An e-Xist-ential two-edged sword for women.

Xist-containing ribonucleoproteins drive autoimmunity in women.

Rapid Volumetric Bioprinting of Decellularized Extracellular Matrix Bioinks.

Decellularized extracellular matrix (dECM)-based hydrogels are widely applied to additive biomanufacturing strategies for relevant applications. The extracellular matrix components and growth factors of dECM play crucial roles in cell adhesion, growth, and differentiation. However, the generally poor mechanical properties and printability have remained as major limitations for dECM-based materials. In this study, heart-derived dECM (h-dECM) and meniscus-derived dECM (Ms-dECM) bioinks in their pristine, unmodified state supplemented with the photoinitiator system of tris(2,2-bipyridyl) dichlororuthenium(II) hexahydrate and sodium persulfate, demonstrate cytocompatibility with volumetric bioprinting processes. This recently developed bioprinting modality illuminates a dynamically evolving light pattern into a rotating volume of the bioink, and thus decouples the requirement of mechanical strengths of bioprinted hydrogel constructs with printability, allowing for the fabrication of sophisticated shapes and architectures with low-concentration dECM materials that set within tens of seconds. As exemplary applications, cardiac tissues are volumetrically bioprinted using the cardiomyocyte-laden h-dECM bioink showing favorable cell proliferation, expansion, spreading, biomarker expressions, and synchronized contractions; whereas the volumetrically bioprinted Ms-dECM meniscus structures embedded with human mesenchymal stem cells present appropriate chondrogenic differentiation outcomes. This study supplies expanded bioink libraries for volumetric bioprinting and broadens utilities of dECM toward tissue engineering and regenerative medicine.

Insights into adsorption behavior and mechanism of Cu(II) onto biodegradable and conventional microplastics: Effect of aging process and environmental factors.

The widespread promotion attempt of biodegradable plastics is considered as an effective solution to address conventional plastic pollution. However, the interaction of microplastics (MPs) easily broken down from biodegradable plastics with the coexisting pollutants in aquatic environments has gained less attention. Herein, we investigated the effects of the aging process and environmental factors on copper (Cu(II)) adsorption behavior by biodegradable polylactic acid and conventional polystyrene MPs. Results demonstrated that the aging process significantly altered physicochemical properties of both types of MPs, and PLA showed less resistance to aging. The aged polylactic acid MPs (aged-PLA) exhibited the far highest Cu(II) maximum adsorption capacity (7.13 mg/g) mainly due to its abundant oxygen-containing functional groups (OCFGs), followed by pristine polylactic acid (PLA, 6.08 mg/g), aged polystyrene (aged-PS, 0.489 mg/g) and pristine polystyrene (PS, 0.365 mg/g). The adsorption kinetics of Cu(II) on PLA MPs were controlled by film and intraparticle diffusion, while film diffusion governed the Cu(II) adsorption onto PS MPs. In addition to roles of rougher surface structure, greater surface area and pore filling, the complexation of OCFGs and electrostatic interaction were critical to the adsorption mechanism of aged-PLA and aged-PS, and cation-π interaction was associated with adsorption of aged-PS. Moreover, the adsorption capacity of Cu(II) on aged MPs gradually grew with the increasing pH from 4 to 7. Besides, humic acid significantly promoted the adsorption of Cu(II) at a low concentration (0-20 mg/L) due to the formation of binary mixtures of MPs-HA but inhibited the adsorption at a high concentration (50 mg/L) because of its competitive effect, suggesting the dual roles of humic acid in the adsorption process. Overall, our findings provide a better understanding of the adsorption behavior of metals on biodegradable MPs and emphasize their non-negligible risk as carriers of contaminant.

Bi3O4Cl/g-C3N4/Cd0.5Zn0.5S Double Z-Scheme Heterojunction Photocatalyst for Highly Selective CO2 Reduction to Methane.

Solar-energy-driven CO2 hydrogenation is a promising strategy to alleviate the climate crisis. Methane is a desirable derivative of CO2 reduction. However, developing a photocatalyst for highly active and selective CH4 generation remains challenging. Herein, we report a double Z-scheme Bi3O4Cl/g-C3N4/Cd0.5Zn0.5S photocatalyst for efficient reduction of CO2 to CH4. In situ characterization techniques confirmed that the charge migration mechanism in Bi3O4Cl/g-C3N4/Cd0.5Zn0.5S promotes charge separation through double internal electric fields. As a result, the optimized C0.01B0.02C catalyst displayed a formation rate high up to 25.34 µmol g-1 h-1 and a selectivity of 96.52% of CH4. Moreover, the AQY of CO2 conversion on C0.01B0.02C (1.84%) was almost 41 times higher than that of the bare CN. This study provides a novel perspective to develop heterojunction photocatalysts for selective CO2 conversion to CH4.

Comparative Transcriptome Analysis of Acne vulgaris, Rosacea, and Hidradenitis Suppurativa Supports High Dose Dietary Zinc as a Therapeutic Agent.

Acne vulgaris, rosacea, and hidradenitis suppurativa are enduring inflammatory skin conditions that frequently manifest with akin clinical attributes, posing a considerable challenge for their distinctive diagnosis. While these conditions do exhibit certain resemblances, they also demonstrate distinct underlying pathophysiological mechanisms and treatment modalities. Delving into both the molecular parallels and disparities among these three disorders can yield invaluable insights for refined diagnostics, effective management, and targeted therapeutic interventions. In this report, we present a comparative analysis of transcriptomic data across these three diseases, elucidating differentially expressed genes and enriched pathways specific to each ailment, as well as those shared among them. We also identified high dose dietary zinc as a potential therapeutic agent and validated its efficacy in an acne mouse model.

Satellite-Based On-Orbit Printing of 3D Tumor Models.

Space three dimension (3D） bioprinting provides a precise and bionic tumor model for evaluating the compound effect of the space environment on tumors, thereby providing insight into the progress of the disease and potential treatments. However, space 3D bioprinting faces several challenges, including prelaunch uncertainty, possible liquid leakage, long-term culture in space, automatic equipment control, data acquisition, and transmission. Here, a novel satellite-based 3D bioprinting device with high structural strength, small volume, and low weight (<6 kg) is developed. A microgel-based biphasic thermosensitive bioink and suspension medium that supports the on-orbit printing and in situ culture of complex tumor models is developed. An intelligent control algorithm that enables the automatic control of 3D printing, autofocusing, fluorescence imaging, and data transfer back to the ground is developed. To the authors' knowledge, this is the first time that on-orbit printing of tumor models is achieved in space with stable morphology and moderate viability via a satellite. It is found that 3D tumor models are more sensitive to antitumor drugs in space than on Earth. This study opens up a new avenue for 3D bioprinting in space and offers new possibilities for future research in space life science and medicine.

A dual Z-scheme heterojunction Cu-CuTCPP/Cu2O/CoAl-LDH for photocatalytic CO2 reduction to C1 and C2 products.

In this research, a ternary Cu-CuTCPP/Cu2O/CoAl-LDH composite with a dual Z-scheme heterostructure was fabricated based on a Cu2O photocatalyst and applied in photocatalytic CO2 reduction. The physicochemical properties of the prepared catalysts and the possible reaction mechanism in CO2 reduction were analyzed and studied by various characterization methods. The activity of CO2 reduction significantly increased, especially forming C2 products. The optimal yield of C2H4 and C2H6 reached 1.56 and 1.92 µmol g-1 h-1 respectively, which was 14.45 and 17.45 times that from using the Cu2O monomer. In addition, the selectivity of C2 products reached 37.4%. The satisfactory C2 yield was mainly due to the fact that Cu1+δ2(COO)3 nodes in Cu-CuTCPP contained adjacent Cu sites, which effectively promoted the C-C coupling reaction. Moreover, the dual Z-scheme heterojunction stimulated the separation of photogenerated electron-hole pairs and diminished the recombination rate. This work contributes to the development of novel photocatalysts with a dual Z-scheme heterojunction and facilitates the generation of valuable C2 products.

Recent Progress of Covalent Organic Frameworks-Based Materials in Photocatalytic Applications: A Review.

Covalent organic frameworks (COFs) are one type of porous organic materials linked by covalent bonds. COFs materials exhibit many outstanding characteristics such as high porosity, high chemical and thermal stability, large specific surface area, efficient electron transfer efficiency, and the ability for predesigned structures. These exceptional advantages enable COFs materials to exhibit remarkable performance in photocatalysis. Additionally, the activity of COFs materials as photocatalysts can be significantly upgraded by ion doping and the formation of heterojunctions. This paper summarizes the latest research progress on COF-based materials applied in photocatalytic systems. Initially, typical structures and preparation methods of COFs are analyzed and compared. Moreover, the essential principles of photocatalytic reactions over COFs-based materials and the latest research developments in photocatalytic hydrogen production, CO2 reduction, pollutants elimination, organic transformation, and overall water splitting are indicated. At last, the outlook and challenges of COF-based materials in photocatalysis are discussed. This review is intended to permit instructive guidance for the efficient use of photocatalysis based on COFs in the future.

Constructing CoAl-LDO/MoO3-x S-scheme heterojunctions for enhanced photocatalytic CO2 reduction.

Converting CO2 into chemicals and fuels by solar energy can alleviate global warming and solve the energy crisis. In this work, CoAl-LDO/MoO3-x (LDO/MO) composites were successfully prepared and achieved efficient CO2 reduction under visible light. The CoAl-layered double oxides (CoAl-LDO) evolved from CoAl-layered double hydroxide (CoAl-LDH) exhibited a more robust structure, broader light absorption, and improved CO2 adsorption ability. The local surface plasmon resonance (LSPR) effect excited by nonstoichiometric MoO3-x broadened the photo-response range of CoAl-LDO/MoO3-x. In addition, constructing step-scheme (S-scheme) heterojunctions could simultaneously optimize the migration mechanism of photogenerated electrons and holes, and retain carriers with strong redox ability. Therefore, the production rates of CO and CH4 on the optimal LDO/MO composite were 7 and 9 times higher than the pristine CoAl-LDH, respectively. This work hybridizes oxidation photocatalysts and LDO-based materials to optimize the charge separation and migration mechanisms, which guides the modification of LDO-based materials.

Recent progress of cocatalysts loaded on carbon nitride for selective photoreduction of CO2 to CH4.

A photocatalytic system driven by solar light is one of the promising strategies for converting CO2 into valuable energy. The reduction of CO2 to CH4 is widely studied since CH4 has a high energy density as the main component of nonrenewable natural gas. Therefore, it is necessary to develop semiconductor materials with high photocatalytic activity and CH4 selectivity. Graphitic carbon nitride (g-C3N4/CN) has attracted widespread attention for photocatalytic CO2 reduction due to its excellent redox ability and visible light response. A hybrid system constructed by loading cocatalysts on g-C3N4 can significantly improve the yield of target products, and serve as a general platform to explore the mechanism of the CO2 reduction reaction. Herein, we briefly introduce the theory of selective CO2 photoreduction and the basic properties of cocatalysts. Then, several typical configurations and modification strategies of cocatalyst/CN systems for promoting CH4 selective production are presented in detail. In particular, we systematically summarize the application of cocatalyst/CN composite photocatalysts in the selective reduction of CO2 to methane, according to the classification of cocatalysts (monometal, bimetal, metal-based compound, and nanocarbon materials). Finally, the challenges and perspectives for developing cocatalyst/g-C3N4 systems with high CH4 selectivity are presented to guide the rational design of catalysts with high performance in the future.

Research Progress on Photocatalytic CO2 Reduction Based on Perovskite Oxides.

Photocatalytic CO2 reduction to valuable fuels is a promising way to alleviate anthropogenic CO2 emissions and energy crises. Perovskite oxides have attracted widespread attention as photocatalysts for CO2 reduction by virtue of their high catalytic activity, compositional flexibility, bandgap adjustability, and good stability. In this review, the basic theory of photocatalysis and the mechanism of CO2 reduction over perovskite oxide are first introduced. Then, perovskite oxides' structures, properties, and preparations are presented. In detail, the research progress on perovskite oxides for photocatalytic CO2 reduction is discussed from five aspects: as a photocatalyst in its own right, metal cation doping at A and B sites of perovskite oxides, anion doping at O sites of perovskite oxides and oxygen vacancies, loading cocatalyst on perovskite oxides, and constructing heterojunction with other semiconductors. Finally, the development prospects of perovskite oxides for photocatalytic CO2 reduction are put forward. This article should serve as a useful guide for creating perovskite oxide-based photocatalysts that are more effective and reasonable.

Fabrication and characterization of Z-scheme BiOCl/C/Cu2O heterojunction nanocomposites as efficient catalysts for the photocatalytic reduction of CO2.

The photocatalytic reduction of CO2 to hydrocarbons is expected to simultaneously alleviate the energy crisis and greenhouse effect. Herein, the ternary BiOCl/C/Cu2O catalysts with different mass ratios were compounded using a simple hydrothermal method, revealing better photocatalytic activity than the monomer. In the absence of sacrificial agents and photosensitizers, 25% BiOCl/C/Cu2O showed optimal photocatalytic performance. The CO and CH4 yields over 25% BiOCl/C/Cu2O reached 26.77 and 9.86 µmol g-1 h-1, which is 2.9 and 8.7 times higher than that of the pristine Cu2O, respectively. The ameliorative activity can be attributed to the construction of the Z-scheme heterostructure and carbon layer, which are conducive to the transfer and separation of photogenerated carriers. This study offers valuable references for the design and investigation of a Z-scheme heterojunction using a carbon layer as an electron transfer medium.

Recent Progress of Single-Atom Photocatalysts Applied in Energy Conversion and Environmental Protection.

Photocatalysis driven by solar energy is a feasible strategy to alleviate energy crises and environmental problems. In recent years, significant progress has been made in developing advanced photocatalysts for efficient solar-to-chemical energy conversion. Single-atom catalysts have the advantages of highly dispersed active sites, maximum atomic utilization, unique coordination environment, and electronic structure, which have become a research hotspot in heterogeneous photocatalysis. This paper introduces the potential supports, preparation, and characterization methods of single-atom photocatalysts in detail. Subsequently, the fascinating effects of single-atom photocatalysts on three critical steps of photocatalysis (the absorption of incident light to produce electron-hole pairs, carrier separation and migration, and interface reactions) are analyzed. At the same time, the applications of single-atom photocatalysts in energy conversion and environmental protection (CO2 reduction, water splitting, N2 fixation, organic macromolecule reforming, air pollutant removal, and water pollutant degradation) are systematically summarized. Finally, the opportunities and challenges of single-atom catalysts in heterogeneous photocatalysis are discussed. It is hoped that this work can provide insights into the design, synthesis, and application of single-atom photocatalysts and promote the development of high-performance photocatalytic systems.

Electrical Stimulation Promotes the Vascularization and Functionalization of an Engineered Biomimetic Human Cardiac Tissue.

The formation of multiscale vascular networks is essential for the in vitro construction of large-scale biomimetic cardiac tissues/organs. Although a variety of bioprinting processes have been developed to achieve the construction of mesoscale and large-scale blood vessels, the formation of microvascular networks still mainly depends on the self-assembly behavior of endothelial cells (ECs), which is inefficient and demanding without appropriate stimulus. To address this problem, the elongation and connection of endothelial cells in engineered cardiac tissue (ECT) are sought to promote by electrical stimulation (ES) to achieve vascularization. As proof of the concept, bio-inks are composed of GelMA/fibrin hydrogel, human pluripotent stem cells induced cardiomyocytes (iPSC-CM), and human umbilical vein endothelial cells (HUVEC) are used for the bioprinting of ECTs. It is demonstrated that electrical stimulation significantly promotes the elongation, migration, and interconnection of HUVECs in ECT and increases the expression of related genes. Moreover, ES also enhances the secretion of signal factors interacting between CMs and HUVECs. It seems that the HUVECs further strengthen the contractility of cardiac tissue. Taken together, electrical stimulation promotes vascularization and CMs functionalization in ECT, which has important application potential in the fabrication of vascularized ECT and its clinical transplantation.

Liquid-embedded (bio)printing of alginate-free, standalone, ultrafine, and ultrathin-walled cannular structures.

While there has been considerable success in the three-dimensional bioprinting of relatively large standalone filamentous tissues, the fabrication of solid fibers with ultrafine diameters or those cannular featuring ultrathin walls remains a particular challenge. Here, an enabling strategy for (bio)printing of solid and hollow fibers whose size ranges could be facilely adjusted across a broad spectrum, is reported, using an aqueous two-phase embedded (bio)printing approach combined with specially designed cross-linking and extrusion methods. The generation of standalone, alginate-free aqueous architectures using this aqueous two-phase strategy allowed freeform patterning of aqueous bioinks, such as those composed of gelatin methacryloyl, within the immiscible aqueous support bath of poly(ethylene oxide). Our (bio)printing strategy revealed the fabrication of standalone solid or cannular structures with diameters as small as approximately 3 or 40 µm, respectively, and wall thicknesses of hollow conduits down to as thin as <5 µm. With cellular functions also demonstrated, we anticipate the methodology to serve as a platform that may satisfy the needs for the different types of potential biomedical and other applications in the future, especially those pertaining to cannular tissues of ultrasmall diameters and ultrathin walls used toward regenerative medicine and tissue model engineering.

Converting CO2 into Value-Added Products by Cu2 O-Based Catalysts: From Photocatalysis, Electrocatalysis to Photoelectrocatalysis.

Converting CO2 into value-added products by photocatalysis, electrocatalysis, and photoelectrocatalysis is a promising method to alleviate the global environmental problems and energy crisis. Among the semiconductor materials applied in CO2 catalytic reduction, Cu2 O has the advantages of abundant reserves, low price and environmental friendliness. Moreover, Cu2 O has unique adsorption and activation properties for CO2 , which is conducive to the generation of C2+ products through CC coupling. This review introduces the basic principles of CO2 reduction and summarizes the pathways for the generation of C1 , C2 , and C2+ products. The factors affecting CO2 reduction performance are further discussed from the perspective of the reaction environment, medium, and novel reactor design. Then, the properties of Cu2 O-based catalysts in CO2 reduction are summarized and several optimization strategies to enhance their stability and redox capacity are discussed. Subsequently, the application of Cu2 O-based catalysts in photocatalytic, electrocatalytic, and photoelectrocatalytic CO2 reduction is described. Finally, the opportunities, challenges and several research directions of Cu2 O-based catalysts in the field of CO2 catalytic reduction are presented, which is guidance for its wide application in the energy and environmental fields is provided.

Volumetric additive manufacturing of pristine silk-based (bio)inks.

Volumetric additive manufacturing (VAM) enables fast photopolymerization of three-dimensional constructs by illuminating dynamically evolving light patterns in the entire build volume. However, the lack of bioinks suitable for VAM is a critical limitation. This study reports rapid volumetric (bio)printing of pristine, unmodified silk-based (silk sericin (SS) and silk fibroin (SF)) (bio)inks to form sophisticated shapes and architectures. Of interest, combined with post-fabrication processing, the (bio)printed SS constructs reveal properties including reversible as well as repeated shrinkage and expansion, or shape-memory; whereas the (bio)printed SF constructs exhibit tunable mechanical performances ranging from a few hundred Pa to hundreds of MPa. Both types of silk-based (bio)inks are cytocompatible. This work supplies expanded bioink libraries for VAM and provides a path forward for rapid volumetric manufacturing of silk constructs, towards broadened biomedical applications.

Differences in structure and composition of soil humic substances and their binding for polycyclic aromatic hydrocarbons in different climatic zones.

Humic substances (HSs) play important roles in the transport and bioavailability of hydrophobic organic compounds (HOCs) in soils. The sorption of HOCs depends on the compositions and structures of HSs which may differ in different climatic zones, however, the sorption behavior of HOCs by HSs in soils from different climatic zones is poorly understood. In this study, different HS fractions (humic acids-HAs, fulvic acids-FAs and humin-HM) in soils from different climatic zones were extracted and used as sorbents for polycyclic aromatic hydrocarbons (PAHs). The results indicated that HSs (including HA, FA and HM fractions) from colder climatic zones contained more oxygen-containing functional groups and exhibited smaller molecular weight as well as higher aliphaticity and polarity than those from warmer climatic zones. The sorption affinity of HAs at the low given concentration (0.05 Sw) of naphthalene (Nap), phenanthrene (Phe), pyrene (Pyr) and benz(α)anthracene (BaA) from warmer climatic zones to colder ones increased from 26.3 to 43.9, from 36.7 to 114.0, from 125.8 to 388.8, and from 322.5 to 876.1, respectively, and the same trends were obtained for FAs and HM at the same PAH concentration. The results indicated that HSs from colder climatic zones showed higher sorption affinity than those from warmer climatic zones. Moreover, the weighted contributions of FAs, HAs and HM to the overall sorption from different climatic zones were 9.1-28.4%, 13.5-59.2% and 23.4-76.9%, respectively. This indicates FA fraction, a previously neglected component, is also an important contributor to binding PAHs in soils. This study suggests that the difference in sorption behaviors of HOCs to HSs among different climatic zones should be considered when predicting HOC fates and bioavailability in soils.

Urban development enhances soil organic carbon storage through increasing urban vegetation.

Anthropogenic activities can lead to the loss of soil organic carbon (SOC) or improve its storage, hence they have the potential to exacerbate or help mitigate climate change. Urban expansion results in an initial loss of soil carbon, but long-term SOC changes during urban development are poorly understood. Herein, we studied SOC changes in the suburban and urban areas of cities with high levels of urbanization based on a long-term resampling campaign in Beijing, and a compilation of SOC content data from 21 other cities with high levels of urbanization across China over the past three decades. Our results revealed that the SOC of topsoils decreased by 17.2% in the suburban areas and increased by 104.4% in the urban areas of cities with high levels of urbanization. The changes in SOC were positively correlated with the changes in vegetation coverage and productivity. Partial least square method structural equation model analyses showed that changes in vegetation could directly affect SOC changes, and the changes in vegetation coverage and productivity were induced by human activities and climate changes in Beijing. The topsoils in the urban areas of cities with high levels of urbanization can act as carbon sinks due to the increase in vegetation. This study can help improve our understanding of the role of the SOC content of cities within the global C cycle and provide suggestions for achieving the goal of carbon neutrality in China.

Warming-induced greenhouse gas fluxes from global croplands modified by agricultural practices: A meta-analysis.

Climate warming increases the emissions of soil greenhouse gases (GHGs) by stimulating carbon (C) and nitrogen (N) processes in terrestrial ecosystems, contributing to climate change. However, the responses of soil GHG fluxes to warming from global agricultural ecosystems remain unknown. Here, we evaluate the effects of warming on soil GHG fluxes from global croplands under different agro-ecosystems, cropping systems, crop species, and N fertilizer levels, and determine the potential mechanisms through a meta-analysis of field observations. The results showed that warming (+2.0 °C on average) significantly enhanced soil carbon dioxide (CO2) emissions (i.e., soil respiration) by 14.7% and nitrous oxide (N2O) fluxes by 12.6% across croplands and increased soil methane (CH4) uptake by 21.8% in uplands and CH4 release by 23.4% in paddy fields. The responses of C gas fluxes to warming were regulated by initial C substrates, initial wetness, and changes in temperature in croplands. The responses of N2O fluxes to warming were mainly associated with changed NH4+-N and NO3--N as well as initial wetness and N fertilizer in croplands. The responses of soil GHG fluxes to warming were generally comparable among different crop species and N fertilizer levels, respectively. However, the responses of CO2 emissions and CH4 release to warming were significantly higher in upland-paddy fields than in uplands and paddy fields; the warming-induced changes in CH4 release was significantly greater in rotation cropping systems than in single- and double-cropping systems. This synthesis highlights the important role of climate warming in increasing soil GHG fluxes from croplands, underscoring the critical need for agricultural practice adjustment to mitigate climate change in the future.