71 research outputs found

    Ca<sup>2+</sup> Overload Decreased Cellular Viability in Magnetic Hyperthermia without a Macroscopic Temperature Rise

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    Magnetic hyperthermia is a crucial medical engineering technique for treating diseases, which usually uses alternating magnetic fields (AMF) to interplay with magnetic substances to generate heat. Recently, it has been found that in some cases, there is no detectable temperature increment after applying an AMF, which caused corresponding effects surprisingly. The mechanisms involved in this phenomenon are not yet fully understood. In this study, we aimed to explore the role of Ca2+ overload in the magnetic hyperthermia effect without a perceptible temperature rise. A cellular system expressing the fusion proteins TRPV1 and ferritin was prepared. The application of an AMF (518 kHz, 16 kA/m) could induce the fusion protein to release a large amount of iron ions, which then participates in the production of massive reactive oxygen radicals (ROS). Both ROS and its induced lipid oxidation enticed the opening of ion channels, causing intracellular Ca2+ overload, which further led to decreased cellular viability. Taken together, Ca2+ overload triggered by elevated ROS and the induced oxidation of lipids contributes to the magnetic hyperthermia effect without a perceptible temperature rise. These findings would be beneficial for expanding the application of temperature-free magnetic hyperthermia, such as in cellular and neural regulation, design of new cancer treatment methods

    DataSheet1_Pan-Cancer Analysis Identified C1ORF112 as a Potential Biomarker for Multiple Tumor Types.ZIP

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    C1ORF112 is an evolutionarily conserved gene across vertebrates. Over the last decade, studies have suggested that C1ORF112 may play a role in tumorigenesis. Using The Cancer Genome Atlas datasets, we explored the role of C1ORF112 across various tumor types in this study. In most tumor types, C1ORF112 expression was increased in tumor tissues compared to corresponding non-tumor tissues. In patients with certain tumor types, higher C1ORF112 expression was correlated with shorter overall survival, disease-free survival, and progression-free survival. Further analyses of C1ORF112 genetic alteration data showed that C1ORF112 amplification and mutations may have an impact on liver hepatocellular carcinoma and uterine corpus endometrial carcinoma prognosis. In cancers including lower grade glioma and adrenocortical carcinoma, C1ORF112 expression was linked to cancer-associated fibroblast infiltration. Gene Ontology analysis showed that C1ORF112 was co-expressed with genes involved in biological processes such as cell cycle and mitotic regulation. The protein interaction network demonstrated that C1ORF112 physically interacted with RAD51, DMC1, and FIGNL1, which have well characterized functions in DNA repair and cell cycle regulation. This pan-cancer study revealed the prognostic value and oncogenic role of C1ORF112 across multiple tumor types.</p

    Hollow Titania Spheres with Movable Silica Spheres Inside

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    We demonstrate a flexible method for preparing hollow TiO2 nanospheres with movable silica nanoparticles inside (HTNMSNs). In this method, we used monodisperse silica−polystyrene core−shell nanospheres (SiO2-PS-CSNs) sulfonated as templates and prepared the composite shell consisting of TiO2 and sulfonated polystyrene (SPS) through adsorbing or depositing tetrabutyl titanate gel into the SPS shell. Finally the HTNMSNs were obtained after removal of all polymers in the composite nanospheres by dissolution or calcinations. We investigated the dependence of the morphologies of HTNMSNs on the thickness of PS shells and the size of SiO2 cores and prepared rare earth doped HTNMSNs by a sol−gel process

    Reactive Oxygen Species Activate a Ferritin-Linked TRPV4 Channel under a Static Magnetic Field

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    Magnetogenetics has shown great potential for cell function and neuromodulation using heat or force effects under different magnetic fields; however, there is still a contradiction between experimental effects and underlying mechanisms by theoretical computation. In this study, we aimed to investigate the role of reactive oxygen species (ROS) in mechanical force-dependent regulation from a physicochemical perspective. The transient receptor potential vanilloid 4 (TRPV4) cation channels fused to ferritin (T4F) were overexpressed in HEK293T cells and exposed to static magnetic fields (sMF, 1.4–5.0 mT; gradient: 1.62 mT/cm). An elevation of ROS levels was found under sMF in T4F-overexpressing cells, which could lead to lipid oxidation. Compared with the overexpression of TRPV4, ferritin in T4F promoted the generation of ROS under the stimulation of sMF, probably related to the release of iron ions from ferritin. Then, the resulting ROS regulated the opening of the TRPV4 channel, which was attenuated by the direct addition of ROS inhibitors or an iron ion chelator, highlighting a close relationship among iron release, ROS production, and TRPV4 channel activation. Taken together, these findings indicate that the produced ROS under sMF act on the TRPV4 channel, regulating the influx of calcium ions. The study would provide a scientific basis for the application of magnetic regulation in cellular or neural regulation and disease treatment and contribute to the development of the more sensitive regulatory technology

    Table1_Techno-economic assessment of electrolytic hydrogen in China considering wind-solar-load characteristics.docx

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    Hydrogen production by electrolysis is considered an essential means of consuming renewable energy in the future. However, the current assessment of the potential of renewable energy electrolysis for hydrogen production is relatively simple, and the perspective is not comprehensive. Here, we established a Combined Wind and Solar Electrolytic Hydrogen system, considering the influence of regional wind-solar-load characteristics and transmission costs to evaluate the hydrogen production potential of 31 provincial-level regions in China in 2050. The results show that in 2050, the levelized cost of hydrogen (LCOH) in China’s provincial regions will still be higher than 10 ¥/kg, which is not cost-competitive compared to the current hydrogen production from fossil fuels. It is more cost-effective to deploy wind turbines than photovoltaic in areas with similar wind and solar resources or rich in wind resources. Wind-solar differences impact LCOH, equipment capacity configuration, and transmission cost composition, while load fluctuation significantly impacts LCOH and electricity storage configuration. In addition, the sensitivity analysis of 11 technical and economic parameters showed differences in the response performance of LCOH changes to different parameters, and the electrolyzer conversion efficiency had the most severe impact. The analysis of subsidy policy shows that for most regions (except Chongqing and Xizang), subsidizing the unit investment cost of wind turbines can minimize LCOH. Nevertheless, from the perspective of comprehensive subsidy effect, subsidy cost, and hydrogen energy development, it is more cost-effective to take subsidies for electrolysis equipment with the popularization of hydrogen.</p

    Data_Sheet_1_Efficient Genome Editing of Magnetospirillum magneticum AMB-1 by CRISPR-Cas9 System for Analyzing Magnetotactic Behavior.PDF

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    Magnetotactic bacteria (MTB) are a diverse group of microorganisms capable of using geomagnetic fields for navigation. This magnetotactic behavior can help microorganisms move toward favorable habitats for optimal growth and reproduction. A comprehensive understanding of the magnetotactic mechanism at molecular levels requires highly efficient genomic editing tools, which remain underdeveloped in MTB. Here, we adapted an engineered CRISPR-Cas9 system for efficient inactivation of genes in a widely used MTB model strain, Magnetospirillum magneticum AMB-1. By combining a nuclease-deficient Cas9 (dCas9) and single-guide RNA (sgRNA), a CRISPR interference system was successfully developed to repress amb0994 expression. Furthermore, we constructed an in-frame deletion mutant of amb0994 by developing a CRISPR-Cas9 system. This mutant produces normal magnetosomes; however, its response to abrupt magnetic field reversals is faster than wild-type strain. This behavioral difference is probably a consequence of altered flagella function, as suggested with our dynamics simulation study by modeling M. magneticum AMB-1 cell as an ellipsoid. These data indicate that, Amb0994 is involved in the cellular response to magnetic torque changes via controlling flagella. In summary, this study, besides contributing to a better understanding of magnetotaxis mechanism, demonstrated the CRISPR-(d)Cas9 system as a useful genetic tool for efficient genome editing in MTB.</p

    Ultrahigh Polarization-Sensitive Raman Scattering and Photon Emission in a Plasmonic Au/Biphenyl-4-thiol/Ag Nanowire Nanocavity

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    Reducing gap distance to the nanometer range exhibits a strong local electric field enhancement, providing a promising platform for exploring light–matter interactions at the nanoscale. Here, we designed and fabricated an anisotropic nanocavity using monolayer biphenyl-4-thiol (BPT) and WSe2 as a barrier and a Ag nanowire and Au film as a cavity, allowing local electric field enhancement by controlling the polarity of incident light. Strong and polarization-dependent Raman scattering of BPT molecules is observed, which may be applied for mid-infrared light detection. Moreover, the BPT monolayer can act as a uniformly distributed nanometer-size barrier layer to prohibit carrier transferring from WSe2 to the Au film. The nanometer barrier thickness induced a strong localized electric field that altered the carrier recombination paths in monolayer WSe2. Trion emission intensity is enhanced over 520 times at room temperature, and the dark state is observed at a temperature below 253 K. Below 173 K, a new low energy emission peak quickly outweighs the trion, exciton, and dark state emission and dominate the emission spectrum, which could be related to a strong exciton–plasmon coupling. Therefore, the designed nanocavity is an excellent platform to study the abundant emission phenomenon in transition-metal dichalcogenide and related heterostructures

    Image1_Association Study Between Polymorphic Loci in Cholesterol Metabolism Pathway and Gallstone in the Tibetan Population.pdf

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    Background: The incidence of gallstones in the Tibetan population is increasing rapidly. Previous studies indicated that genetic variation located in the cholesterol metabolism pathway may be associated with the incidence of gallstones.Methods: By recruiting 132 Tibetan gallstone patients and 52 normal Tibetan controls, we performed next-generation sequencing for 508 genes in the cholesterol metabolism pathway. Additionally, by integrating the sequence data of 41 normal Tibetan subjects in the public database, we finally obtained 93 normal Tibetan controls. Single nucleotide polymorphisms (SNPs) calling were performed by using the GATK pipeline. The quality control criteria for SNPs were: missing rate 0.01; and p value >0.001 in the Hardy-Weinberg Equilibrium (HWE) test. To eliminate the influence of population heterogeneity, Principal Component Analysis (PCA) was carried out by using the smartpca software. Association analyses were performed by Plink software. Multiple tests were adjusted by the false discovery rate (FDR) method.Results: A total of 2,401 SNPs were obtained by analyzing 508 genes, and 2,011 SNPs left after quality control. After adjusting the eigen vectors, we found that 10 SNPs (SNV05997, rs80145081, rs80005560, rs79074685, rs748546375, rs201880593, rs142559357, rs750769471, rs869789 and rs4072341) were significantly associated with gallstone. Subsequently, by comparing the case group with our control group and the public database control group separately, we further found that the SNP rs869789 was consistently significantly associated with gallstone (p = 9.04 × 10–3 in cases vs. our controls and 5.73 × 10–3 in cases vs. public controls, respectively).Conclusion: By systematically analyzed SNPs in the cholesterol metabolism pathway, we identified one polymorphic locus rs869789 significantly associated with the pathogenesis of gallstone in the Tibetan population. This study will provide clue for further mechanism study of gallstone in the Tibetan population.</p
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