Three dimensional spider-web-like superconducting filamentary paths in KxFe2−ySe2K_xFe_{2-y}Se_2 single crystals

Since the discovery of high temperature superconductivity in F-doped LaFeAsO, many new iron based superconductors with different structures have been fabricated2. The observation of superconductivity at about 32 K in KxFe2-ySe2 with the iso-structure of the FeAs-based 122 superconductors was a surprise and immediately stimulated the interests because the band structure calculation8 predicted the absence of the hole pocket which was supposed to be necessary for the theoretical picture of S+- pairing. Soon later, it was found that the material may separate into the insulating antiferromagnetic K2Fe4Se5 phase and the superconducting phase. It remains unresolved that how these two phases coexist and what is the parent phase for superconductivity. In this study we use different quenching processes to produce the target samples with distinct microstructures, and apply multiple measuring techniques to reveal a close relationship between the microstructures and the global appearance of superconductivity. In addition, we clearly illustrate three dimensional spider-web-like superconducting filamentary paths, and for the first time propose that the superconducting phase may originate from a state with one vacancy in every eight Fe-sites with the root8*root10 parallelogram structure.Comment: 22 pages, 7 figure

miR-126 promotes angiogenesis and attenuates inflammation after contusion spinal cord injury in rats

AbstractMicroRNAs are a class of small RNAs that regulate the expression of target mRNAs by inhibiting translation or destabilizing target mRNAs. miR-126 is a microRNA that is highly enriched in endothelial cells. miR-126 has been found to promote angiogenesis and inhibit vascular inflammation in endothelial cells by repressing three target genes Sprouty-related EVH1 domain-containing protein 1 (SPRED1), phosphoinositol-3 kinase regulatory subunit 2 (PIK3R2), and vascular cell adhesion molecule 1 (VCAM1). Our previous study showed that the expression of miR-126 was downregulated after spinal cord injury (SCI). Therefore, we wanted to examine whether upregulation of miR-126 could promote angiogenesis, inhibit inflammation, and exert a positive effect on recovery after contusion SCI. In this study, we found that increased levels of miR-126 promoted angiogenesis, and inhibited leukocyte extravasation into the injured spinal cord, which was concurrent with downregulation of mRNA and protein expression of three validated miR-126 target genes, SPRED1, PIK3R2, and VCAM1. Moreover, a dose-dependent effect of miR-126 was observed in rescuing tissue damage and improving the functional deficit after SCI. Thus, the present study indicated that miR-126 played an important role in angiogenesis and inflammation after SCI