Silencing Cardiac Troponin I-Interacting Kinase Reduces Lipopolysaccharide-Induced Sepsis-Induced Myocardial Dysfunction in Rat by Regulating Apoptosis-Related Proteins.

The aim of this study was to investigate the effect of cardiac troponin I-interacting kinase (TNNI3K) on sepsis-induced myocardial dysfunction (SIMD) and further explore the underlying molecular mechanisms. In this study, a lipopolysaccharide- (LPS-) induced myocardial injury model was used. qRT-PCR was performed to detect the mRNA expression of TNNI3K. Western blot was conducted to quantitatively detect the expression of TNNI3K and apoptosis-related proteins (Bcl-2, Bax, and caspase-3). ELISA was performed to detect the content of lactate dehydrogenase (LDH) and creatine kinase (CK). TUNEL assay was used to detect the apoptosis of H9C2 cells. In LPS-induced H9C2 cells, TNNI3K was up regulated. Besides, the CK activity, the content of LDH, and the apoptosis of H9C2 cells were significantly increased after treatment with LPS. Silencing TNNI3K decreased the LDH release activity and CK activity and inhibited apoptosis of H9C2 cell. Further research illustrated that si-TNNI3K promoted the protein expression of Bcl-2 and decreased the protein expression of Bax and cleaved caspase-3. The study concluded that TNNI3K was upregulated in LPS-induced H9C2 cells. Importantly, functional research findings indicated that silencing TNNI3K alleviated LPS-induced H9C2 cell injury by regulating apoptosis-related proteins.

miR-429 inhibits osteosarcoma progression by targeting HOXA9 through suppressing Wnt/ß-catenin signaling pathway.

Osteosarcoma (OS) is the most commonly diagnosed malignant cancer of bone that occurs in adolescents and children. Mounting number of studies have indicated that miRNAs are increasingly playing fundamental roles in OS development. Thus, the biological function of miR-429 in OS progression was explored. The results of RT-qPCR revealed that miR-429 was downregulated in OS tissues and OS cell lines (MG-63, U2OS, Saos-2) while homeobox A9 (HOXA9) was markedly increased. Moreover, HOXA9 was confirmed as a direct target of miR-429 by using luciferase reporter assay. It was identified that miR-429 exhibited a suppressive effect on OS progression while HOXA9 showed the oncogenic function in OS progression by using MTT and Transwell assays. More importantly, rescue assays manifested that HOXA9 can partially overturn the suppressive effect of miR-429 on OS. Overexpression of miR-429 inhibited the activation of Wnt/ß-catenin signaling pathway. In conclusion, miR-429 suppressed OS progression by targeting HOXA9 through Wnt/ß-catenin pathway.

A facile synthesis of Fe3O4/nitrogen-doped carbon hybrid nanofibers as a robust peroxidase-like catalyst for the sensitive colorimetric detection of ascorbic acid.

In recent years, the fabrication of functional nanostructures with multicomponents for a variety of novel biosensors has received considerable attention due to their synergistic improved sensitivity. Herein, we report a facile approach for the preparation of Fe3O4/nitrogen-doped carbon (Fe3O4/N-C) hybrid nanofibers, and construct a sensing platform for the sensitive colorimetric detection of H2O2 and ascorbic acid (AA). During the synthetic process, a discontinuous layer of polypyrrole (PPy) is first polymerized in situ on the surface of the α-Fe2O3 nanofibers under hydrothermal reaction using α-Fe2O3 nanofibers as both a template and an oxidant. Then the prepared α-Fe2O3/PPy nanofibers are converted into Fe3O4/N-C hybrid nanofibers through pyrolysis with a thermochemical reduction process. The resulting Fe3O4/N-C hybrid nanofibers are used as a novel peroxidase mimic towards the oxidation of 3,3,5,5-tetramethylbenzidine (TMB) in the presence of H2O2, with a superior catalytic activity over individual α-Fe2O3 nanofibers, α-Fe2O3/PPy nanofibers, Fe3O4/C nanofibers, and commercial Fe3O4 nanoparticles. Based on the high peroxidase-like activity of Fe3O4/N-C hybrid nanofibers, a sensing platform for the colorimetric detection of AA is developed. A good linear relationship from 0 to 50 µM and a detection limit of 0.04 µM are achieved. This work offers a new method for the preparation of Fe3O4/N-C hybrid nanofibers and presents new potential applications in biosensing, medical diagnostics and environmental monitoring.

Self-Assembly Fabrication of Coaxial Te@poly(3,4-ethylenedioxythiophene) Nanocables and Their Conversion to Pd@poly(3,4-ethylenedioxythiophene) Nanocables with a High Peroxidase-like Activity.

Here, we report a simple one-step procedure to fabricate coaxial Te@poly(3,4-ethylenedioxythiophene) (PEDOT) nanocables via a self-assembly redox polymerization between 3,4-ethylenedioxythiophene monomer and the oxidant of sodium tellurite without the assistance of any templates and surfactants. The as-synthesized Te@PEDOT coaxial nanocables have diameters of center cores in the range of 5-10 nm, and the size of the outer shell from several nanometers to 15 nm. More interestingly, the as-prepared Te@PEDOT nanocables can be converted to Pd@PEDOT nanocables via a galvanic replacement reaction. The center core of the Pd nanowire exhibits a high crystallinity. The application of the synthesized Pd@PEDOT nanocables as peroxidase-like catalysts for the colorimetric detection of H2O2 is reported. The synergistic effect between the Pd nanowire and electrically conducting PEDOT enhances the catalytic activity toward the oxidation of the peroxidase substrate 3,3',5,5'-tetramethylbenzidine in the presence of H2O2. A detection limit toward H2O2 is as low as 4.83 µM, and a linear range from 10 to 100 µM has been achieved. This work offers a potential versatile route for the fabrication of cable-like nanocomposites with conducting polymers and other active components, which display great promise in applications such as catalysis, nanoelectronic devices, and energy storage and conversion.