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Background Abnormal metabolism, including abnormal lipid metabolism, is a hallmark of cancer cells. Some studies have demonstrated that the lipogenic pathway might promote the development of hepatocellular carcinoma (HCC). However, the role of the lipolytic pathway in HCC has not been elucidated. Methods We compared levels of adipose triglyceride lipase (ATGL) in human HCC and healthy liver tissues by real time PCR, western blot and immunohistochemistry. We measured diacylglycerol(DAG) and free fatty acid (FFA) levels in HCC cells driven by the NEAT1 -ATGL axis and in HCC tissues. We also assessed the effects of ATGL, DAG, FFA, and NEAT1 on HCC cells proliferation in vitro and in an orthotopic xenograft HCC mouse model. We also performed a luciferase reporter assay to investigate the interaction between NEAT1 /ATGL and miR-124-3p. Results We found that the lipolytic enzyme, ATGL is highly expressed in human HCC tissues and predicts poor prognosis. We also found that high levels of DAG and FFA are present in HCC tissues. Furthermore, the lncRNA- NEAT1 was found to modulate ATGL expression and disrupt lipolysis in HCC cells via ATGL . Notably, ATGL and its products, DAG and FFA, were shown to be responsible for NEAT1 -mediated HCC cell growth. NEAT1 regulated ATGL expression by binding miR-124-3p. Additionally, NEAT1 knockdown attenuated HCC cell growth through miR-124-3p/ATGL/DAG+FFA/PPARα signaling. Conclusion Our results reveal that NEAT1- modulates abnormal lipolysis via ATGL to drive HCC proliferation.

Radiofrequencies have shown efficacy in addressing skin aging. Despite their effectiveness, few studies have explored how radiofrequencies affect the skin transcriptome. This study utilized mouse models divided into two age groups (four-month-old and one-year-old mice) to assess the impact of a radiofrequency device on skin collagen and elastin. A combination of histological analysis, Western blot analysis, real-time PCR and transcriptome sequencing was employed. Histological analysis revealed significant increases in dermis thickness and collagen fiber volume following radiofrequency treatment in both age groups. Quantitative PCR and Western blot analysis indicated that the levels of collagen-related genes and proteins were higher in the four-month-old group. Transcriptome sequencing identified 465 and 1867 differentially expressed genes (DEGs) in the skin of the 4-month-old mice and 1-year-old mice, respectively. GO and KEGG analyses elucidated the molecular mechanisms, revealing that the interleukin-17 and tumor necrosis factor signaling pathways may play crucial roles in collagen regeneration induced by radiofrequencies. Additionally, decreased expression of matrix metalloproteinase-9 and increased expression of the transcription factor Fos were identified as potential biomarkers of collagen regeneration. Immunofluorescence and immunohistochemistry staining demonstrated that radiofrequencies activate fibroblasts and inhibit macrophage alternative activation in the skin. This study identifies key genes and biological pathways involved in radiofrequency treatment and provides a foundation for a deeper understanding of the molecular mechanisms underlying collagen regeneration facilitated by radiofrequencies.

Background Intervertebral disc degeneration (IDD) and vertebral endplate Modic changes (MCs) are common lumbar degenerative phenotypes related to low back pain (LBP). Dyslipidemia has been linked to LBP but its associations with IDD and MCs have not been fully elucidated. The present study aimed to address the possible link between dyslipidemia, IDD and MCs in the Chinese population. Methods 1035 citizens were enrolled in the study. The levels of serum total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C) and triglycerides (TG) were collected. IDD was evaluated based on the Pfirrmann grading system and subjects with an average grade ≥ 3 were defined as having degeneration. MCs were classified into typical types 1, 2 and 3. Covariables, including age, sex, BMI and fasting plasma glucose, were included for the adjustment of the logistic analyses. Results The degeneration group included 446 subjects while the nondegeneration group included 589 subjects. The degeneration group had significant higher levels of TC and LDL-C ( p  < 0.001) whereas TG and HDL-C were not significantly different between the two groups. TC and LDL-C concentrations were significantly positively correlated with average IDD grades ( p  < 0.001). Multivariate logistic regression revealed that high TC (≥ 6.2 mmol/L, adjusted OR = 1.775, 95% CI = 1.209–2.606) and high LDL-C (≥ 4.1 mmol/L, adjusted OR = 1.818, 95% CI = 1.123–2.943) were independent risk factors for IDD. Type 1 MC presented in 84 (8.12%) subjects, type 2 MC presented in 244 (23.57%) subjects, type 3 MC presented in 27 (2.61%) subjects and no MC was observed in the remaining 680 (65.70%) subjects. The type 2 MC group demonstrated a higher level of TC, but the association between serum lipids and MCs could not be confirmed in further multivariate logistic regression. Conclusions High TC (≥ 6.2 mmol/L) and LDL-C (≥ 4.1 mmol/L) concentrations were independent risk factors for IDD for citizens in China. However, the association between dyslipidemia and MCs could not be determined. The effect of excess serum cholesterol may be critical for IDD and cholesterol lowering treatment may provide new opportunities in the management of lumbar disc degeneration.

In regions characterised by high humidity and abundant vegetation, the external insulation materials utilised in high‐voltage transmission and transformation are frequently fouled with a multitude of microorganisms, thereby jeopardising the reliable operation of the power grid. A comprehensive overview of the periodic growth regulation of parasitic algae is presented upon insulating composites across various regions of the world. Additionally, it highlights the methods for quantitative evaluation and accurate prediction of algae coverage degree. Also, the biological contaminates coating process and the artificial flashover test method are summarised, and the effects of algae on the reliability of inorganic and organic materials used for external insulation are compared. It emphasises the dynamic hygroscopic characteristics and cytoelectronegativity of cell secretions as the critical factors that negatively affect the hydrophobicity and flashover performance of silicone rubber insulators by algae. Furthermore, valuable insights into the long‐term inhibition of algae growth on polymeric insulators are provided using eco‐friendly antibiotic‐loaded silica aerogel nanocomposites. A comprehensive overview of the periodic growth regulation of parasitic algae upon insulating composites is presented across various regions of the world. Additionally, it highlights the methods for quantitative evaluation and accurate prediction of algae coverage degree. Also, the biological contaminates coating process and the artificial flashover test method are summarised, and the effects of algae on the reliability of inorganic and organic materials used for external insulation are compared. Furthermore, valuable insights into the long‐term inhibition of algae growth on polymeric insulators are provided using eco‐friendly antibiotic‐loaded silica aerogel nanocomposites.

Tensile experiments were conducted for Al-7.0Zn-2.5Mg-2.0Cu-0.1Zr-0.2Sc alloy in different aging states (18 h, 24 h, 36 h) with temperature environments including room temperature, −10 °C and −30 °C. Comparative studies were made on the evolution of the precipitate phase in alloys at three kinds of aging times and the evolution of tensile properties in alloys under different ambient temperatures. The findings showed that the precipitates in Al-7.0Zn-2.5Mg-2.0Cu-0.1Zr-0.2Sc alloy were mainly in the GP zone after the solution + aging treatment η’ phase, the secondary Al3 (Sc, Zr) phase and the θ’ (Al2Cu) phase. As the aging time was prolonged, the η’ phase gradually grew and the PFZ gradually widened. At the three test temperatures, the tensile strength (TS) and yield strength (YS) of the alloys both showed a trend of first increasing before decreasing with the extension of aging time, while the elongation (A) and section shrinkage (Z) showed a decreasing trend. As the test temperature decreased, the TS and YS of the alloys increased and the A and Z of the alloys decreased. At room temperature, alloys showed a ductile fracture mode, which changed to mixed ductile and brittle fracture with decreasing test temperature.

Gastrointestinal (GI) diseases pose a major clinical burden, yet conventional histopathology suffers from subjectivity and limited reproducibility. While existing computational pathology foundation models are often validated across many subspecialties in “broad but shallow” benchmarks, they rarely demonstrate deep clinical utility in real-world scenarios. To address this, we develop Digepath—a disease-specialized foundation model focused exclusively on high-impact GI pathology. Our approach employs a two-stage iterative optimization: first, pretraining on over 353 million multi-scale patches from 210,043 H&E-stained slides; second, fine-tuning on 471,443 expert-annotated regions, balancing tumor and non-tumor samples to enhance lesion perception amid sparse pathology in whole-slide images. Digepath achieves state-of-the-art performance on 32 of 33 systematic downstream tasks in GI pathology—including diagnosis, molecular profiling, and survival prognosis—demonstrating robust generalization. Moreover, we integrate its capabilities into an agent-based clinical reasoning framework that supports end-to-end intelligent diagnostic workflows, paving the way for real-world deployment.

Carbapenem-resistant Klebsiella pneumoniae (CRKP), one of the major nosocomial pathogens, is increasingly becoming a serious threat to global public health. There is an urgent need to develop effective therapeutic and preventive approaches to combat the pathogen. Here, we identified and characterized a novel capsule depolymerase (K64-ORF41) derived from Klebsiella phage SH-KP152410, which showed specific activities for K. pneumoniae K64-serotype. We showed that this depolymerase could be used in the identification of K64 serotypes based on the capsular typing, and the results agreed well with those from the conventional serotyping method using antisera. From this study, we also identified K64 mutant strains, which showed typing discrepancy between wzi-sequencing based genotyping and depolymerase-based or antiserum-based typing methods. Further investigation indicated that the mutant strain has an insertion sequence (IS) in wcaJ, which led to the alteration of the capsular serotype structure. We further demonstrated that K64-ORF41 depolymerase could sensitize the bacteria to serum or neutrophil killing by degrading the capsular polysaccharide. In summary, the identified K64 depolymerase proves to be an accurate and reliable tool for capsular typing, which will facilitate the preventive intervention such as vaccine development. In addition, the polymerase may represent a potential and promising therapeutic biologics against CRKP-K64 infections.

Background Numerous studies have demonstrated that tetraspanin 1 (TSPAN1), a transmembrane protein, functions as an oncoprotein in many cancer types. However, its role and underlying molecular mechanism in cholangiocarcinoma (CCA) progression remain unclear. Methods In the present study, the expression of TSPAN1 in human CCA and adjacent nontumor tissues was examined using real-time PCR, western blot and immunohistochemistry. The effect of TSPAN1 on proliferation and metastasis was evaluated by functional assays both in vitro and in vivo. A luciferase reporter assay was performed to investigate the interaction between microRNA-194-5p (miR-194-5p) and TSPAN1 3′-untranslated region. Co-immunoprecipitation (co-IP) was used to confirm the interaction between TSPAN1 protein and integrin α6β1 and western blot was used to explore TSPAN1 mechanism. Results We found that TSPAN1 was frequently upregulated in CCA and high levels of TSPAN1 correlated with TNM stage, especially metastasis in CCA. TSPAN1 overexpression promoted CCA growth, metastasis, and induced epithelial-to-mesenchymal transition (EMT), while its silencing had the opposite effect both in vitro and in vivo. To explore the differential expression of TSPAN1, we screened miR-194-5p as the upstream regulator of TSPAN1. A combination of high-level TSPAN1 and low-level miR-194-5p predicted poor prognosis in patients with CCA. Furthermore, in accordance with the functional characteristics of the TSPAN superfamily, we proved that TSPAN1 interacted with integrin α6β1 to amplify the phosphoinositide-3-kinase (PI3K)/AKT/glycogen synthase kinase (GSK)-3β/Snail family transcriptional repressor (Snail)/phosphatase and tensin homolog (PTEN) feedback loop. Conclusion The results indicate that TSPAN1 could be a potential therapeutic target for CCA.

High-voltage bushings play a crucial role in energy conveyance. Their specialized electric structure makes the bushing more vulnerable to surface discharge. However, the influence of a vertical electric field on the surface flashover of bushing structures remains unclear. To investigate this mechanism, four simplified bushing samples were built and the influence of pollution, leakage length, and the electric field component vertical to the dielectric surface on flashover properties of the bushing samples were tested. It was found that the surface pollution level was the decisive factor that influenced flashover voltage. When the leakage length and form factor were the same, the pollution flashover of the bushing structure was lower than that of the post structure. It was also found that increasing the leakage length was not very effective in improving the flashover voltage of bushings when the equivalent salt deposit density (ESDD) was high. No obvious correlation was found between pollution flashover voltage and electric field stress. Furthermore, the uneven wetting flashover performance of the bushings was tested. Under this condition, the flashover voltage decreased with an increase of the electric field component vertical to the dielectric surface. In addition, the electric field distribution of the samples was calculated and the results were in accordance with the experimental results.