The microstructures of FeCoNiCrCu high entropy alloy were investigated under directional solidification. The results showed that only diffraction peak corresponding to a FCC crystal structure was observed in the directionally solidified FeCoNiCrCu alloy. With increasing solidification rate, the interface morphology would grows in planar, cellular and dendrite. Comparing the potentiodynamic polarization of as-cast and directionally solidified FeCoNiCrCu high entropy alloy in a 3.5%NaCl solution, it is clearly reveals that the corrosion resistance of directionally solidified FeCoNiCrCu alloy is superior to that of the as-cast FeCoNiCrCu alloy.
Diabetic retinopathy (DR) is one of the severe microvascular complications of diabetes. The protective effects of FA on retinal vascular endothelial cells against high glucose levels involve in multiple aspects in DR; however, the underlying mechanism is not fully elucidated. In present study, we investigated the transcriptome as well as genome-wide DNA methylation and hydroxymethylation signature in human retinal microvascular endothelial ACBRI 181 cells cultured within high glucose (HG) medium supplemented with or without FA by RNA-seq, MeDIP-seq, and hMeDIP-seq. Total 3308 differential expressed genes (DEGs) were involved in multiple biological processes and molecular functions containing angiogenesis, inflammation, S-adenosyl methionine metabolism, and hypoxia response. Moreover, the global DNA methylation and hydroxymethylation in ACBRI 181 cells with FA treatment were both compromised compared to HG. Combined with transcriptome data, four subclusters of DEGs with hyper- or hypomethylated promoters were further verified. Unexpectedly, promoters of these 487 genes all displayed a pattern of increased DNA hydroxymethylation. Furthermore, hyperglycemia rat model was established and administered with FA. The DNA methylation and hydroxymethylation changes of selected target genes COL1A1, ITGA7, MMP-14, and VEGFB confirmed by MeDIP-qPCR were consistent with the results in human ACBRI 181 cells. Finally, the presence of activated DNMT1 and TET2 induced by FA was determined in ACBRI 181 cells and hyperglycemia rat. Taken together, this research provided a resource of expression and epigenetic profiles in retinal microvascular endothelial cell, emphasizing a pharmacological mechanism of FA on DNA methylation and hydroxymethylation regulation in retinal microvessel cells of DR.
The joint surface of the 1060 aluminum and AZ31 magnesium alloy was prepared through friction stir lap welding (FSLW) under different welding process parameters. The joint surface was characterized three-dimensionally using a three-dimensional (3D) optical profiler, and the coordinate data were obtained. The fractal dimension of the joint surface was calculated by the box-width transformation method using a MATLAB program. Furthermore, the influence of the welding process parameters on the fractal dimension of the joint surface was studied. The response surface model was established based on the principle of central composite design (CCD), and analysis of variance (ANOVA) was carried out to test the accuracy of the response surface. The results showed that the joint surface morphology had fractal characteristics, and the fractal dimension could be used as an index to characterize the quality of the joint surface. The change of the welding process parameters had a great impact on the fractal dimension of the joint surface, the interaction between the parameters was small, and the fitting accuracy of the response surface model was high. The fractal dimension of the joint surface decreased with the increase in the welding and rotational speeds and the effect of the rotational speed was more significant.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.