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BackgroundLipid metabolism disorders contribute to the risk factor of prostatic hyperplasia. Lipid ratios have also attracted a lot of attention. Yet, research about the correlation of lipid ratios with prostatic hyperplasia is limited. Hence, the aim of this study was to investigate the association of lipid ratios with the risk of benign prostatic hyperplasia (BPH) in Chinese male subjects.MethodsHealthy men who underwent routine health check-ups from January 2017 to December 2019 were recruited. Twenty-four thousand nine hundred sixty-two individuals were finally enrolled in this research. Binary logistic regression analysis was performed to investigate the relationship between lipid ratios and BPH in Chinese adults.ResultsAfter health examinations for more than 2 years, 18.46% of subjects were ascertained as incident BPH cases. Higher age, body mass index (BMI), prostate-specific antigen (PSA), triglycerides (TGs), low-density lipoprotein cholesterol (LDL-C), triglyceride to high-density lipoprotein cholesterol (TG/HDL-C) ratio, total cholesterol to high-density lipoprotein cholesterol (TC/HDL-C) ratio, and lower high-density lipoprotein cholesterol (HDL-C) were significantly associated with BPH risk, while total cholesterol (TC) was not significant. When quartiles of TG/HDL-C and TC/HDL-C were analyzed in multivariable model, higher TG/HDL-C and TC/HDL-C were associated with a risk of BPH (odds ratio [OR] = 2.11; 95% confidence interval [CI]: 1.89, 2.36; P-trend < 0.001; and OR = 1.67; 95% CI: 1.50, 1.85; P-trend < 0.001, respectively). In addition, stratified analyses based on the general population exhibited that with increasing age (≥35 years) the relationship of TG/HDL-C ratio with BPH risk was dominantly positive (all P-trend < 0.001, P-interaction = 0.001), and significant associations were also found in blood pressure strata and FBG strata (all P-trend < 0.001), except men with BMI ≥ 28 kg/m2 were slightly weakened (OR = 2.01, 95% CI: 1.41, 2.85; P-trend = 0.04). Moreover, there were significant associations between quartiles of TC/HDL-C and the risk of BPH was observed mainly in age 55–64 years, BMI 18.5–23.9 Kg/m2, blood pressure strata, and FBG strata. However, the P-value for a linear trend among those with BMI ≥ 28 Kg/m2 in which participants at the highest quartile of TC/HDL-C had an OR of 1.45 (95% CI: 1.09, 1.93) was 0.594. Additionally, higher TG/HDL-C ratio (≥0.65) may be a risk factor for BPH in China adults of different age decades (≥35 years) with normal TG and HDL-C.ConclusionsTG/HDL-C and TC/HDL-C were associated with BPH risk, TG/HDL-C was a powerful independent risk factor for BPH in Chinese adults, and higher TG/HDL-C ratio should be valued in male subjects with normal TG and HDL-C levels.

The development of low-price and highly efficient catalysts for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) has always been challenging with regard to water splitting. Pyrrhotite Fe7S8 has become a research hotspot due to its abundant reserves, high electrical conductivity and excellent catalytic activity. In general, introducing metal heteroatoms into transition metal sulfides (TMSs) can effectively enhance the activity and stability of TMSs. Herein, Co-doped pyrrhotite Fe7S8 nanosheets were obtained by a straightforward two-step method consisting of hydrothermal treatment followed by subsequent heat treatment. Results from XPS analysis and contact angle measurements showed that doping optimized the chemical environment around iron atoms and enhanced the adsorption of water molecules on the surface of Fe7S8, thereby greatly improving the electrocatalytic efficiency of water electrolysis. Compared with other counterparts, Co0·95Fe6·05S8 exhibited superior OER activity with an overpotential of 311 mV at a current density of 10 mA cm−2, and higher performance towards HER with an overpotential of 284 mV at 10 mA cm−2 in alkaline solution. In sum, Co0·95Fe6·05S8 is promising as a bifunctional catalyst for water splitting under alkaline conditions.

Nanoarchitecture materials are widely investigated to enhance hydrogen evolution reaction (HER) performance. However, it is beset with difficulties to obtain nanomaterials at industrial-scale in comparison with bulk materials. Herein, bulk electrocatalyst Fe4.5Ni4.5S8/Fe7S8 is prepared using flotation method and alkali cleaning from natural nickel ore. Sulfur vacancies and electron interaction between Fe7S8 and Fe4.5Ni4.5S8 may efficiently reduce hydrogen adsorption energy's absolute value, thus significantly improving hydrogen production efficiency. Hybrid catalyst requires ultralow overpotential of 48 mV at 10 mA cm−2 for HER in 0.5 M H2SO4 and exhibits high stability (maintaining an almost constant overpotential after 20,000 cyclic voltammetry sweeps). Therefore, it can be affirmed that it demonstrates promising industrial application as an electrocatalyst towards HER.

Myelin sheath reconstruction plays an important role in peripheral nerve regeneration. But the hindered reconstruction of myelin sheath, due to the inadequate repair phenotypes of macrophages and Schwann cells after peripheral nerve injury, often causes poor functional nerve recovery. Here, biomechanically-adapted immunohydrogels are prepared as the FK506-loaded platforms and nerve tissue engineering scaffolds to reconstruct myelin sheath for peripheral nerve regeneration. By immunofluorescent staining, an increase in the proportion of F4/80

Ethylene-propylene rubber, linear low-density polyethylene and polyolefin elastomer, which are prepared by copolymerization of ethylene with α-olefins, have an important market share of the industry due to their excellent properties. Catalyst plays important role in the copolymerization of ethylene with α-olefins. Many vanadium complexes in the oxidation states of +3, +4 and +5 have been developed as precatalyst for the copolymerization. The progress of vanadium complex catalysts and their use in copolymerization of ethylene with α-olefins were reviewed. The effects of chelated ligands on the catalytic activity of catalysts, composition, molecular weight, molecular weight distribution and sequence of the resulting copolymers were discussed. Vanadium(III) complexes are widely used since vanadium(III) species are usually considered as active species in olefin coordination polymerization. Vanadium(III) complexes bearing monodentate N -heterocyclic carbene (NHC) ligand or bidentate β-diketonate ligands have been used as precatalyst in copolymerization of ethylene with propylene, affording ethylene-propylene copolymers with high propylene content. Ethylene-propylene copolymers with ultra-high molecular weight were prepared by using vanadium(III) complexes containing NHC ligand. Vanadium(III) complexes bearing chelated bidentate N^N or N^O, etc. ligands show high catalytic activity up to 8820 kg mol–1 h–1 toward copolymerization of ethylene with 1-hexene. The introduction of bulky substitutes on the ligand results in an increase in the reactive ratio of ethylene and a decrease in the reactive ratio of 1-hexene, and thus a change in the sequence of monomer in the resulting copolymer. Vanadium(III) complexes containing tridentate and tetradentate ligands display relatively lower catalytic activity than their analogues containing similar bidentate ligand. Most vanadium(IV) complexes display lower catalytic activity than vanadium(III) complexes bearing similar ligands. Ethylene-propylene copolymer with high propylene content could be prepared by copolymerization of ethylene and propylene catalyzed by vanadium(IV) complexes containing monodentate amide ligands. Vanadium(V) complexes bearing chelating aryloxides have been shown to be highly active (up to 144400 kg mol–1 h–1) in copolymerization of ethylene with propylene, affording ethylene-propylene copolymers with low propylene content (less than 15%(mol)). Ethylene-propylene copolymers with high propylene content (more than 30%(mol)) could be prepared by vanadium complexes containing monodentate or bedentate ligands. It is interesting to note that quasi-living copolymerization of ethylene with propylene was realized by using vanadium(V) complexes containing NHC ligand and ethylene-propylene copolymers with ultrahigh molecular weight and narrow molecular weight distribution were obtained. In conclusion, the vanadium complex catalysts have displayed good catalytic behavior towards the copolymerization of ethylene with α-olefins. The vanadium complexes discussed here may be an inspiration for future work in the development of vanadium complex catalyst with high catalytic activity and high comonomer incorporation for copolymerization of ethylene with α-olefins.

Fusobacterium nucleatum (Fn) is a critical colorectal cancer (CRC)-associated bacterium. DNA hunger/stationary phase protective proteins (Dps) are bacterial ferritins that protect DNA from oxidative stress. However, little is known about the regulatory roles of Fn-Dps towards host cellular functions. Here, we identified Fn-Dps from the culture supernatant of Fn by mass spectrometry, and prepared the recombinant of Fn-Dps protein. We show a novel virulence protein of Fn, Fn-Dps, which lyses and disrupts erythrocytes by the competition for iron acquisition. Also, Fn-Dps facilitates intracellular survival of Fn in macrophages by upregulating the expression of the chemokine CCL2/CCL7. In addition, Fn-Dps can elicit a strong humoral immune response, and mucosal immunization with Fn-Dps conferred protection against Fn in the intestinal tract. Moreover, a high level of anti-Fn-Dps antibody was prevalent in populations, and elevated anti-Fn-Dps antibody levels were observed in CRC patients. Furthermore, Fn-Dps promotes the migration of CRC cells via the CCL2/CCL7-induced epithelial-mesenchymal transition (EMT) and promotes CRC metastasis in vivo.

Sustaining efficacious T cell-mediated antitumor immune responses in the tumor tissues is the key to the success of cancer immunotherapy. Current strategies leverage altering the signals T cells sense in the tumor microenvironment (TME). Checkpoint inhibitor-based approaches block inhibitory signals such as PD-1 whereas cytokine-based therapies increase the level of immune-stimulatory cytokines such as IL-2. Besides extrinsic signals, the genetic circuit within T cells also participates in determining the nature and trajectory of antitumor immune responses. Here, we showed that efficacy of the IL33-based tumor immunotherapy was greatly enhanced in mice with T cell-specific Eomes deficiency. Mechanistically, we demonstrated that Eomes deficient mice had diminished proportions of exhausted/dysfunctional CD8+ T cells but increased percentages of tissue resident and stem-like CD8+ T cells in the TME. In addition, the IFNγ+TCF1+ CD8+ T cell subset was markedly increased in the Eomes deficient mice. We further demonstrated that Eomes bound directly to the transcription regulatory regions of exhaustion and tissue residency genes. In contrast to its role in inhibiting T cell immune responses at the tumor site, Eomes promoted generation of central memory T cells in the peripheral lymphoid system and memory recall responses against tumor growth at a distal tissue site. Finally, we showed that Eomes deficiency in T cells also resulted in increased efficacy of PD-1-blockade tumor immunotherapy. In all, our study indicates that Eomes plays a critical role in restricting prolonged T cell-mediated antitumor immune responses in the TME whereas promoting adaptive immunity in peripheral lymphoid organs.

Lamellar and hexagonal–coil–cylinder self-assembled structures of ABA type triblock copolymers containing mesogen-jacketed liquid crystalline polymer (MJLCP) as the rod block, and polyisobutylene (PIB) as the coil middle block were discovered. PIB was synthesized by living cationic polymerization of isobutylene initiated by 1,4-bis(2-chloro-2-propyl)benzene (p-DCC), and then a small amount of styrene was introduced at the end of the PIB chains to form the difunctional PIB macroinitiator with -CH2CH(C6H5)Cl end groups for further atom transfer radical polymerization (ATRP). 2,5-Bis[(4-methoxyphenyl)oxycarbonyl]styrene (MPCS) was block-copolymerized from the difunctional PIB macroinitiators at 110 °C. The molecular characterization of the triblock copolymers was performed with 1H NMR, 13C NMR, gel permeation chromatography (GPC), and thermogravimetric analysis (TGA). Their phase structures and transitions were investigated by differential scanning calorimetry (DSC), small angle X-ray scattering (SAXS), and polarized optical microscopy experiments. It was demonstrated that the triblock copolymers formed lamellar structures at moderate rod fractions and hexagonal coil cylinders in the rod matrix at high rod fractions. The d-spacing of the microphase-separated structures was influenced by the liquid crystalline phase of rod-like PMPCS blocks.

BACKGROUND Gut microbial dysbiosis contributes to the development of colorectal cancer (CRC). We evaluated the utility of fecal bacterial biomarker candidates identified by our 16S rDNA sequencing analysis for CRC diagnosis. METHODS We measured the relative abundance of Fusobacterium nucleatum (Fn), Faecalibacterium prausnitzii (Fp), Bifidobacterium (Bb), and Lactobacillus (Lb) by quantitative PCR in fecal samples from 2 cohorts of 903 individuals. We evaluated and validated the diagnostic performance of these microbial ratios and investigated the antagonistic effect of Fn against 3 different indicator stains. RESULTS The microbial ratio of Fn to Bb (Fn/Bb) had a superior sensitivity of 84.6% and specificity of 92.3% in detecting CRC (area under the curve, AUC = 0.911). The combination of Fn/Bb and Fn/Fp improved the diagnostic value (AUC = 0.943). Moreover, the combination of Fn/Bb and Fn/Fp offered 60.0% specificity and 90.0% sensitivity in detecting stage I of CRC (AUC = 0.804). In particular, Fn was negatively correlated with Fp in the CRC group. The performance for CRC diagnosis was confirmed in the validation cohort II. The culture supernatant from Fn exhibited strong bactericidal activity against probiotics Fp and Bb strains. CONCLUSIONS This study found that Fn could play a role in microbiota dysbiosis via the secreted antagonistic substances against probiotics. Moreover, the ratio of Fn to the important probiotics Fp and Bb was identified as a valuable biomarker for screening early CRC.

We performed dynamic Monte Carlo simulations of random copolymers containing variable sliding mobility of non-crystallizable comonomer sequences (reflecting their relative sizes) in the crystalline monomer regions. Upon raising strains, we observed that the comononer sliding mobility does not affect the strain evolution curves of crystallinity. However, in the middle temperature region, the low mobility causes a delay of switching from the intra-molecular to the inter-molecular modes of crystal nucleation in the copolymers holding low fractions of comonomers. We attributed the effect to the difficulty of comonomers to be excluded from the nucleating domains that are limited by sequence segregation in the oriented amorphous segments. The implication of this effect to the efficiency of crystal nucleation upon cyclic loading has been discussed.

Double perovskite oxides are useful electrode materials in supercapacitors. However, adopting their special structures to improve the electrochemical performances of supercapacitor electrodes is still challenging. In this study, hollow spherical porous La2CoMnO6 (HS-LCMO) materials were prepared using carbon spheres as template impregnation followed by annealing in air to remove the template. The proposed method was advantageous in terms of low-cost, simple operation, large scalability, and improved electrochemical performance of La2CoMnO6. The as-obtained HS-LCMO specimens were tested electrochemically, and the results were compared to reference sample (SG-LCMO) prepared by the sol-gel method. At current density of 1 A g−1, HS-LCMO showed high specific capacitance of 376 F g−1, much higher than that of SG-LCMO (94 F g−1). To expand the application prospects of supercapacitors, HS-LCMO and activated carbon (AC) were then assembled into asymmetric supercapacitors, and their testing exhibited wide potential window of 2 V with high energy density reaching 65.8 Wh kg−1 at 1000 W kg−1. Besides, the supercapacitor devices maintained around 89.2% of the initial capacitance after 3000 cycles. The proposed synthesis strategy looks very promising for preparation of future cathode materials for high-performance supercapacitors.

The advantages of green tires in energy saving, environmental protection and safety make it become the trend of the tire. Neodymium-based high cis -polybutadiene rubber (Nd-BR) and solution styrene-butadiene rubber (SSBR) are two important raw materials for manufacturing green tire. Situation of green tire, progress in the synthesis of Nd-BR and butadiene-based copolymer, current status of some industrialized Nd-BR and development of rare earth catalysts have been reviewed, which is helpful for the production of high-performance synthetic rubber for green tire. The main Nd-BR producers are Lanxess, Versalis, ChiMei, Kumho, Japan Synthetic Rubber, Nizhnekamskneftekhim, Goodyear, Firestone, Sibur, Synthos and Karbochem. The commercial Nd-BR products are normally divided into three grades according to the various Mooney viscosity (ML1+4100°C) of around 45, 55 and 63. Furthermore, the effect of microstructure, composition and topology on processing property, mechanical properties and dynamic mechanical properties of Nd-BR and butadiene-based copolymer were introduced. Stereo-specificity is a key factor for the performance of Nd-BR product. The results of the characteristic relaxation time ( τ ), yield stress ( T y), 300% modulus ( T 300), and T 300/ T y for various Nd-BR indicated that the increase of cis -1,4 content was benefit for the improvement of processing properties. The decrease of Δ G ʹ with an increase in cis -1,4 content indicated that Nd-BR with high cis -1,4 content of around 98.5% behaved low Payne effect, which was mainly attributed to the strong interaction between polymer and filler. Excellent processing performance means that the addition of fillers to rubber compounds are easy to scatter. These can short the mixing time and produce the highest quality product with the lowest possible cost. Nd-BR products with higher cis -1,4 content possess the superior mechanical properties and dynamic mechanical properties of BR vulcanizates, such as modulus at 300%, tensile strength, abrasion resistance, heat build-up, compression properties and rolling resistance and wet-skid resistance. Nd-BR which possesses cis -1,4 content of more than 98% has more excellent mechanical properties, dynamic mechanical properties, and is suitable for green tire as raw materials for the excellent properties such as low heat build-up, rolling power loss, compression deformation, compression ratio and abrasion loss. Long chain branched Nd-BR possesses an improved cold flow resistance, processing performance and mixing performance with the filler. High cis -1,4 butadiene/styrene elastomer and stereospecfic butadiene/styrene copolymer combine excellent performance of Nd-BR and SBR. Both mechanical performance and skid resistance ability on ice road were increased, while rolling resistance was decreased for the vulcanizates. These excellent properties of the synthetic rubbers are beneficial for manufacture of high-performance green tires.

Gut microbial dysbiosis contributes to the development of colorectal cancer (CRC). We evaluated the utility of fecal bacterial biomarker candidates identified by our 16S rDNA sequencing analysis for CRC diagnosis.We measured the relative abundance ofThe microbial ratio ofThis study found that

Tumor-derived exosomes (TEXs) are extracellular vesicles that are continuously released into the blood by tumor cells and carry specific surface markers of the original tumor cells. Substantial evidence has implicated TEXs as attractive diagnostic markers for cancer. However, the detection of TEXs in blood at an early tumor stage is challenging due to their very low concentration. Here, we established a method called PLA-RPA-TMA assay that allows TEXs to be detected with high sensitivity and specificity. Based on two proximity ligation assay (PLA) probes that recognize a biomarker on a TEX, we generated a unique surrogate DNA signal for the specific biomarker, which was synchronously amplified twice by recombinase polymerase amplification (RPA) coupled with transcription-mediated amplification (TMA), and then the products of the RPA-TMA reaction were quantitatively detected using a gold nanoparticle-based colorimetric assay. We established proof-of-concept evidence for this approach using TEXs from nasopharyngeal carcinoma (NPC) cells, with a detection limit of 102 particles/mL, and reported the measurement of plasma Epstein-Barr virus latent membrane protein 1 (LPM1)-positive (LMP1+, accuracy: 0.956) and epidermal growth factor receptor (EGFR)-positive (EGFR+, accuracy: 0.906) TEXs as potent early diagnostic biomarkers for NPC.

We developed a linear combination of two Flory’s melting-point theories, one for stretched and the other for solution polymers, to predict the melting point of stretched solution polymers. The dependences of the melting strains on varying temperatures, polymer volume fractions, and solvent qualities were verified by the onset strains of crystallization in our dynamic Monte Carlo simulations of stretched solution polymers under a constant strain rate. In addition, owing to phase separation before crystallization in a poor solvent, calibration of polymer concentration to the polymer-rich phase appears necessary for the verification. Our results set up a preliminary thermodynamic background for the investigation of the multicomponent effect on strain-induced crystallization of polymers in rubbers and gels as well as on shear-induced crystallization of polymers in solutions and blends.

The self-assembly structures and their transformation of blends of rod−coil−rod triblock copolymers and homopolymers were first detected. Adding coil homopolymers into block copolymers with a lamellar structure resulted in an increase of d-spacing. When coil homopolymers were added into triblock copolymer with a rod continuous hexagonally packed-cylinder structure, lamellar structures were obtained, and the lamellar d-spacing were smaller than that of the original structure. The addition of rod-like homopolymer into the block copolymers with a lamellar structure also resulted in the increase of the d-spacing. As a result of the interdigitation, the rod blocks must rearrange to a larger angle with respect to the interface.

The cationic grafting polymerization of isobutylene (IB) from a poly(vinyl acetate) (PVAc) backbone was initiated by the combination of PVAc with titanium tetrachloride (TiCl4) in methylene chloride (CH2Cl2) solution at –65°C. A mixture of IB homopolymer and PVAc grafted with approximately 9.5% (mol) PIB copolymer was formed. 1H- and 13C-NMR spectra confirmed that IB was successfully grafted from the PVAc backbone. PVAc exhibits both initiation and modification behavior. PVAc acts as a macro-initiator in the polymerization to form the graft copolymer. It also plays a role in the homopolymerization of IB initiated by the combination of residual water with TiCl4 and the product PIB with a narrow molecular weight distribution.

The cationic polymerization of isobutylene coinitiated by Al(i-Bu)Cl2(Al) was carried out in mixed butane–butene fractions at −50 °C. The expected polymerization processes induced by the trace of moisture with Al system in the presence of a small amount of external electron-donor modifiers, such as methyl acrylate (MA) and dimethyl sulfoxide (DMSO), were obtained. The experimental results showed that these polymerizations produced polymers with relatively high number-average molecular weights and narrow molecular weight distributions (1.5–2.2). That the gel permeation chromatography traces of the polymers depended on the types and concentrations of external donors suggested that there existed competitive complexation reactions of various electron donors (H2O, MA, and DMSO) with the Al Lewis acid. The roles of external electron donors were to take part in the initiation step by competitive complexation and to modify the reactivity of the growing chain ends in the propagation step by mediation and/or solvation, which impaired the high reactivity of the original growing chain ends. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 40: 2209–2214, 2002

The cationic polymerizations of isobutylene (IB) initiated by the H2O/TiCl4 in dichloromethane (CH2Cl2) at −30 °C were carried out in the absence and presence of various external electron pair dono...

Industrial semi-crystalline polymers contain various kinds of sequence defects, which behave like non-crystallizable comonomer units on random copolymers. We performed dynamic Monte Carlo simulations of strain-induced crystallization of random copolymers with various contents of comonomers at high temperatures. We observed that the onset strains of crystallization shift up with the increase of comonomer contents and temperatures. The behaviors can be predicted well by a combination of Flory's theories on the melting-point shifting-down of random copolymers and on the melting-point shifting-up of strain-induced crystallization. Our thermodynamic results are fundamentally important for us to understand the rubber strain-hardening, the plastic molding, the film stretching as well as the fiber spinning.