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The flow process of recycling a degraded LiFePO4 cathode.

Enabling the sustainable recycling of LiFePO4 from spent lithium-ion batteries via a one-step oxidation leaching process endowed with better environmental and economic returns.

Histone H3 monoaminylations at glutamine(Q) 5 represent an important family of epigenetic markers in neurons that play critical roles in the mediation of permissive gene expression (1, 2). We previously demonstrated that H3Q5 serotonylation(ser) and dopaminylation(dop) are catalyzed by the Transglutaminase 2 (TGM2) enzyme and alter both local and global chromatin states (3, 4). Here, we found that TGM2 additionally functions as an “eraser” of H3 monoaminylations that is capable of “re-writing” these epigenetic marks in cells, including a new class of this modification, H3Q5 histaminylation(his), which displays dynamic diurnal expression in brain and contributes to neural rhythmicity. We found that H3Q5his inhibits binding of the MLL1 complex to the H3 N-terminus and attenuates its methyltransferase activity on H3 lysine(K) 4. We determined that H3Q5 monoaminylation dynamics are dictated by local monoamine concentrations, which are utilized by TGM2. Taken together, we present here a novel mechanism through which a single chromatin regulatory enzyme is capable of sensing chemical microenvironments to affect the epigenetic states of cells.One sentence summaryA single enzyme, TGM2, bidirectionally controls H3 monoaminylation dynamics, which, in turn, facilitate neural rhythmicity.

Aerobic glycolysis, also known as the Warburg effect, is a hallmark of cancer and essential for metabolism in malignancies, but its regulation and modulation in cancer cells remain poorly understood. Here, using large-scale functional screening, we identified a tumor-associated and broadly expressed oncogenic long noncoding RNA LINC00973. Notably, knocking down LINC00973 significantly inhibits the proliferation of multiple types of cancer cells and reduces tumor growth in vivo. Mechanistically, LINC00973 directly binds to lactate dehydrogenase A (LDHA), an essential glycolytic enzyme, and enhances its enzymatic activity, thereby promoting glycolysis. Clinically, high expression of LINC00973 is significantly associated with poor prognosis in many types of human cancers. This work demonstrates that LINC00973 modulates cancer-specific regulation of the Warburg effect, and may represent a potential target for broad-acting anti-cancer therapies.

The large-scale and efficient synthesis of MnPO4·H2O is an urgent problem to be solved. In this paper, self-assembled dumbbell-shaped MnPO4·H2O particles were successfully synthesized just using KMnO4 and commercial concentrated H3PO4, and then employed as the precursor to prepare LiMnPO4/C composites. The XRD, SEM, TEM, and electrochemical performance tests were used to investigate MnPO4·H2O and the corresponding LiMnPO4/C. The formation mechanism of MnPO4·H2O was discussed. The results showed that temperature and water content have a significant effect on the yield, purity, and morphology of MnPO4·H2O. The synthesized LiMnPO4/C with reduced carbon content at 650 °C delivered a discharge capacity of 109.3 mA h g-1 at 1 C and 104.3 mA h g-1 at 2 C. This green and efficient synthesis method of MnPO4·H2O provides a new idea for the large-scale preparation of LiMnPO4/C cathode materials.

There is a pressing need around the world to develop novel functional biodegradable materials to separate oil/water mixtures and emulsions completely. Recently, superhydrophilicity and underwater superoleophobicity materials have been attracted attention due to their high efficiency in oil/water separation. However, it is still a challenge to prepare materials that combine oil/water separation and water purification in an environment-friendly way. In this work, biodegradable starch-based nanospheres (SNPs) coated filter paper was prepared in a low-cost, simple, and environmentally friendly manner. The SNPs coating could not only help to change the wettability of the substrate material but also build the hierarchical micro and nano structures which are conducive to separation and purification process. After modification by coating SNPs, the filter paper exhibited excellent performance in a wide range of oil/water mixtures or emulsions separation and the wettability of the filter paper could be regulated by adjusting the pH value. The modified filter paper presented good recyclability after several separation process. Furthermore, the as-prepared filter paper could also remove water-soluble contaminants during the oil/water separation process, thus realizing to combine separation and purification process in one single step. This biodegradable starch-based separating material with good separation performance, stability and recyclability has significant application potential in practical separation and purification process.

Ni-rich LiNi0.8 Co0.15 Al0.05 O2 (NCA) material attracts extensive attention due to its high discharge specific capacity, but its distinct drawbacks of rapid capacity decline and poor cycle performance at elevated temperatures and high voltage during charge/discharge cycling restricts its widespread application. To solve these problems, a multifunctional coating layer composed of a lithium-ion-conductive lithium polyacrylate (LiPAA) inner layer and a cross-linked polymer outer layer from certain organic substances of silane-coupling agent (KH550) and polyacrylic acid (PAA) is successfully designed on the surface of NCA materials, which is favorable for eliminating residual lithium and improving lithium-ion conductivity, surface stability, and hydrophobicity of NCA materials. In addition, the amount of the coating material is also investigated. A series of characterization methods such as XRD, FTIR, SEM, TEM, and X-ray photoelectron spectroscopy are used to analyze the morphologies and structures for materials of pristine and modified NCA. It is revealed that the co-coating layer plays a vital part in reducing the surface residual alkalis and improving the stability of NCA particles; as a result, the modified NCA exhibits a greatly improved rate capability, cycle performance, and low polarization impedance.

Cloud-radiative forcing (CRF) at the top of the atmosphere (TOA) over the western Pacific warm pool (WP) shows unique characteristics in response to El Nino events. In this region, the responses of CRF to El Nino events have been a useful metric for evaluating climate models. Satellite data are used to analyze the CRF anomalies to El Nino events simulated by the new and old versions of the Climate System Model of the Chinese Academy of Meteorological Sciences (CAMS-CSM), which has participated in the Atmospheric Model Intercomparison Project (AMIP). Here, simulations for super El Nino years, El Nino years, and normal years are compared with observations. The results show that the mean values of both longwave CRF (LWCRF) and shortwave CRF (SWCRF) in CAMS-CSM are weaker than the observations for each category of El Nino events. Compared with the old version of CAMS-CSM, the decrease in LWCRF during El Nino events is well simulated by the new version of CAMS-CSM. However, both new and old models cannot reproduce the anomalous SWCRF in El Nino events. The biases in the CRF response to El Nino events are attributed to the biases in the cloud vertical structure because of a weaker crash of the Walker circulation in CAMS-CSM. Due to the modification of the conversion rate from cloud droplets to raindrops in the cumulus convection scheme, the new version of CAMS-CSM has better CRF skills in normal years, but biases in El Nino events still exist in the new version. Improving the response of the Walker circulation to El Nino events is key to higher skills in simulating the cloud radiative responses.

Pickering high internal phase emulsions (HIPEs) stabilized solely by bioderived starch-based particles hold potential for application in the food and pharmaceutical fields. This paper reports the use of a thermoresponsive 2-hydroxy-3-butoxypropyl starch (HBPS) particle as a representative natural biocompatible material for use as an effective stabilizer for HIPE formation. HBPS is synthesized by using butyl glycidyl ether as a hydrophobic reagent to change the hydrophobic–hydrophilic balance of starch, and then starch-based particles are fabricated by a simple nanoprecipitation procedure. The size of particles increased with an increase in temperature, and the particles are essentially monodisperse with a PDI of about 0.1 when the temperature was above 15 °C. These HBPS particles were subsequently used as an effective stabilizer to fabricate stable oil-in-water (o/w) Pickering HIPEs with an internal phase volume of 80% at different stabilizer concentrations. The results demonstrated that increasing the particle concentration is conducive to the formation of stable Pickering HIPEs with greater stiffnesses. In addition, the nutraceutical material (β-carotene) was encapsulated into HIPEs and in vitro release experiments revealed that the release in this system can be controlled by adjusting the temperature.

Using different products of disc thickness and Yb ions concentration, we report on the laser performance of Yb:YAG crystals under room and cryogenic temperatures. The optimum crystal parameters have been realized. With a thickness of 0.8 mm, 15 at. % Yb ions doping concentration laser crystal, high optical to optical efficiency of 85.2% and slope efficiency of 89.0% have been achieved and the maximum output energy was 75.6 mJ at ∼ 80 K. Furthermore, the wavelength-switching phenomenon was observed owing to a lower loss cavity with the temperature reduction. Calculation results from the model based on the rate equations were well consistent with the laser output performance. The wavelength-switching effect was also explained by this model.

To realize intelligent and low-cost protective materials, the development of compounds with smart stress-responsive properties and self-healing abilities over a wide temperature range is a major research goal. In this study, a series of impact hardening polymers (IHPs) with stress-responsive properties and self-healing ability in low temperature were synthesized via the condensation copolymerization of silicone polymers with various chain lengths and boron contents. The results of rheological analysis indicate that the IHPs have self-healing ability at low temperatures (healing times of less than 30 h and healing efficiencies better than 80% at −25 °C). Moreover, the relative shear stiffening effect (RSTe), which describes the stress-responsive ability of the IHP, exceeded 2000. In addition, the self-healing mechanism of IHP was investigated by Fourier transform infrared spectroscopy microscopy and pulsed 1H-NMR measurements. The results suggested that reversible dynamic cross-linking arising from the boron compound and the reduction in the threshold entanglement density owing to the longer length of the flexible polymeric backbone is crucial to impart low-temperature self-healing ability and stress-responsive properties to IHP.

Inverse Pickering emulsions stabilized by naturally derived particles are of interesting during the past decade. In this study, starch-based nanoparticles were used as a particulate emulsifier to stabilize a w/o Pickering emulsion. The effects of particle concentration and oil volume fraction on the emulsion type and stability were investigated in detail. Catastrophic phase inversion from o/w to w/o emulsions occurred at a volume fraction of oil of 0.3-0.4, without altering the particle wettability. Further, a linear relation existed between the average droplet diameter and total amounts of starch-based nanoparticles. The obtained starch-based nanoparticles also served as a Pickering stabilizer to conduct a w/o Pickering polymerization. Raspberry-like thermoresponsive starch-poly(N-isopropyl acrylamide) nanocomposites with a well-defined structure were synthesized.

Chemical modifications of histones can mediate diverse DNA-templated processes, including gene transcription1–3. Here we provide evidence for a class of histone post-translational modification, serotonylation of glutamine, which occurs at position 5 (Q5ser) on histone H3 in organisms that produce serotonin (also known as 5-hydroxytryptamine (5-HT)). We demonstrate that tissue transglutaminase 2 can serotonylate histone H3 tri-methylated lysine 4 (H3K4me3)-marked nucleosomes, resulting in the presence of combinatorial H3K4me3Q5ser in vivo. H3K4me3Q5ser displays a ubiquitous pattern of tissue expression in mammals, with enrichment observed in brain and gut, two organ systems responsible for the bulk of 5-HT production. Genome-wide analyses of human serotonergic neurons, developing mouse brain and cultured serotonergic cells indicate that H3K4me3Q5ser nucleosomes are enriched in euchromatin, are sensitive to cellular differentiation and correlate with permissive gene expression, phenomena that are linked to the potentiation of TFIID4–6 interactions with H3K4me3. Cells that ectopically express a H3 mutant that cannot be serotonylated display significantly altered expression of H3K4me3Q5ser-target loci, which leads to deficits in differentiation. Taken together, these data identify a direct role for 5-HT, independent from its contributions to neurotransmission and cellular signalling, in the mediation of permissive gene expression. In serotonin-rich tissues, tissue transglutaminase 2 is able to attach serotonin to a glutamine residue in histone H3; this modification mediates permissive gene expression in these tissues.

The effects of transient temperature variation of gain medium on quasi-three-level microchip laser were investigated. Firstly, the dynamic behavior with temperature variation and the characteristic of the output power were reported. The numerical simulation results revealed not only the dynamics characteristic of lasing levels, but also the relationship between pump pulse width and output power in equivalent duty cycle. The increments of output power deviated significantly from linear increasing with the pump pulse width. The characteristic of the output power with different duty cycle was compared. Because the heat load was rising with the increase of the duty cycle and high heat load reduced population inversion density, the optical-to-optical efficiency of 9.7% at 50% duty cycle was lower than optical-to-optical efficiency of 15.6% at 7% duty cycle. The calculated and experimental pump power thresholds for output of 1030 nm were discussed. Particularly, the output power calculated by the model with the addition of temperature terms was significantly lower than that simulated by the model without temperature terms. Experimental results have shown a good agreement with the theoretical predictions.

To investigate the short-term efficacy of laparoscopic radical resection for colorectal cancer with bowel obstruction and the effects of the surgery on inflammatory factors for improving the clinical treatment of the condition.The data of colorectal cancer patients presenting bowel obstruction (n = 167) treated at our hospital from January 2019 to December 2020 were assessed. The patients were divided into a laparoscopic radical resection of colorectal cancer group (LRRCC, n = 90) and open surgery group (OP, n = 77). Before treatment and on the 1st, 3rd, 5th, 7th and 15th day after treatment, their serum levels of pain factors, neuropeptide Y, prostaglandin E2 and nerve growth factor were measured by a serum biochemistry analyzer, their levels of inflammatory factors including C-reactive protein, interleukin 6 (IL-6), IL-8 and tumor necrosis factor-α by ELISA, and their amount of CD3+, CD4+ and CD8+ T cell subsets were measure by flow cytometry. Anorectal motility was assessed before and 4 and 8 weeks after treatment. Survival rates were assessed using the Kaplan-Meier method.On the 1st, 3rd, 5th, 7th and 15th day after treatment, compared with the OP group, the LRRCC group had lower levels of serum pain factors, inflammatory factors and CD8+T lymphocytes, while their numbers of CD3+ and CD4+ T lymphocytes subsets were significantly increased. Further, the LRRCC group had fewer complications and significantly higher survival rates, demonstrating better efficacy than the OP group.Laparoscopic radical resection was effective and achieved superior outcomes than open surgery in treating colorectal cancer patients with bowel obstruction.

Serotonylation of glutamine 5 on histone H3 (H3Q5ser) was recently identified as a permissive posttranslational modification that coexists with adjacent lysine 4 trimethylation (H3K4me3). While the resulting dual modification, H3K4me3Q5ser, is enriched at regions of active gene expression in serotonergic neurons, the molecular outcome underlying H3K4me3-H3Q5ser crosstalk remains largely unexplored. Herein, we examine the impact of H3Q5ser on the readers, writers, and erasers of H3K4me3. All tested H3K4me3 readers retain binding to the H3K4me3Q5ser dual modification. Of note, the PHD finger of TAF3 favors H3K4me3Q5ser, and this binding preference is dependent on the Q5ser modification regardless of H3K4 methylation states. While the activity of the H3K4 methyltransferase, MLL1, is unaffected by H3Q5ser, the corresponding H3K4me3/2 erasers, KDM5B/C and LSD1, are profoundly inhibited by the presence of the mark. Collectively, this work suggests that adjacent H3Q5ser potentiates H3K4me3 function by either stabilizing H3K4me3 from dynamic turnover or enhancing its physical readout by downstream effectors, thereby potentially providing a mechanism for fine-tuning critical gene expression programs.

Ni-rich LiNi

A key challenge in trace heavy metals removal from drinking water by adsorption technology is to achieve high adsorption capacity and rapid uptake speed of adsorbent. Herein, we report a functionalized double modified covalent organic framework (DMTD-COF-SH) bearing high-density sulfur and nitrogen chelating groups provided simultaneously by 2,5-dimercapto-1,3,4-thiadiazole (DMTD) and 1,2-ethanedithiol, which was prepared via a facile one-pot thiol-ene "click" reaction. PXRD, FTIR, XPS, SEM, BET and

Heterochromatin Protein 1 (HP1) recognizes histone H3 lysine 9 methylation (H3K9me) through its conserved chromodomain and maintains heterochromatin from fission yeast to mammals. However, in Arabidopsis, Like Heterochromatin Protein 1 (LHP1) recognizes and colocalizes genome-wide with H3K27me3, and is the functional homolog of Polycomb protein. This raises the question whether genuine HP1 homologs exist in plants. Here, we report on the discovery of ADCP1, a plant-specific triple tandem Agenet protein, as a multivalent H3K9me reader in Arabidopsis, and establish that ADCP1 is essential for heterochromatin formation and transposon silencing through modulating H3K9 and DNA methylation levels. Structural studies revealed the molecular basis underlying H3K9me-specific recognition by tandem Agenet of ADCP1. Similar to human HP1α and fly HP1a, ADCP1 mediates heterochromatin phase separation. Our results demonstrate that despite its distinct domain compositions, ADCP1 convergently evolves as an HP1-equivalent protein in plants to regulate heterochromatin formation.

Histone post-translational modifications (PTMs) and their recognition by histone readers exert crucial functions in eukaryotes. Despite extensive studies, conservation and diversity of histone PTM regulation between animals and plants remain less explored because of a lack of systematic knowledge of histone readers in plants. Based on a high-throughput surface plasmon resonance imaging (SPRi) platform, we report the lab-on-chip profiling of interactions between 204 putative reader domains and 11 types of histone peptides in Arabidopsis thaliana. Eleven reader hits were then chosen for histone combinatorial readout pattern profiling. Systematic analysis of histone PTM recognition in Arabidopsis thaliana reveals that plant and human histone readers share conservation in domain types and recognition mechanisms. The differences in particular histone mark recognition by transcription regulator EML1 and DNA damage repair factor MSH6 indicate plant-specific histone PTMs function in Arabidopsis thaliana acquired during evolution.

A green strategy is designed for synthesizing LiMn0.8Fe0.2PO4/C composites bases on mechano-chemical liquid-phase activation technique. The micro-nano spherical precursor is prepared by the effective redox reaction between MnO2 and H2O2 in H3PO4 aqueous solution with subsequent addition FeC2O4•2H2O and Li2CO3, which is followed by spray drying. The dense LiMn0.8Fe0.2PO4/C microspheres are formed from conformal carbon coating connected with primary nano-sized particles, which provides rapid electron and ion transport pathways during the electrode reaction. The obtained LiMn0.8Fe0.2PO4/C cathode exhibits reduced electrochemical polarization with high voltage platform and high discharge capacity of 159 mAh g −1 at 0.1 C. Even at high rate of 10 C, the composite shows an impressing discharge capacity of 130 mAh g −1 with obviously stable plateau. Besides, uniformly conductive carbon network distributed all over the primary nano-sized particles effectively inhibits the occurrence of interfacial side reactions during electrode cycling, and the electrode exhibits good cycling stability with capacity retention rate of 95% after 500 cycles at 1 C. This work provides a scalable route to fabricate high energy density LiMn0.8Fe0.2PO4/C cathode with excellent rate performance for Li-ion battery.

To overcome the adverse effects of salt on the mechanical properties of hydrogels, a facile double cross-linking method has been proposed to synthesize salt-enhanced tough hydrogels. Herein, a poly(hexafluorobutyl methacrylate-acrylamide) hydrogel [P(AAm-co-HFBMA) hydrogel] is prepared by the copolymerization of acrylamide (AAm) and hexafluorobutyl methacrylate (HFBMA) with N,N'-methylene bisacrylamide (NMBA) as a cross-linking agent in a dimethylformamide (DMF)/aqueous solution; DMF is then replaced by water. The results indicate that the tensile fracture stress of the P(AAm-co-HFBMA) hydrogel (20 mol% HFBMA) is as high as 0.43 MPa, which is far better than that of the PAAm hydrogel (ca. 30 kPa). Additionally, with a further increase in the hydrophobic structural units (25 mol% HFBMA), the tensile fracture stress of the P(AAm-co-HFBMA) hydrogel can be increased up to 2.34 MPa. The mechanical strength of the P(AAm-co-HFBMA) hydrogel is significantly enhanced to 3.50 MPa (2 M) from 2.34 MPa (0 M) after it is soaked in aqueous NaCl solutions with various salt concentrations. The mechanical properties and the results of the DSC analysis indicate that the main reason for its mechanical strength to exhibit a unique salt-enhancement trend can be explained as follows. After the P(AAm-co-HFBMA) hydrogel is soaked in the salt solution, the network gradually collapses with the penetration of the small molecules of salt. Thus, the hydrophobic C-F units easily form dynamic cross-linking junctions due to the switchable hydrophobic interaction between C-F groups, which can endow the P(AAm-co-HFBMA) hydrogel with a more effective dynamic energy dissipation mechanism in salt solution.

We study biosourced core-shell particles with a starch-based core and thermo-responsive polymer brush shell using surface-initiated single-electron transfer living radical polymerization (SI-SET-LRP) as a Pickering stabilizer. The shell endows the Pickering stabilizer with reversible emulsification/demulsification of oil and water properties. The initiator attached to the starch-based nanosphere (Br-SNP) core particle was first fabricated using the precipitation method. Subsequently, dense poly( N-isopropylacrylamide) (PNIPAM) brush graft-modified starch-based nanoparticles (SNP- g-PNIPAM) were obtained via the SI-SET-LRP process. Interfacial properties of the resultant particles were analyzed by interfacial tensiometer measurements, as were the effects of the grafted polymer chain length and temperature on the interfacial activity. Pickering emulsion was obtained using SNP- g-PNIPAM particles as the stabilizer. The effect of the concentration of the Pickering stabilizer on the size of emulsion droplets was analyzed. The emulsification/demulsification process of the Pickering emulsion can be reversed and easily repeated by changing the temperature.

We have demonstrated a high peak power electro-optically cavity-dumped (CD) laser and a high energy picosecond regenerative amplifier (RGA) at 1342 nm. Their output power, pulse energy, pulse widths, and peak power were reported, respectively. For CD operation, the maximum pulse energy was 0.308 mJ at 1 kHz with the pulse width of 23.3 ns. The corresponding peak power was 13.2 kW. The maximum pulse energy of 0.243 mJ was extracted from RGA at 1 kHz under the seeded pulse energy of 250 pJ, resulting in its total optical gain of 9.7×105 . Its pulse width was estimated to be 43.8 ps, corresponding to a peak power of 5.55 MW.

Highly doped erbium crystals have complex fine energy levels, which can be used to emit lasers of different wavelengths under different conditions. The mid-infrared multi-wavelength laser of erbium ions has not yet achieved stable laser emission. In this study, the rate equation is used, with consideration of mode competition, to design a mid-infrared Er:YAG pulsed laser that emits four wavelengths at room temperature. The gain of the multi-wavelength erbium laser is related to the Boltzmann distribution coefficient. Based on this, the conditions for multi-wavelength output have been calculated and verified in experiments. A four-wavelength stable output mid-infrared pulsed laser based on Er:YAG was produced. This laser may be applied to remote sensing or gas detection.

A novel eco-friendly synthesis of LiFe0.25Mn0.75PO4/C@ reduced graphene oxide (rGO) was carried out. The effects of different grinding-drying process and reduced graphene oxide (rGO) modification on the morphology and electrochemical performance of the synthesized LiFe0.25Mn0.75PO4 materials were studied in detail. The studies show that the sanding assistant spray drying process can effectively refine the particle size of LiFe0.25Mn0.75PO4/C materials with uniform dispersion. The uniform nano size combination of rGO and carbon coating significantly reduce the charge-transfer impedance of electrode materials, and improve the conductivity and electrochemical properties of the materials. The optimization results show that LiFe0.25Mn0.75PO4/C@rGO materials display the most favorable kinetic behavior and the best electrochemical reversibility, with the specific discharge capacity of 143.8, and 139.8 mAh g−1 at 1 C and 2 C. After 100 cycles at 1 C, the capacity retention maintains 97.64%, showing a promising application prospect for lithium-ion batteries.

Conventional approaches to generating double emulsions are cumbersome, complicated, and based on a two-step emulsification process using a combination of two distinctive surfactants. In this work, the surface properties of diatomite particles were successfully tailored by chemical modification with palmitoyl chloride. The properties of the resulting diatomite particles changed from the original hydrophilicity to hydrophobicity, leading to straightforward stabilization of oil-in-water-in-oil (O/W/O) Pickering double emulsions by a one-step emulsification process. Pickering double high internal phase emulsions (HIPEs) with an internal phase up to 80 vol% could be produced solely using the modified diatomite particles. The water-in-oil (W/O) droplet sizes of these HIPEs were much larger than the droplets of conventional nanoparticle-stabilized Pickering HIPEs. Furthermore, using the O/W/O Pickering double emulsions as templates, the porous polymer particles were fabricated. In addition, it was demonstrated that the wide particle size distribution of diatomite particles and modified heterogeneity were the reasons for the formation of multiple emulsions.

Colorectal cancer (CRC) is one of the most common malignancies worldwide. However, therapies against CRC have not been completely effective. Astragaloside IV (AS-IV) has shown anti-tumorigenic properties in certain cancers, but its role in CRC remains unclear. In this study, we investigated the therapeutic effect of AS-IV in CRC and explored its underlying mechanism. The results showed that AS-IV dose-dependently inhibited the proliferation of CRC cells and suppressed tumor growth in CRC xenograft mouse models. In addition, AS-IV promoted cell cycle arrest in the G0 phase, associated with increased expression of p21. Furthermore, flow cytometry demonstrated that AS-IV promoted apoptosis of CRC cells in a dose-dependent manner. AS-IV induced caspase-dependent apoptosis, which involved the increased release of cytochrome c and Omi from the mitochondria into the cytoplasm and the up-regulation of Bax/Bcl-2 ratio, as well as the activation of PARP and caspase cascade (caspase-3 and -9). Taken together, our study has identified a novel function of AS-IV and provided a molecular basis for AS-IV's potential applications in the treatment of CRC and other cancers.

In this work, the anisotropy of nonlinear absorption in a crystal Q-switch was considered when we established coupled rate equations of a passively Q-switched laser. A [100]-cut Cr

Resveratrol, a natural product, has been revealed to exert antitumor effects in multiple types of tumors. However, the antitumor effects of resveratrol on hepatocellular carcinoma (HCC) and its potential underlying mechanisms have not yet been elucidated. The present study demonstrated that resveratrol inhibited viability, proliferation, invasion and migration of HCC cells significantly in a time‑ and dose‑dependent manner, indicating that resveratrol exerted antitumor effects in HCC. Furthermore, relative expression of autophagy‑related proteins Beclin1 and LC3 II/I ratio was increased while p62 expression was decreased by resveratrol treatment dose‑dependently. The LC3+ puncta formation, which represented autophagosome formation was also markedly dose‑dependently upregulated by resveratrol treatment, suggesting that resveratrol induced autophagy in HCC cells. In addition, treatment with autophagy inhibitor 3‑methyladenine (3‑MA) counteracted the inhibitory effect of resveratrol on HCC cell proliferation, invasion and migration, indicating that suppressing autophagy may hamper the antitumor effect of resveratrol in HCC. It was revealed that resveratrol upregulated the expression of p53 while decreasing the ratio of phosphorylated protein kinase B (p‑Akt)/Akt in HCC cells. Treatment with p53 inhibitor pifithrin‑α and Akt activator insulin‑like growth factor‑1 decreased the expression of Beclin1 while significantly promoting cell proliferation, invasion and migration compared with the resveratrol treatment group. Taken together, the results of the present study revealed that resveratrol inhibited the proliferation and mobility of HCC cells through inducing autophagy via activating p53 and inhibiting phosphoinositide 3‑kinase/Akt. Enhancing autophagy can augment the antitumor effects of resveratrol in HCC. Therefore, combining resveratrol with an autophagy inducer may be a viable option for treating HCC.

Chemical modifications on histones and DNA/RNA constitute a fundamental mechanism for epigenetic regulation. These modifications often function as docking marks to recruit or stabilize cognate “reader” proteins. So far, a platform for quantitative and high-throughput profiling of the epigenetic interactome is urgently needed but still lacking. Here, we report a 3D-carbene chip-based surface plasmon resonance imaging (SPRi) technology for this purpose. The 3D-carbene chip is suitable for immobilizing versatile biomolecules (e.g., peptides, antibody, DNA/RNA) and features low nonspecific binding, random yet function-retaining immobilization, and robustness for reuses. We systematically profiled binding kinetics of 1,000 histone “reader–mark” pairs on a single 3D-carbene chip and validated two recognition events by calorimetric and structural studies. Notably, a discovery on H3K4me3 recognition by the DNA mismatch repair protein MSH6 in Capsella rubella suggests a mechanism of H3K4me3-mediated DNA damage repair in plant.

We have established a new method for realizing a typical “2-color” collinear CARS (coherent anti-Stokes Raman scattering) system. The system mainly consists of a laser source, a D2O cell, and a spectrometer. The pump/probe beam and the Stokes beam are provided by SBS (stimulated Brillouin scattering) and BSRS (backward stimulated Raman scattering) of D2O, respectively. The CARS system is statistically stable, and it is also a broadband and alignment-free system. Measurement of N2 signal in air with this system is demonstrated. Detection of N2 in 0.006 bar air is realized with this system. Time-resolved pulse shapes of SBS and BSRS are measured to confirm their generation. Transference of energy from the SBS pulse to the BSRS pulse is realized with a Rhodamine 101 dye cuvette and discussed. This results in a better energy distribution between the pump/probe and Stokes pulses for CARS.

In this work, a passively Q-switched Nd:YAG laser resonator, with an output coupling of more than 90 % , was demonstrated. Laser pulse energy, peak power and pulse width were found to increase with the increasing of dissipative loss of the laser resonator, and pulse energy was found to increase from 38.6 mJ to 113 mJ, which almost meant a 200 % increase. However, according to previous theoretical analyses of passively Q-switched lasers, pulse energy and peak power would decrease with the increasing of dissipative loss when the second threshold was satisfied, and a giant Q-switched laser pulse would never occur if the second threshold was not satisfied. For the passively Q-switched laser resonator we established, the second threshold was found not to be satisfied because of the high output coupling. So, we modified the solutions of coupled rate equations when the second threshold was not satisfied. Numerical calculation results were carried out, and these calculation results were basically consistent with the experimental results and previous investigations.