Microplastics (MPs) are present in global indoor dust, which is an important source of MPs for humans. However, few researchers have investigated differences in the abundance and characteristics of ...MPs in dust in different indoor environments. In this study, we found that residential apartments (mean: 1174 MPs/g; n = 47) had the highest abundance of MPs in indoor dust samples, followed by offices (896 MPs/g; n = 50), business hotels (843 MPs/g; n = 53), university dormitories (775 MPs/g; n = 48), and university classrooms (209 MPs/g; n = 44). The predominant shape of MPs was fiber in most indoor dust samples. The main size fraction of the MPs in the indoor dust samples from university classrooms and business hotels was 201–500 μm, and it was 501–1000 μm in those from offices, university dormitories, and residential apartments. The main MP polymer in indoor dust samples from business hotels, university dormitories, and residential apartments was polyester, whereas those from offices and university classrooms were mainly polyethylene and polypropylene. We calculated the estimated daily intake (EDI) of MPs through the inhalation of indoor dust, and found that infants (7.4 MPs/kg bw/day) had a higher mean EDI of MPs than toddlers (1.4 MPs/kg bw/day), children (0.49 MPs/kg bw/day), adults (0.23 MPs/kg bw/day), and university students (0.22 MPs/kg bw/day). To the best of our knowledge, we are the first to report differences in MP occurrence in dust samples from different indoor environments, and our findings provide a more accurate understanding of exposure risks of MPs to humans.
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•We examined the presence of MPs in dust in different indoor environments.•Indoor dust samples from residential apartments had the highest abundance of MPs.•Fiber was the predominant shape of MPs in most indoor dust samples.•We calculated the estimated daily intake of MPs through indoor dust intake.
The unique physicochemical properties of two-dimensional (2D) graphene oxide (GO) could greatly benefit the biomedical field; however, recent research demonstrated that GO could induce in vitro and ...in vivo toxicity. We determined the mechanism of GO induced toxicity, and our in vitro experiments revealed that pristine GO could impair cell membrane integrity and functions including regulation of membrane- and cytoskeleton-associated genes, membrane permeability, fluidity and ion channels. Furthermore, GO induced platelet depletion, pro-inflammatory response and pathological changes of lung and liver in mice. To improve the biocompatibility of pristine GO, we prepared a series of GO derivatives including aminated GO (GO-NH2), poly(acrylamide)-functionalized GO (GO-PAM), poly(acrylic acid)-functionalized GO (GO-PAA) and poly(ethylene glycol)-functionalized GO (GO-PEG), and compared their toxicity with pristine GO in vitro and in vivo. Among these GO derivatives, GO-PEG and GO-PAA induced less toxicity than pristine GO, and GO-PAA was the most biocompatible one in vitro and in vivo. The differences in biocompatibility were due to the differential compositions of protein corona, especially immunoglobulin G (IgG), formed on their surfaces that determine their cell membrane interaction and cellular uptake, the extent of platelet depletion in blood, thrombus formation under short-term exposure and the pro-inflammatory effects under long-term exposure. Overall, our combined data delineated the key molecular mechanisms underlying the in vivo and in vitro biological behaviors and toxicity of pristine GO, and identified a safer GO derivative that could be used for future applications.
Short-chain chlorinated paraffins (SCCPs), which are candidate persistent organic pollutants (POPs) according to the Stockholm Convention, are of great concern because of their persistent ...bioaccumulation, long-range transport and potential adverse health effects. However, data on the endocrine-disrupting effects of SCCPs remain scarce. In this study, we first adopted two in vitro models (reporter gene assays and H295R cell line) to investigate the endocrine-disrupting effects of three SCCPs (C10-40.40%, C10-66.10% and C11-43.20%) via receptor mediated and non-receptor mediated pathway. The dual-luciferase reporter gene assay revealed that all test chemicals significantly induced estrogenic effects, which were mediated by estrogen receptor α (ERα), in the following order: C11-43.20%>C10-66.10%>C10-40.40%. Notably, C10-40.40% and C10-66.10% also demonstrated remarkable anti-estrogenic activities. Only C11-43.20% showed glucocorticoid receptor-mediated (GR) antagonistic activity, with a RIC20 value of 2.6×10−8mol/L. None of the SCCPs showed any agonistic or antagonistic activities against thyroid receptor β (TRβ). Meanwhile, all test SCCPs stimulated the secretion of 17β-estradiol (E2). Both C10-66.10% and C11-43.20% increased the production of cortisol at a high level in H295R cell lines. In order to explore the possible mechanism underlying the endocrine-disrupting effects of SCCPs through the non-receptor pathway, the mRNA levels of 9 steroidogenic genes were measured by real-time polymerase chain reaction (RT-PCR). StAR, 17βHSD, CYP11A1, CYP11B1, CYP19 and CYP21 were upregulated in a concentration-dependent manner by all chemicals. The data provided here emphasized that comprehensive assessments of the health and ecological risks of emerging contaminants, such as SCCPs, are of great concern and should be investigated further.
•All three SCCPs exert potential estrogenic activities via estrogen receptor α.•The C11-43.20% showed glucocorticoid receptor-mediated antagonistic activity.•The SCCPs disturbed the genes involved in synthesis of steroid hormones.
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Abstract
Although tremendous achievements have been made toward inertial confinement fusion, laser plasma instabilities (LPIs) remain to be an inevitable problem for current drive schemes. To ...mitigate these instabilities, significant efforts have been paid to produce high-power broadband ultraviolet lasers. However, no practical scheme has been demonstrated up to now for efficient triple-frequency conversion of broadband laser. Here we propose the design of polychromatic drivers for the generation of multicolor beams mainly based upon the optical parametric amplification, which can significantly enhance the third-harmonic conversion efficiency. Each polychromatic light has four colors of monochromatic beamlets with a full spectrum width of 3%, and the beamlet colors of any two adjacent flanges are different. The suppression effects of such polychromatic lights have been investigated via large scale particle-in-cell simulations, which indicate that more than 35% of the incident energy can be saved from the LPIs compared with monochromatic lasers for the direct-drive scheme, or high-density filled target for the indirect-drive scheme. The proposed polychromatic drivers are based on the matured technologies, and thus may pave the way towards realization of robust and high-efficiency fusion ignition.
Bisphenol analogues including bisphenol A (BPA), bisphenol AF (BPAF), bisphenol F (BPF), and bisphenol S (BPS) share similar chemical structures and endocrine disrupting effects. Their effects on ...metabolisms, however, are so far only marginally understood. In this study, NMR-based metabonomic profiles of HepG2 cell culture media and PCR array were used to assess the metabolomics disturbances and gene expression levels of HepG2 in response to four BPs (BPA, BPAF, BPF, and BPS). The results indicated that BP analogues resulted in disturbances in 7–15 metabolites that were classified as amino acid (alanine, glutamine, glutamate), intermediates and end-products in the glycolysis (pyruvate) and the tricarboxylic acid cycle (acetate, lactate). Their rank in order according to the number of metabolites and pathways was BPF > BPA > BPAF > BPS. The common disrupted pathways (pyruvate metabolism; alanine, aspartate, and glutamate metabolism) indicated enhanced glycolysis. The following glucometabolic PCR array analysis suggested that although four BPs shared the capability of disrupting glucose metabolism, they may act through different mechanisms: BPAF has increased the pyruvate kinase (PKLR) expression level, which implied enhanced glycolysis that was agreed with NMR results. The other three BP analogues, however, decreased the expression level of glucokinase (GCK) that indicated glucose sensing impairment. Our results demonstrated the potential for using metabolomic and PCR array to understand the underlying action of mechanisms and identify the potential targets for future targeted risk assessment.
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•The rank order of metabolomic disturbances of four bisphenol analogues in HepG2 cells was BPF > BPA > BPAF > BPS.•BPAF increased the pyruvate kinase (PKLR) and pyruvate level indicated enhanced glycolysis.•BPA, BPF, and BPS decreased the glucokinase (GCK) level implied an impaired glucose sensing.
The stability of Mn-promoted Ni/SiO2 catalyst for methane CO2 reforming was investigated comparatively to that of Zr-promoted Ni/SiO2. The catalysts were prepared by the same impregnation method with ...the same controlled promoter contents and characterized by TPR, XRD, TG, SEM, XPS and Raman techniques. The addition of Mn to Ni/SiO2 catalyst promoted the dispersion of Ni species, leading to smaller particle size of NiO on the fresh Ni–Mn/SiO2 catalyst and the formation of NiMn2O4, which enhanced the interaction of the modified support with Ni species. Thus, the Ni–Mn/SiO2 catalyst showed higher activity and better ability of restraining carbon deposition than Ni/SiO2 catalyst. Besides, it exhibited stable activity at reaction temperatures over the range from 600°C to 800°C. However, the introduction of Zr increased the reducibility of Ni–Zr/SiO2, and the catalyst deactivated much more dramatically when the reaction temperature decreased due to its poor ability of restraining carbon deposition, and its activity decreased monotonically with time on stream at 800°C.
Introduction of Mn to Ni/SiO2 leads to higher metal dispersion, stronger metal-support interaction, and great ability of restraining carbon deposition, keeping the Ni–Mn/SiO2 catalyst stable. Display omitted
► Ni–Mn/SiO2 catalyst exhibited good stability for CH4 reforming of CO2. ► The addition of Mn decreased the reducibility of Ni–Mn/SiO2. ► Ni–Mn/SiO2 catalyst exhibited high ability of restraining carbon deposition. ► The activity of Ni–Zr/SiO2 catalyst decreased monotonically with time on stream. ► A large mounts of carbon deposited on Ni–Zr/SiO2 catalyst.
Establishment of sister chromatid cohesion N-acetyltransferase 2 (ESCO2) is involved in the mitotic S-phase adhesins acetylation and is responsible for bridging two sister chromatids. However, ...present ESCO2 cancer research is limited to a few cancers. No systematic pan-cancer analysis has been conducted to investigate its role in diagnosis, prognosis, and effector function.
We thoroughly examined the ESCO2 carcinogenesis in pan-cancer by combining public databases such as The Cancer Genome Atlas (TCGA), Genotype-Tissue Expression Project (GTEx), UALCAN and Tumor Immune Single-cell Hub (TISCH). The analysis includes differential expression analysis, survival analysis, cellular effector function, gene mutation, single cell analysis, and tumor immune cell infiltration. Furthermore, we confirmed ESCO2's impacts on clear cell renal cell carcinoma (ccRCC) cells' proliferative and invasive capacities in vitro.
In our study, 30 of 33 cancer types exhibited considerably greater levels of ESCO2 expression in tumor tissue using TCGA and GTEx databases, whereas acute myeloid leukemia (LAML) exhibited significantly lower levels. Kaplan-Meier survival analyses in adrenocortical carcinoma (ACC), kidney chromophobe (KICH), kidney renal clear cell carcinoma (KIRC), kidney renal papillary cell carcinoma (KIRP), brain lower grade glioma (LGG), liver hepatocellular carcinoma (LIHC), lung adenocarcinoma (LUAD), mesothelioma (MESO), and pancreatic adenocarcinoma (PAAD) demonstrated that tumor patients with high ESCO2 expression have short survival periods. However, in thymoma (THYM), colon adenocarcinoma (COAD) and rectum adenocarcinoma (READ), ESCO2 was a favorable prognostic factor. Moreover, ESCO2 expression positively correlates with tumor stage and tumor size in several cancers, including LIHC, KIRC, KIRP and LUAD. Function analysis revealed that ESCO2 participates in mitosis, cell cycle, DNA damage repair, and other processes. CDK1 was identified as a downstream gene regulated by ESCO2. Furthermore, ESCO2 might also be implicated in immune cell infiltration. Finally, ESCO2'S knockdown significantly inhibited the A498 and T24 cells' proliferation, invasion, and migration.
In conclusion, ESCO2 is a possible pan-cancer biomarker and oncogene that can reliably predict the prognosis of cancer patients. ESCO2 was also implicated in the cell cycle and proliferation regulation. In a nutshell, ESCO2 is a therapeutically viable and dependable target.
The primary cilia (PC) is a microtubule-based and nonmotile organelle which protrudes from the surface of almost all mammalian cells. At present, PC has been found to be a deficiency or loss in ...multiple cancers. Restoring PC could be a novel targeting therapy strategy. Our research showed that PC was reduced in human bladder cancer (BLCA) cells, and PC deficiency promotes cell proliferation. However, the concrete mechanisms remain unknown. SCL/TAL1 interrupting locus (STIL), a PC-related protein, was screened in our previous study and could influence the cell cycle by regulating PC in tumor cells. In this study, we aimed to elucidate the function of STIL for PC to explore the underlying mechanism of PC in BLCA.
Public database analysis, western blot, and enzyme-linked immunosorbent assay (ELISA) were used to screen genes and explore gene expression alteration. Immunofluorescence and western blot were utilized to investigate PC. Wound healing assay, clone formation assay, and CCK-8 assay were used to explore cell migration, growth, and proliferation. The co-immunoprecipitation and western blot were employed to reveal the interaction of STIL and AURKA.
We found that high STIL expression is correlated with poor outcomes of BLCA patients. Further analysis revealed that STIL overexpression could inhibit PC formation, activate SHH signaling pathways, and promote cell proliferation. In contrast, STIL-knockdown could promote PC formation, inactivate SHH signaling, and inhibit cell proliferation. Furthermore, we found that the regulatory functions of STIL for PC depend on AURKA. STIL could influence proteasome activity and maintain AURKA stabilization. AURKA-knockdown could reverse PC deficiency caused by STIL overexpression for PC in BLCA cells. We observed that co-knockdown in STIL and AURKA significantly enhanced PC assembly.
In summary, our result provides a potential therapy target for BLCA based on the restoration of PC.
Human exposure to p-phenylenediamine derivatives (PPDs) may induce hepatotoxicity and altered glycolipid metabolism. Recent studies have demonstrated the wide presence of PPDs in environmental ...matrixes. However, until now, the occurrence of PPDs in tap water has not been well known. This study analyzed nine PPDs in tap water collected from Hangzhou and Taizhou, China. The results showed that seven PPDs were detected in tap water samples from Hangzhou (n = 131), with the concentration of total detected PPDs ranging from 0.29 to 7.9 ng/L (mean: 1.6 ng/L). N-(1, 3-dimethylbutyl)-N′-phenyl-p-phenylenediamine (6PPD; mean: 0.79 ng/L, <LOD−5.7 ng/L) was the predominant PPD in tap water from Hangzhou, followed by N, N′-di-2-butyl-p-phenylenediamine (44PD; 0.39 ng/L, <LOD−2.2 ng/L) and N-isopropyl-N′-phenyl-1, 4-phenylenediamine (IPPD; 0.31 ng/L, <LOD−1.4 ng/L). Five PPDs were detected in tap water collected from Taizhou (n = 30). N-phenyl-N′-cyclohexyl-p-phenylenediamine (CPPD; mean: 1.0 ng/L, <LOD−4.2 ng/L) was the predominant PPD in tap water from Taizhou, followed by 6PPD (0.93 ng/L, <LOD−2.6 ng/L) and 44PD (0.78 ng/L, <LOD−1.8 ng/L). The mean daily intake (DI) of PPDs for adults and children in Hangzhou was estimated to be 4.9–24 and 6.4–32 pg/kg bw/day, respectively. Meanwhile, the mean DI of PPDs for adults and children living in Taizhou was 11–31 and 14–40 pg/kg bw/day, respectively. To our knowledge, this study provides the first data on the occurrence of PPDs in tap water, which is vital for human exposure risk assessment.
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