Association of Base Excision Repair Gene Polymorphisms with ESRD Risk in a Chinese Population

The base excision repair (BER) pathway, containing OGG1, MTH1 and MUTYH, is a major protector from oxidative DNA damage in humans, while 8-oxoguanine (8-OHdG), an index of DNA oxidation, is increased in maintenance hemodialysis (HD) patients. Four polymorphisms of BER genes, OGG1 c.977C > G (rs1052133), MTH1 c.247G > A (rs4866), MUTYH c.972G > C (rs3219489), and AluYb8MUTYH (rs10527342), were examined in 337 HD patients and 404 healthy controls. And the 8-OHdG levels in leukocyte DNA were examined in 116 HD patients. The distribution of MUTYH c.972 GG or AluYb8MUTYH differed between the two groups and was associated with a moderately increased risk for end-stage renal disease (ESRD) (P = 0.013 and 0.034, resp.). The average 8-OHdG/106 dG value was significantly higher in patients with the OGG1 c.977G, MUTYH c.972G or AluYb8MUTYH alleles (P < 0.001 via ANOVA). Further analysis showed that combination of MUTYH c.972GG with OGG1 c.977GG or AluYb8MUTYH increased both the risk for ESRD and leukocyte DNA 8-OHdG levels in HD patients. Our study showed that MUTYH c.972GG, AluYb8MUTYH, and combination of OGG1 c.977GG increased the risk for ESRD development in China and suggested that DNA oxidative damage might be involved in such process

Macrophage polarization states in atherosclerosis

Atherosclerosis, a chronic inflammatory condition primarily affecting large and medium arteries, is the main cause of cardiovascular diseases. Macrophages are key mediators of inflammatory responses. They are involved in all stages of atherosclerosis development and progression, from plaque formation to transition into vulnerable plaques, and are considered important therapeutic targets. Increasing evidence suggests that the modulation of macrophage polarization can effectively control the progression of atherosclerosis. Herein, we explore the role of macrophage polarization in the progression of atherosclerosis and summarize emerging therapies for the regulation of macrophage polarization. Thus, the aim is to inspire new avenues of research in disease mechanisms and clinical prevention and treatment of atherosclerosis

Biosynthesized Ag/alpha-Al2O3 catalyst for ethylene epoxidation: the influence of silver precursors

NSFC [21206140, 21036004]; State Key Laboratory of Advanced Technologies for Comprehensive Utilization of Platinum Metals [SKL-SPM-201210]Biosynthesized Ag/alpha-Al2O3 catalysts toward ethylene epoxidation were prepared with Cinnamomum camphoratrees (CC) extract using AgNO3, silver-ammonia complex ([Ag (NH3)(2)](+)) and silver-ethylenediamine complex ([Ag(en)(2)](+)) as the silver precursors. The catalyst from [Ag(en)(2)](+) demonstrated better activity compared to the catalysts from the other two precursors, 1.41% EO concentration with EO selectivity of 79.1% and 12.0% ethylene conversion were achieved at 250 degrees C. To investigate the influence of silver precursors on the catalytic performance, three catalysts were characterized by XRD, UV-Vis, XPS, SEM and O-2-TPD techniques. The results indicated that [Ag(en)(2)](+) precursors could be reduced more effectively by CC extract, and Ag particles were successfully immobilized onto the alpha-Al2O3 support under mild conditions. Moreover, a silver defects surface on the Ag/alpha-Al2O3 catalyst from [Ag(en)(2)](+) precursors had the best oxygen activation ability, playing an important role in the generation of electrophilic oxygen species which were responsible for the epoxidation reaction of C=C to EO

Biosynthesized Ag/α-Al2O3 catalyst for ethylene epoxidation: The influence of silver precursors

Biosynthesized Ag/α-Al2O3 catalysts toward ethylene epoxidation were prepared with Cinnamomum camphoratrees (CC) extract using AgNO3, silver-ammonia complex ([Ag (NH3) 2]+) and silver-ethylenediamine complex ([Ag(en) 2]+) as the silver precursors. The catalyst from [Ag(en)2]+ demonstrated better activity compared to the catalysts from the other two precursors, 1.41% EO concentration with EO selectivity of 79.1% and 12.0% ethylene conversion were achieved at 250 °C. To investigate the influence of silver precursors on the catalytic performance, three catalysts were characterized by XRD, UV-Vis, XPS, SEM and O 2-TPD techniques. The results indicated that [Ag(en) 2]+ precursors could be reduced more effectively by CC extract, and Ag particles were successfully immobilized onto the α-Al 2O3 support under mild conditions. Moreover, a silver defects surface on the Ag/α-Al2O3 catalyst from [Ag(en)2]+ precursors had the best oxygen activation ability, playing an important role in the generation of electrophilic oxygen species which were responsible for the epoxidation reaction of CC to EO. ? 2014 the Partner Organisations

Microorganism-mediated synthesis of chemically difficult-to-synthesize Au nanohorns with excellent optical properties in the presence of hexadecyltrimethylammonium chloride

Fundamental Research Funds for Central Universities [2010121051]; NSFC [21106117, 21036004]Closely packed, size-controllable and stable Au nanohorns (AuNHs) that are difficult to synthesize through pure chemical reduction are facilely synthesized using a microorganism-mediated method in the presence of hexadecyltrimethylammonium chloride (CTAC). The results showed that the size of the as-synthesized AuNHs could be tuned by adjusting the dosage of the Pichia pastoris cells (PPCs). The initial concentrations of CTAC, ascorbic acid (AA) and tetrachloroaurate trihydrate (HAuCl4 center dot 3H(2)O) significantly affected the formation of the AuNHs. Increasing the diameters of AuNHs led to a red shift of the absorbance bands around 700 nm in their UV-vis-NIR spectra. Interestingly, the AuNH/PPC composites exhibited excellent Raman enhancement such that rhodamine 6G with concentration as low as (10(-9) M) could be effectively detected. The formation process of the AuNHs involved the initial binding of the Au ions onto the PPCs with subsequent reduction by AA to form supported Au nanoparticles (AuNPs) based on preferential nucleation and initial anisotropic growth on the platform of the PPCs. The anisotropic growth of these AuNPs, which was influenced by CTAC and PPCs, resulted in the formation of growing AuNHs, while the secondary nucleation beyond the PPCs produced small AuNPs that were subsequently consumed through Ostwald ripening during the aging of the AuNHs. This work exemplifies the fabrication of novel gold nanostructures and stable bio-Au nanocomposites with excellent optical properties by combining microorganisms and a surfactant

A panel based on three-miRNAs as diagnostic biomarker for prostate cancer

Background: Prostate cancer (PCa) is one of the most prevalent malignancies affecting the male life cycle. The incidence and mortality of prostate cancer are also increasing every year. Detection of MicroRNA expression in serum to diagnose prostate cancer and determine prognosis is a very promising non-invasive modality.Materials and method: A total of 224 study participants were included in our study, including 112 prostate cancer patients and 112 healthy adults. The experiment consisted of three main phases, namely, the screening phase, the testing phase, and the validation phase. The expression levels of serum miRNAs in patients and healthy adults were detected using quantitative reverse transcription-polymerase chain reaction. Receiver operating characteristic (ROC) curves and the area under the curve (AUC) were used to evaluate the diagnostic ability, specificity, and sensitivity of the candidate miRNAs.Result: Eventually, three miRNAs most relevant to prostate cancer diagnosis were selected, namely, miR-106b-5p, miR-129-1-3p and miR-381-3p. We used these three miRNAs to construct a diagnostic panel with very high diagnostic potential for prostate cancer, which had an AUC of 0.912 [95% confidence interval (CI): 0.858 to 0.950; p &lt; 0.001; sensitivity = 91.67%; specificity = 79.76%]. In addition, the three target genes (DTNA, GJB1, and TRPC4) we searched for are also expected to be used for prostate cancer diagnosis and treatment in the future

Fabrication of Au/Pd alloy nanoparticle/Pichia pastoris composites: a microorganism-mediated approach

Fundamental Research Funds for Central Universities [2010121051]; NSFC projects [21106117, 21036004]Synthesis of metal nanoparticles (NPs) is in the limelight in modern nanotechnology. In this present study, bimetallic Au/Pd NP/Pichia pastoris composites were successfully fabricated through a one-pot microbial reduction of aqueous HAuCl4 and PdCl2 in the presence of H-2 as an electron donor. Interestingly, flower-like alloy Au/Pd NP/Pichia pastoris composites were obtained under the following conditions, NaCl concentration 0.9% (w/v), molar ratio of Au/Pd (1 : 2) and the time for pre-adsorption of Au(III) and Pd(II) ions 15 min, through fresh yeast reduction. The mapping results from scanning transmission electron microscopy (STEM) with a high-angle annular dark field detector confirmed that the Au/Pd NPs on the surface of the yeast were indeed alloy. Furthermore, the energy dispersive X-ray (EDX) and X-ray photoelectron spectroscopy (XPS) measurements showed that the composition of the bimetallic NPs were consistent with the initial molar ratio of the precursors

Author Correction: WWP2 regulates pathological cardiac fibrosis by modulating SMAD2 signaling.

An amendment to this paper has been published and can be accessed via a link at the top of the paper

Inhibition of CLIC4 Enhances Autophagy and Triggers Mitochondrial and ER Stress-Induced Apoptosis in Human Glioma U251 Cells under Starvation

CLIC4/mtCLIC, a chloride intracellular channel protein, localizes to mitochondria, endoplasmic reticulum (ER), nucleus and cytoplasm, and participates in the apoptotic response to stress. Apoptosis and autophagy, the main types of the programmed cell death, seem interconnected under certain stress conditions. However, the role of CLIC4 in autophagy regulation has yet to be determined. In this study, we demonstrate upregulation and nuclear translocation of the CLIC4 protein following starvation in U251 cells. CLIC4 siRNA transfection enhanced autophagy with increased LC3-II protein and puncta accumulation in U251 cells under starvation conditions. In that condition, the interaction of the 14-3-3 epsilon isoform with CLIC4 was abolished and resulted in Beclin 1 overactivation, which further activated autophagy. Moreover, inhibiting the expression of CLIC4 triggered both mitochondrial apoptosis involved in Bax/Bcl-2 and cytochrome c release under starvation and endoplasmic reticulum stress-induced apoptosis with CHOP and caspase-4 upregulation. These results demonstrate that CLIC4 nuclear translocation is an integral part of the cellular response to starvation. Inhibiting the expression of CLIC4 enhances autophagy and contributes to mitochondrial and ER stress-induced apoptosis under starvation