Polystyrene nanoparticles strengthen high glucose toxicity associated with alteration in insulin signaling pathway in C. elegans

Using Caenorhabditis elegans as animal model, we investigated the effect of exposure to polystyrene nanoparticles (PS-NPs) in the range of μg/L on high glucose toxicity induction. With lifespan and locomotion behavior as endpoints, we observed that PS-NP (10 and 100 μg/L) enhanced toxicity in 50 mM glucose treated animals. In insulin signaling pathway, expressions of genes encoding insulin receptor (daf-2), kinases (age-1 and akt-1/2), and insulin peptides (ins-9, ins-6, and daf-28) were increased, and expressions of daf-16 and its target of sod-3 were decreased in high glucose treated nematodes followed by PS-NP exposure. Toxicity enhancement in high glucose treated nematodes by PS-NP exposure was inhibited by RNAi of daf-2, age-1, akt-2, akt-1, and 3 insulin peptides genes, but increased by RNAi of daf-16 and sod-3. The resistance of animals with RNAi of daf-2 to toxicity in high glucose treated nematodes followed by PS-NP exposure could be suppressed by RNAi of daf-16. Moreover, in high glucose treated animals followed by PS-NP exposure, daf-2 expression was inhibited by RNAi of ins-6, ins-9, and daf-28. Our data demonstrated the risk of PS-NP exposure in enhancing the high glucose toxicity. More importantly, alteration in expression of genes in insulin signaling pathway was associated with the toxicity enhancement in high glucose treated nematodes followed by PS-NP exposure

Heterogeneous Attributed Network Embedding with Graph Convolutional Networks

Network embedding which assigns nodes in networks to lowdimensional representations has received increasing attention in recent years. However, most existing approaches, especially the spectral-based methods, only consider the attributes in homogeneous networks. They are weak for heterogeneous attributed networks that involve different node types as well as rich node attributes and are common in real-world scenarios. In this paper, we propose HANE, a novel network embedding method based on Graph Convolutional Networks, that leverages both the heterogeneity and the node attributes to generate high-quality embeddings. The experiments on the real-world dataset show the effectiveness of our method

17β-estradiol modulates the viability, phenotype, endocytosis, and inflammatory cytokine expression of RAW264.7 macrophages

17β-estradiol (E2) is a female sex steroid hormone and exerts a pivotal role not only in female pregnancy but also in organ immune responses. Macrophages, as a kind of antigen-presenting cells, play an important influence on the cellular and humoral immune responses and also express the E2 receptor. In the present study, we explored the effects of E2 on the viability, endocytosis, surface molecule, and inflammatory cytokine expression of RAW264.7 macrophages. Results showed that E2 slightly increased the cell proliferation and endocytosis of RAW264.7 cells, while notably decreasing the mRNA and protein levels of inflammatory cytokines such as tumor necrosis factor (TNF)-α and monocyte chemoattractant protein-1 (MCP-1). As for the expression of surface molecules closely associated with the functions of macrophages, E2 significantly reduced the levels of CD40, CD80, and MHC-II. Interestingly, E2 reduced the levels of CD86 at low dose (10 nM and 1 nM), while enhancing its expression at high doses (1 μM and 0.1 μM). These results suggest that E2 may play an immuno-suppressive role in the inflammatory reactions and some autoimmune diseases partly by influencing the expressions of some important surface molecules and inflammatory cytokines of macrophages

Photothermal Catalytic Reduction of CO₂ by Cobalt Silicate Heterojunction Constructed from Clay Minerals

The coupled utilization of solar and thermal energy is considered an efficient way to improve the efficiency of CO2 reduction. Herein, palygorskite (Pal) clay is as a silicon source, while Co2+ is introduced to prepare two-dimensional Co2SiO4 nanosheets, and the excess of Co2+ leads to the growth of Co3O4 on the surface of Co2SiO4 to obtain an S-scheme Co2SiO4/Co3O4−x heterojunction, which facilitates the charge transfer and maintains higher redox potentials. Benefiting from black color and a narrow band gap, the cobalt oxide on the surface can increase the light absorption and produce a local photothermal effect. Under proper thermal activation conditions, the photoelectrons captured by the abundant oxygen vacancies can obtain a secondary leap to the semiconductor conduction band (CB), suppressing the recombination of electron-hole pairs, thus favoring the electron transfer on Co2SiO4/Co3O4−x. The composites not only have abundant oxygen vacancies, but also have a large specific surface area for the adsorption and activation of CO2. The yields of CH3OH on Co2SiO4/Co3O4−5% reach as high as 48.9 μmol·g−1·h−1 under simulated sunlight irradiation. In situ DRIFTS is used to explore the photocatalytic reduction CO2 mechanism. It is found that the thermal effect facilitates the generation of the key intermediate COOH* species. This work provides a new strategy for photothermal catalytic CO2 reduction by taking advantage of natural clay and solar energy

Design, Synthesis, and Biological Evaluation of Novel 6H-Benzo[c]chromen-6-one Derivatives as Potential Phosphodiesterase II Inhibitors

Urolithins (hydroxylated 6H-benzo[c]chromen-6-ones) are the main bioavailable metabolites of ellagic acid (EA), which was shown to be a cognitive enhancer in the treatment of neurodegenerative diseases. As part of this research, a series of alkoxylated 6H-benzo[c]chromen-6-one derivatives were designed and synthesized. Furthermore, their biological activities were evaluated as potential PDE2 inhibitors, and the alkoxylated 6H-benzo[c]chromen-6-one derivative 1f was found to have the optimal inhibitory potential (IC50: 3.67 ± 0.47 μM). It also exhibited comparable activity in comparison to that of BAY 60-7550 in vitro cell level studies

Additional file 4 of Screening lifespan-extending drugs in Caenorhabditis elegans via label propagation on drug-protein networks

The aging-related genes of C. elegans extracted from GenAge database, together with the corresponding transcripts of each aging-related genes. (XLSX 99 kb

Adverse Effects from Clenbuterol and Ractopamine on Nematode <i>Caenorhabditis elegans</i> and the Underlying Mechanism

<div><p>In the present study, we used <i>Caenorhabditis elegans</i> assay system to investigate <i>in vivo</i> toxicity from clentuberol and ractopamine and the possible underlying mechanism. Both acute and prolonged exposures to clentuberol or ractopamine decreased brood size and locomotion behavior, and induced intestinal autofluorescence and reactive oxygen species (ROS) production. Although acute exposure to the examined concentrations of clentuberol or ractopamine did not induce lethality, prolonged exposure to 10 µg/L of clentuberol and ractopamine reduced lifespan. At relatively high concentrations, ractopamine exhibited more severe toxicity than clentuberol on nematodes. Overexpression of <i>sod-2</i> gene encoding a Mn-SOD to prevent induction of oxidative stress effectively inhibited toxicity from clentuberol or ractopamine. Besides oxidative stress, we found that clentuberol might reduce lifespan through influencing insulin/IGF signaling pathway; however, ractopamine might reduce lifespan through affecting both insulin/IGF signaling pathway and TOR signaling pathway. Ractopamine more severely decreased expression levels of <i>daf-16</i>, <i>sgk-1</i>, <i>skn-1</i>, and <i>aak-2</i> genes than clentuberol, and increased expression levels of <i>daf-2</i> and <i>age-1</i> genes at the examined concentration. Therefore, the <i>C. elegans</i> assay system may be useful for assessing the possible toxicity from weight loss agents, and clentuberol and ractopamine may induce toxicity through different molecular mechanisms.</p></div