ABSTRACT
Janus heterostructures consisting of multiple jointed components with distinct properties have gained growing interest in the photoredox catalytic field. Herein, we have developed a facile low-temperature method to gain anisotropic one-dimensional Au-tipped CdS (Au-CdS) nanorods (NRs), followed by assembling Ru molecular co-catalyst (RuN5) onto the surface of the NRs. The CdS NRs decorated with plasmonic Au nanoparticles (NPs) and RuN5 complex harness the virtues of metal-semiconductor and inorganic-organic interface, giving directional charge transfer channels, spatially separated reaction sites, and enhanced local electric field distribution. As a result, the Au-CdS-RuN5 can act as an efficient dual-function photocatalyst for simultaneous H2 evolution and valorization of biomass-derived alcohols. Benefiting from the interfacial charge decoupling and selective chemical bond activation, the optimal all-in-one Au-CdS-RuN5 heterostructure shows greatly enhanced photoactivity and selectivity as compared to bare CdS NRs, along with a remarkable apparent quantum yield of 40.2 % at 400â nm. The structural evolution and working mechanism of the heterostructures are systematically analyzed based on experimental and computational results.
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BACKGROUND: Despite the fact that red blood cell (RBC) transfusion is commonly applied in surgical intensive care unit (ICU), the effect of RBC transfusion on long-term outcomes remains undetermined. We aimed to explore the association between RBC transfusion and the long-term prognosis of surgical sepsis survivors. METHODS: This retrospective study was conducted on adult sepsis patients admitted to a tertiary surgical ICU center in China. Patients were divided into transfusion and non-transfusion groups based on the presence of RBC transfusion. Propensity score matching (PSM) and inverse probability of treatment weighting (IPTW)were performed to balance the potential confounders. RESULTS: A total of 1421 surgical sepsis survivors were enrolled, including 403 transfused patients and 1018 non-transfused patients. There was a significant difference in 1-year mortality between the two groups (23.1 â% vs 12.7 â%, HR: 1.539, 95 â% confidence interval [CI]: 1.030-2.299, P â< â0.001). After PSM and IPTW, transfused patients still showed significantly increased 1-year mortality risks compared to non-transfused individuals (PSM: 23.6 â% vs 15.9 â%, HR 1.606, 95 â% CI 1.036-2.488 âP â= â0.034; IPTW: 20.1 â% vs 12.9 â%, HR 1.600, 95 â% CI 1.040-2.462 âP â= â0.032). Among patients with nadir hemoglobin below 70 âg/L, 1-year mortality risks in both groups were similar (HR 1.461, 95 â% CI 0.909-2.348, P â= â0.118). However, among patients with nadir hemoglobin above 70 âg/L, RBC transfusion was correlated with increased 1-year mortality risk (HR 1.556, 95 â% CI 1.020-2.374, P â= â0.040). CONCLUSION: For surgical sepsis survivors, RBC transfusion during ICU stay was associated with increased 1-year mortality, especially when patients show hemoglobin levels above 70 âg/L.
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Efficient utilization of sunlight in photocatalysis is widely recognized as a promising solution for addressing the growing energy demand and environmental issues resulting from fossil fuel consumption. Recently, there have been significant developments in various near-infrared (NIR) light-harvesting systems for artificial photosynthesis and photocatalytic environmental remediation. This review provides an overview of the most recent advancements in the utilization of NIR light through the creation of novel nanostructured materials and molecular photosensitizers, as well as modulating strategies to enhance the photocatalytic processes. A special focus is given to the emerging two-photon excitation NIR photocatalysis. The unique features and limitations of different systems are critically evaluated. In particular, it highlights the advantages of utilizing NIR light and two-photon excitation compared to UV-visible irradiation and one-photon excitation. Ongoing challenges and potential solutions for the future exploration of NIR light-responsive materials are also discussed.
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Regeneration enables the regrowth and restoration of missing body parts. It is a common phenomenon among animals. However, only some species exhibit remarkable regeneration capabilities and can regenerate organs such as limbs, lenses or hearts. Regeneration has been widely studied, thereby giving rise to new fields, such as regenerative medicine. Furthermore, regeneration has the potential to be applied to the human body. However, the molecular mechanisms governing this process should be elucidated first. Recent advancements in research methods have led to the identification of numerous signaling pathways involved in regeneration. One of them, the Wnt transduction pathway, is an ancient and evolutionarily conserved pathway that plays an important role in both embryonic development and regeneration. The Wnt pathway plays an important role during the regeneration process, as it is implicated in cell fate determination, cell migration, cell polarity and adult cell homeostasis. To date, two major Wnt pathways have been identified: the canonical (ß-catenin dependent) pathway and the non-canonical pathway. The latter pathway can be further divided into planar cell polarity, the Wnt/Ca2+ pathway and the JNK pathway. In this review, we summarize the current state of knowledge regarding the Wnt signaling pathway and its role in regeneration, with a particular emphasis on key model species.
Subject(s)
Heart , Wnt Signaling Pathway , Animals , beta Catenin/metabolism , Cell Differentiation/physiology , Embryonic Development , Models, Animal , Wnt Signaling Pathway/physiologyABSTRACT
Heterojunctions have been proved to be the promising photocatalysts for hazardous contaminants removal, but the inferior interfacial contact, low carrier mobility and random carrier diffusion seriously hamper the photoactivity improvement of the conventional heterojunctions. Herein, SO chemically bonded p-n oriented heterostructure is fabricated via selectively anchoring of p-type Ag2S nanoparticles on the lateral facet of n-type Bi4TaO8Cl nanosheet. Such a p-n heterojunction engineering on specific facet of Bi4TaO8Cl semiconductor derives ingenious double internal electric field (IEF), which not only effectively creates the spatially separated oxidation and reduction sites, but also delivers the powerful driving forces for impactful spatial directed photocarrier transfer along the cascade path. Additionally, our experimental and theoretical analyses jointly signify that the interfacial SO bond could serve as an efficient atomic-level interfacial channel, which is conducive to encouraging the vectorial charge separation and migration kinetic. As a result, the Ag2S/Bi4TaO8Cl oriented heterojunction exhibits significantly enhanced visible light driven photocatalytic redox ability for tetracycline oxidation and hexavalent chromium reduction than those of single component and the traditional random/mixed heterojunctions. This study could provide a deeper insight into the synergistic effects of multi-IEF modulation and interfacial chemical bond bridging on optimizing the photogenerated carrier behaviors.
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A small specific surface area and severe charge carrier recombination greatly limit the photocatalytic efficiency of semiconductors. Herein, we developed a novel wet-chemical intercalation strategy by using the NaBH4 reagent for in situ intercalation-assisted expansion and surface/interface reconstruction of Bi4TaO8Br, which exhibits an enhanced specific surface area and charge carrier separation features. This work highlights intercalation of semiconductors for achieving enhanced photocatalytic performance and provides a new idea to synergistically regulate the morphology and surface/interface composition of semiconductors.
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OBJECTIVE: Ultraviolet-B (UVB) radiation is an important factor in causing skin damage. The study is to explore whether 1,25-Dihydroxvitamin D3(1,25(OH)2D3) will attenuate the damage of human immortalised keratinocytes (HaCaT) cells caused by UVB and relevant underlying mechanisms. METHODS: CCK-8 was employed to determine the UVB irradiation intensity and 1,25(OH)2D3 concentration. Western blot was used to detect the expression of NF-κB, Caspase9, Caspase3, Bax, Bcl2, FADD, CytC, Beclin-1; Flowcytometry was applied to measure the production of ROS. RESULTS: The concentration of 1,25(OH)2D3 used in the study was 100 nM and the UVB irradiation intensity was 20 mJ/cm2. Compared with the HaCaT cells irradiated with UVB, the HaCaT cells that were pre-treated with 1,25(OH)2D3 had lower production of ROS, lower expression of NF-κB, Caspase9, Caspase3, Bax, FADD, CytC and Beclin-1(P < 0.05). CONCLUSION: 1,25(OH)2D3 could inhibit the development of oxidative stress and apoptosis in HaCaTs triggered by UVB. This inhibition might be achieved through the suppression of mitochondria-modulated apoptosis and autophagy. Vitamin D may be a potential UVB protective component.
Subject(s)
Keratinocytes , NF-kappa B , Humans , Reactive Oxygen Species/metabolism , NF-kappa B/metabolism , Beclin-1/metabolism , bcl-2-Associated X Protein/metabolism , Keratinocytes/metabolism , Apoptosis/radiation effects , Ultraviolet Rays/adverse effectsABSTRACT
Perfluorooctanoic acid is an artificial and non-degradable chemical. It is widely used due to its stable nature. It can enter the human body through food, drinking water, inhalation of household dust and contact with products containing perfluorooctanoic acid. It accumulates in the human body, causing potential harmful effects on human health. Based on the biodegradability and bioaccumulation of perfluorooctanoic acid in the human body, there are increasing concerns about the adverse effects of perfluorooctanoic acid exposure on kidneys. Research shows that kidney is the main accumulation organ of Perfluorooctanoic acid, and Perfluorooctanoic acid can cause nephrotoxicity and produce adverse effects on kidney function, but the exact mechanism is still unknown. In this review, we summarize the relationship between Perfluorooctanoic acid exposure and kidney health, evaluate risks more clearly, and provide a theoretical basis for subsequent research.
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BACKGROUND: Nile tilapia (Oreochromis niloticus), an important economic freshwater fish being cultured globally, is highly adaptable to a wide range of salinities. However, little information is currently available on the mechanism of salinity adaptation. OBJECTIVE: For a better understanding of this intriguing adaptability, we identified and analyzed aquaporins (AQPs), which are channel proteins with a basic function of intracellular and intercellular transportation for water and certain solutes. METHODS: In the present study, we performed genome-wide identification and comprehensive analysis of the duplicated AQP genes in Nile tilapia by bioinformatics methods. Tissue-specific analyses were then combined with transcriptome data under different salinity treatments. RESULTS: It was revealed that Nile tilapia has a total of twenty-eight AQPs, which are distributed unevenly on twelve chromosomes and belong to four subfamilies according to phylogenetic analysis. These AQPs share conserved AQP characteristic structural domains and motifs, although they differ in molecular weight from 23 to 36 kDa and contain distinct sequences. GO analysis revealed that most AQPs have transporter protein activity and are involved in biological processes such as substance transport, stress response, development and metabolism. KEGG enrichment analysis showed that AQPs were significantly enriched in two pathways, anti-diuretic hormone-regulated reabsorption and bile secretion. CONCLUSION: These results suggested that Nile tilapia has a highly developed, albeit complex, osmotic pressure regulation system, which provided a molecular basis for exploring how these AQP members coordinate to help Nile tilapia cope with different salinities.
Subject(s)
Aquaporins , Cichlids , Animals , Cichlids/genetics , Cichlids/metabolism , Salinity , Phylogeny , Aquaporins/genetics , Aquaporins/metabolism , TranscriptomeABSTRACT
(1) Background: Perfluorooctane sulfonate (PFOS) is a persistent organic pollutant, and it is receiving increasing attention regarding its human health risks due to its extensive use. Endothelial dysfunction is a mark of cardiovascular disease, but the basic mechanism of PFOS-induced endothelial dysfunction is still not fully understood. Ferroptosis is a newly defined regulatory cell death driven by cellular metabolism and iron-dependent lipid peroxidation. Although ferroptosis has been shown to be involved in the pathogenesis of cardiovascular diseases, the involvement of ferroptosis in the pathogenesis of endothelial dysfunction caused by PFOS remains unclear. (2) Purpose: To explore the role of ferroptosis in the dysfunction of endothelial cells and underlying mechanisms. (3) Methods: Human umbilical vein endothelial cells (HUVECs) were exposed to PFOS or PFOS and Fer-1. The viability, morphology change under electronic microscope, lipid-reactive oxygen species (lipid-ROS), and production of nitric oxide (NO) were determined. The expression of glutathione peroxidase 4(GPX4), ferritin heavy chain protein 1 (FTH1), heme oxygenase 1 (HO-1) and Acyl-CoA synthetase long-chain family member 4 (ACSL4) were analyzed via Western blot analysis. (4) Results: PFOS was shown to cause a decrease in viability and morphological changes of mitochondria, and well as an increase in lipid droplets. The expression of GPX4, FTH1 and HO-1 was decreased, and that of ACSL4 was increased after exposure to PFOS. In addition to the above-mentioned ferroptosis-related manifestations, there was also a reduction in NO content. (5) Conclusions: PFOS induces ferroptosis by regulating the GPX4 and ACSL4 pathways, which leads to HUVEC dysfunction.
ABSTRACT
Perfluorooctane sulfonate (PFOS) is a typical persistent organic pollutant and environmental endocrine disruptor that has been shown to be associated with the development of many diseases; it poses a considerable threat to the ecological environment and to human health. PFOS is known to cause damage to renal cells; however, studies of PFOS-induced ferroptosis in cells have not been reported. We used the CCK-8 method to detect cell viability, flow cytometry and immunofluorescence methods to detect ROS levels and Western blot to detect ferroptosis, endoplasmic reticulum stress, antioxidant and apoptosis-related proteins. In our study, we found that PFOS could induce the onset of ferroptosis in HK-2 cells with decreased GPx4 expression and elevated ACSL4 and FTH1 expression, which are hallmarks for the development of ferroptosis. In addition, PFOS-induced ferroptosis in HK-2 cells could be reversed by Fer-1. We also found that endoplasmic reticulum stress and its mediated apoptotic mechanism and P53-mediated antioxidant mechanism are involved in the toxic damage of cells by PFOS. In this paper, we demonstrated for the first time that PFOS can induce ferroptosis in HK-2 cells. In addition, we preliminarily explored other mechanisms of cytotoxic damage by PFOS, which provides a new idea to study the toxicity of PFOS as well as the damage to the kidney and its mechanism.
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H2V3O8/GaN n-n heterojunction ultraviolet photodetectors are fabricated via a facile dip-coating method. The Schottky junction between the GaN and H2V3O8 builds a built-in electric field to achieve the self-powered phenomenon. The photodetector presents a high photocurrent (0.23 µA) and a fast response speed (less than 0.3 s) at 0 V bias and under 365 nm light illumination (24.50 mW cm-2). Furthermore, the photocurrent increases steadily as the light intensity increases from 0.53 to 24.50 mW cm-2. The H2V3O8/GaN heterojunction holds great potential to realize high-performance hybrid PDs.
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Perfluorooctane sulfonate (PFOS) is a persistent, widely present organic pollutant. PFOS can enter the human body through drinking water, ingestion of food, contact with utensils containing PFOS, and occupational exposure to PFOS, and can have adverse effects on human health. Increasing research shows that the liver is the major target of PFOS, and that PFOS can damage liver tissue and disrupt its function; however, the exact mechanisms remain unclear. In this study, we reviewed the adverse effects of PFOS on liver tissue and cells, as well as on liver function, to provide a reference for subsequent studies related to the toxicity of PFOS and liver injury caused by PFOS.
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The traditional heterogeneous photo-Fenton reaction was mainly restricted by the fewer surface-active sites, low Fe3+/Fe2+ transformation and H2O2 activation efficiency of catalyst. This work designed and fabricated the efficient photo-Fenton Schottky catalysts via a facile electrostatic self-assembly of metallic Fe2N nanoparticles scattering on the surface of red g-C3N4 (ultrathin porous oxygen-doped 2D g-C3N4 nanosheets). The porous morphology and exceptional electrical structure of red g-C3N4 endowed more active sites and facilitated the photoexcited charge separation. Benefitting from the Schottky effect and unique dimensional coupling structure, the strong visible light absorption and fast spatial charge transfer were realized in the Schottky junction system. More strikingly, Fe2N as an efficient co-catalyst was in favor of the trap and export of e-, leading to the Fe3+/Fe2+ transformation and H2O2 activation during the photo-Fenton process. Accordingly, the as-prepared catalysts revealed outstanding activity in photo-Fenton like degradation of tetracycline (TC) although under 5 W white LED light irradiation. Furthermore, the reasonable degradation pathway of TC and corresponding toxicity of the intermediates, as well as the photo-Fenton catalytic mechanism were interpreted and discussed in detail. This study would be a great aid in the development of various Schottky catalysts for heterogeneous photo-Fenton-based environmental remediation systems.
Subject(s)
Hydrogen Peroxide , Tetracycline , Catalysis , Porosity , Static ElectricityABSTRACT
This study demonstrates the rational design and construction of a BiOBr/Bi4MoO9 edge-on heterostructure by growing fish scale-like BiOBr nanosheets on the surface of Bi4MoO9. Such structural and compositional merits expedite electron transport and offer a large interfacial contact area and abundant reactive sites. Optimized BiOBr/Bi4MoO9 exhibited outstanding TC degradation activity.
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Investigations into novel single-phase phosphors with outstanding luminescence properties and excellent thermal stability are urgently needed in the lighting field. In this work, a crystal phase transition and polyhedron transformation strategy via cation substitution has been proposed. Via controlling the Sr/Ba ratio, the structural evolution of the phosphor from a monocelsian phase to a hexacelsian or feldspar phase and the variation of the local environments of Eu2+ sites are correspondingly studied in Ba0.47-xSr0.50+xAl2Si2O8:0.03Eu. Consequently, the optimal Ba0.17Sr0.80Al2Si2O8:0.03Eu sample exhibits a higher intensity, up to 15.2-fold that of Ba0.97Al2Si2O8:0.03Eu. A narrower full-width-at-half-maximum of 73 nm, better color purity of 82.96%, and an internal quantum yield of 82.3% can be realized. With an increase in temperature, the emission intensity losses of samples from x = -10.0-47.0% are no more than 10.0% at 473 K. Moreover, a WLED (CCT = 5210 K; CRI = 90.3) fabricated using Ba0.17Sr0.80Al2Si2O8:0.03Eu displays warmer white light than one fabricated using BaMgAl10O17:Eu under the same assembly and test conditions. Analysis shows that the structural evolution with reduced polyhedral symmetry and the condensed crystal structure with fortified rigidity are responsible for the improvement in properties. This discovery demonstrates that the utilization of a crystal phase transition and symmetrical coordination is an efficient way to develop novel efficient phosphors and other related materials.
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Evolutionary developmental biology, or Evo-Devo for short, has become an established field that, broadly speaking, seeks to understand how changes in development drive major transitions and innovation in organismal evolution. It does so via integrating the principles and methods of many subdisciplines of biology. Although we have gained unprecedented knowledge from the studies on model organisms in the past decades, many fundamental and crucially essential processes remain a mystery. Considering the tremendous biodiversity of our planet, the current model organisms seem insufficient for us to understand the evolutionary and physiological processes of life and its adaptation to exterior environments. The currently increasing genomic data and the recently available gene-editing tools make it possible to extend our studies to non-model organisms. In this review, we review the recent work on the regulatory signaling of developmental and regeneration processes, environmental adaptation, and evolutionary mechanisms using both the existing model animals such as zebrafish and Drosophila, and the emerging nonstandard model organisms including amphioxus, ascidian, ciliates, single-celled phytoplankton, and marine nematode. In addition, the challenging questions and new directions in these systems are outlined as well.
Subject(s)
Biodiversity , Biological Evolution , Developmental Biology , Models, Animal , Animals , GenomicsABSTRACT
Among vertebrates, urodele amphibians possess a unique ability to regenerate various body parts including limbs. However, reports of their digit regeneration remain scarce, especially information about the related genes. In this study, it was evident that matrix metalloproteinases (mmps) including mmp9, mmp3/10a, and mmp3/10b, which play a crucial role in tissue remodeling, are highly expressed during early stages of digit regeneration in axolotl. Using in situ hybridization, we revealed that wound epidermis and blastema are two major origins of the MMPs during the regeneration process. Additionally, we found that the inhibition of MMPs with GM6001 (a wide-spectrum inhibitor of MMPs) in vivo after amputation disturbed normal digit regeneration process and resulted in malformed regenerates. Furthermore, inhibition of MMPs hindered blastema formation and decreased cell apoptosis at early stages in the digit regenerates. All these points suggest that MMPs are required for digit regeneration, as they play a significant role in the regulation of blastema formation.
Subject(s)
Extremities/physiopathology , Matrix Metalloproteinases/metabolism , Regeneration/genetics , Ambystoma mexicanum , Animals , Disease Models, AnimalABSTRACT
As increasing demand for noncontact temperature sensing, the development of a high-performance optical thermometer probe is more and more urgent. In this work, an efficient dual-mode optical thermometry strategy based on the Pr3+/Dy3+ energy transfer (ET) in some typical double-perovskite oxides is presented, which offers a promising way to design FIR/lifetime dual-mode optical thermometry with excellent temperature-measuring sensitivity and signal discrimination. According to this strategy, double-perovskite La2MgTiO6:Pr3+/Dy3+ phosphors are successfully synthesized. On the basis of diverse thermal responses between Pr3+ and Dy3+, the FIR of Pr3+ to Dy3+ (four FIR mode) in this material displays outstanding optical thermometry performance from 298 to 548 K. The maximum absolute and relative sensitivities (Sa and Sr) of mode 1 are 0.09 and 2.357% K-1, being better than the current optical temperature measurement materials. For the fluorescence lifetime mode, the Sa-max and Sr-max values reach 2.85 × s 10-4 and 1.814% K-1. Furthermore, the dual-mode optical thermometry mechanism was presented and studied. It also demonstrated excellent optical thermometry performance in the other Pr3+/Dy3+ codoped double-perovskite oxides, such as LaMg0.598Nb0.402O3, NaLa(MoO4)2, NaGd(MoO4)2, and NaLa(WO4)2, proving the universality of the presented strategy. This article presents an effective Pr3+/Dy3+ ET pathway for developing new and highly sensitive FIR/lifetime dual-mode optical temperature sensing materials.