164 research outputs found

    Influence mechanism of epoxy resin and curing agent on high-temperature performance of asphalt

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    To deeply show the internal reasons for the effects of epoxy resin and curing agent on the high-temperature performance of asphalt, nine kinds of asphalt with different content of epoxy resin and curing agent were prepared. On the premise of ensuring that the softening point, penetration and ductility of epoxy asphalt no attenuation, the dynamic shear rheology test and Saybolt viscosity test were used to examine the rutting factor (G*/sin δ), complex shear modulus (G*), phase angle (δ), and viscosity of asphalt with different epoxy resin and curing agent contents. With the help of fluorescence microscopy, microscopic morphology was analyzed, and the micro-image was further analyzed quantitatively by using 3Dsurface and particle statistics. The results show that adding epoxy resin and curing agent into asphalt can significantly improve the rutting factor and complex shear modulus of asphalt and reduce the phase angle and the viscosity growth rate of asphalt changed from fast to slow. Fluorescence and 3Dsurface imaging results indicate when the epoxy resin and the curing agent are uniformly distributed and forms microflocculent structures, the epoxy resin can fully swell in asphalt, and the fluorescence intensity is uniform. The statistical analysis of particles shows that the improvement in high-temperature performance of asphalt by epoxy resin and curing agent results from the distribution of particle area above 26.7346 μm2. The high-temperature performance of epoxy asphalt is optimal when the content of epoxy resin and curing agent is 6 %

    Legume Lectin FRIL Preserves Neural Progenitor Cells in Suspension Culture In Vitro

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    In vitro maintenance of stem cells is crucial for many clinical applications. Stem cell preservation factor FRIL (Flt3 receptor-interacting lectin) is a plant lectin extracted from Dolichos Lablab and has been found preserve hematopoietic stem cells in vitro for a month in our previous studies. To investigate whether FRIL can preserve neural progenitor cells (NPCs), it was supplemented into serum-free suspension culture media. FRIL made NPC grow slowly, induced cell adhesion, and delayed neurospheres formation. However, FRIL did not initiate NPC differentiation according to immunofluorescence and semiquantitive RT-PCR results. In conclusion, FRIL could also preserve neural progenitor cells in vitro by inhibiting both cell proliferation and differentiation

    Reverse genetics construction and pathogenicity of a novel recombinant NADC30-like PRRSV isolated in China

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    China has the largest pig herd in the world which accounts for more than 50% of the global pig population. Over the past three decades, the porcine reproductive and respiratory syndrome virus (PRRSV) has caused significant economic loss to the Chinese swine industry. Currently, the prevalent PRRSV strains in the field are extremely complicated, and the NADC30-like strains, NADC34-like strains, and novel recombinant viruses have become a great concern to PRRS control in China. In this study, a novel NADC30-like PRRSV, named GS2022, was isolated from the lung of a dead pig collected from a farm that experienced a PRRS outbreak. The complete genome of GS2022 shares the highest identity with the NADC30 strain and contains a discontinuous deletion of 131 aa in nsp2. Novel deletion and insertion have been identified in ORF7 and 3’UTR. Recombination analysis revealed that the GS2022 is a potential recombinant of NADC30-like and JXA1-like strains. Both inter-lineage and intra-lineage recombination events were predicted to be involved in the generation of the GS2022. An infectious cDNA clone of GS2022 was assembled to generate the isogenic GS2022 (rGS2022). The growth kinetics of rGS2022 were almost identical to those of GS2022. The pathogenicity of the GS2022 and rGS2022 was evaluated using a nursery piglet model. In the infection groups, the piglets exhibited mild clinical symptoms, including short periods of fever and respiratory diseases. Both gross lesions and histopathological lesions were observed in the lungs and lymph nodes of the infected piglets. Therefore, we reported a novel recombinant NADC30-like PRRSV strain with moderate pathogenicity in piglets. These results provide new information on the genomic characteristics and pathogenicity of the NADC30-like PRRSV in China

    Construction of a prognostic assessment model for colon cancer patients based on immune-related genes and exploration of related immune characteristics

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    Objectives: To establish a novel risk score model that could predict the survival and immune response of patients with colon cancer.Methods: We used The Cancer Genome Atlas (TCGA) database to get mRNA expression profile data, corresponding clinical information and somatic mutation data of patients with colon cancer. Limma R software package and univariate Cox regression were performed to screen out immune-related prognostic genes. GO (Gene ontology) and KEGG (Kyoto Encyclopedia of Genes and Genomes) were used for gene function enrichment analysis. The risk scoring model was established by Lasso regression and multivariate Cox regression. CIBERSORT was conducted to estimate 22 types of tumor-infiltrating immune cells and immune cell functions in tumors. Correlation analysis was used to demonstrate the relationship between the risk score and immune escape potential.Results: 679 immune-related genes were selected from 7846 differentially expressed genes (DEGs). GO and KEGG analysis found that immune-related DEGs were mainly enriched in immune response, complement activation, cytokine-cytokine receptor interaction and so on. Finally, we established a 3 immune-related genes risk scoring model, which was the accurate independent predictor of overall survival (OS) in colon cancer. Correlation analysis indicated that there were significant differences in T cell exclusion potential in low-risk and high-risk groups.Conclusion: The immune-related gene risk scoring model could contribute to predicting the clinical outcome of patients with colon cancer
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