17 research outputs found

    TEAD1-dependent expression of the FoxO3a gene in mouse skeletal muscle

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    <p>Abstract</p> <p>Background</p> <p><it>TEAD1 </it>(TEA domain family member 1) is constitutively expressed in cardiac and skeletal muscles. It acts as a key molecule of muscle development, and trans-activates multiple target genes involved in cell proliferation and differentiation pathways. However, its target genes in skeletal muscles, regulatory mechanisms and networks are unknown.</p> <p>Results</p> <p>In this paper, we have identified 136 target genes regulated directly by TEAD1 in skeletal muscle using integrated analyses of ChIP-on-chip. Most of the targets take part in the cell process, physiology process, biological regulation metabolism and development process. The targets also play an important role in MAPK, mTOR, T cell receptor, JAK-STAT, calcineurin and insulin signaling pathways. TEAD1 regulates <it>foxo3a </it>transcription through binding to the M-CAT element in <it>foxo3a </it>promoter, demonstrated with independent ChIP-PCR, EMSA and luciferase reporter system assay. In addition, results of over-expression and inhibition experiments suggest that <it>foxo3a </it>is positively regulated by TEAD1.</p> <p>Conclusions</p> <p>Our present data suggests that TEAD1 plays an important role in the regulation of gene expression and different signaling pathways may co-operate with each other mediated by TEAD1. We have preliminarily concluded that TEAD1 may regulate <it>FoxO3a </it>expression through calcineurin/MEF2/NFAT and IGF-1/PI3K/AKT signaling pathways in skeletal muscles. These findings provide important clues for further analysis of the role of <it>FoxO3a </it>gene in the formation and transformation of skeletal muscle fiber types.</p

    Fecal Metabolomics and Potential Biomarkers for Systemic Lupus Erythematosus

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    The role of metabolomics in autoimmune diseases has been a rapidly expanding area in researches over the last decade, while its pathophysiologic impact on systemic lupus erythematosus (SLE) remains poorly elucidated. In this study, we analyzed the metabolic profiling of fecal samples from SLE patients and healthy controls based on ultra-high-performance liquid chromatography equipped with mass spectrometry for exploring the potential biomarkers of SLE. The results showed that 23 differential metabolites and 5 perturbed pathways were identified between the two groups, including aminoacyl-tRNA biosynthesis, thiamine metabolism, nitrogen metabolism, tryptophan metabolism, and cyanoamino acid metabolism. In addition, logistic regression and ROC analysis were used to establish a diagnostic model for distinguishing SLE patients from healthy controls. The combined model of fecal PG 27:2 and proline achieved an area under the ROC curve of 0.846, and had a good diagnostic efficacy. In the present study, we analyzed the correlations between fecal metabolic perturbations and SLE pathogenesis. In summary, we firstly illustrate the comprehensive metabolic profiles of feces in SLE patients, suggesting that the fecal metabolites could be used as the potential non-invasive biomarkers for SLE

    Effect of laser parameters on fatigue crack growth behavior of AZ31B magnesium alloy TIG welded bionic joint

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    The purpose of this study was to evaluate the effect of laser parameters on the fatigue crack growth (FCG) behavior of AZ31B Magnesium alloy TIG welded bionic joints with ‘soft-hard’ alternating structures prepared by laser bionic treatment (LBT). The changes of laser parameters promoted the growth of fine equiaxed grain with random texture, and average grain size was 5.12 ± 0.51–8.19 ± 1.02 μm, which significantly increased isotropy and microhardness. The average microhardness was 66.5 ± 1.68–70.85 ± 1.41 HV0.1, which increased by more than 23.11% compared with untreated welded joints. For bionic welded joints, the heat-affected zone (HAZ) had higher FCG resistance and cycle times than weld metal (WM), and the specimens with notch in the HAZ showed obvious crack deflection. It was found that FCG behavior showed significant microstructure sensitivity by comparing the FCG rate curve and crack opening displacement. The Paris parameters had a significant linear relationship and effectively reflect the FCG resistance of the different specimens. The fatigue fracture showed that the crack growth zone was mainly dominated by typical cleavage steps and secondary cracks. The fatigue fracture region contains quasi-cleavage and ductile fracture. A series of strengthening mechanisms were induced by LBT and could significantly affect FCG behavior, which promoted crack deflection and branching to increase the toughness of the joint, while the laser remelting zone increased the strength of the joint. Therefore, the synergistic effect of strength-toughness of the joint was obtained by LBT, which provided a new idea for optimizing the bionic design and improving the fatigue property of welded joints

    Highly Active PdNi/RGO/Polyoxometalate Nanocomposite Electrocatalyst for Alcohol Oxidation

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    A PdNi/RGO/polyoxometalate nanocomposite has been successfully synthesized by a simple wet-chemical method. Characterizations such as transmission electron microscopy, energy dispersive X-ray spectroscopy, X-ray diffraction analysis, and X-ray photoelectron spectroscopy are employed to verify the morphology, structure, and elemental composition of the as-prepared nanocomposite. Inspired by the fast-developing fuel cells, the electrochemical catalytic performance of the nanocomposite toward methanol and ethanol oxidation in alkaline media is further tested. Notably, the nanocomposite exhibits excellent catalytic activity and long-term stability toward alcohol electrooxidation compared with the PdNi/RGO and commercial Pd/C catalyst. Furthermore, the electrochemical results reveal that the prepared nanocomposite is attractive as a promising electrocatalyst for direct alcohol fuel cells, in which the phosphotungstic acid plays a crucial role in enhancing the electrocatalytic activities of the catalyst
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