletal muscle cell model. Methods Small-hairpin (shRNA) was used to knockdown CSN3 in C2C12 cells. Differentiation was evaluated by immunostaining and confocal microscopy. Markers of differentiation, NF-κB signaling and CSN subunits expression, were assessed by immunoblotting and/or immunostaining. Cell proliferation was analysed by cell counting, flow cytometry and a 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Data were analyzed by one or two-way analysis of variance (ANOVA) followed by post-hoc testing. Results Transduction of C2C12 cells with two distinct CSN3 shRNAs led to the production of two cells lines expressing 7% of CSN3 protein (shCSN3-Low) and 43% of CSN3 protein (CSN3-Med) compared to controls. Knockdown of CSN3 was accompanied by destabilization of several CSN subunits and increased nuclear NF-κB localization. shCSN3-Med cells expressed less myogenin and formed shorter and thinner myotubes. In contrast, the shCSN3-Low cells expressed higher levels of myogenin prior and during the differentiation and remained mononucleated throughout the differentiation period. Both CSN3 knockdown cell lines failed to express sarcomeric myosin heavy chain (MHC) protein during differentiation. The fusion index was significantly higher in control cells than in shCSN3-Med cells, whereas shCSN3-Low cells showed no cell fusion. Interestingly, CSN3 knockdown cells exhibited a significantly slower growth rate relative to the control cells. Cell cycle analysis revealed that CSN3 knockdowns delayed in S phase and had increased levels of nuclear p21/Cip1 and p27/Kip1. Conclusions This study clarifies the first step toward unrevealing the CSN3/CSN-mediated pathways that controls C2C12 differentiation and proliferation. Further in vivo characterization of CSN/CSN3 may lead to the discovery of novel therapeutic target of skeletal muscle diseases such as muscular dystrophies

    The Antitumor Activity of IMGN529, a CD37-Targeting Antibody-Drug Conjugate, Is Potentiated by Rituximab in Non-Hodgkin Lymphoma Models

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    Naratuximab emtansine (IMGN529) is an investigational antibody-drug conjugate consisting of a CD37-targeting antibody conjugated to the maytansine-derived microtuble disruptor, DM1. IMGN529 has shown promising preclinical and clinical activity in non-Hodgkin lymphoma, including diffuse large B-cell lymphoma (DLBCL). Due to the aggressive nature of the disease, DLBCL is often treated with combination therapies to maximize clinical outcomes; therefore, we investigated the potential of combining IMGN529 with both standard-of-care and emerging therapies against multiple oncology-relevant targets and pathways. The strongest enhancement in potency was seen with anti-CD20 antibodies, including rituximab. The combination of IMGN529 and rituximab was more potent than either agent alone, and this combinatorial benefit was associated with increased apoptotic induction and cell death. Additional studies revealed that rituximab treatment increased the internalization and degradation of the CD37-targeting antibody moiety of IMGN529. The combination of IMGN529 and rituximab was highly efficacious in multiple xenograft models, with superior antitumor efficacy seen compared to either agent alone or treatment with R-CHOP therapy. These findings suggest a novel mechanism whereby the potency of IMGN529 can be enhanced by CD20 binding, which results in the increased internalization and degradation of IMGN529 leading to the generation of greater amounts of cytotoxic catabolite. Overall, these data provide a biological rationale for the enhanced activity of IMGN529 in combination with rituximab and support the ongoing clinical evaluation of IMGN529 in combination with rituximab in patients with relapsed and/or refractory DLBCL
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