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Gordon and Mollenauer (G-M) proposed in 1990 that the interplay between the nonlinear Kerr effect and amplified spontaneous emission noise can generate an enhanced level of noise and degrade the performance of optical phase-modulated systems. We systematically investigate the G-M effect in 112 Gbit/s coherent dual polarization quaternary phase shift keying (DP-QPSK) systems through comprehensive simulation. The results show that in the presence or absence of inline dispersion compensation, the G-M effect will seriously damage the system performance. Some of our important conclusions are listed as follows: with the increase in the input power into each span, the G-M effect is enhanced simultaneously; the smaller the span length, the stronger the G-M effect caused by more inter-span interaction; for non-zero dispersion-shifted fibers, different coefficient values will cause a similar amount of G-M effect penalty; by comparing the system performance with different dispersion compensation ratios, one can conclude that different residual dispersions of the same magnitude, no matter whether they are under-compensated or over-compensated, can derogate the overall system performance to a similar degree. In brief, the G-M effect cannot be ignored. We also have a short discussion on how to reduce and compensate for the G-M effect in DP-QPSK systems. [ABSTRACT FROM AUTHOR]

The article presents Engineered neutrophil-derived exosome-like vesicles for targeted cancer therapy. Topics discussed include Neutrophils are the most abundant innate immune cells in human circulation; however, their derived exosomes have been rarely studied for tumor treatment; and reported that exosomes from neutrophils (N-Ex) induce tumor cell apoptosis by delivering cytotoxic proteins and activating caspase signaling pathway.

Male accessory gland proteins (ACPs), secreted by the male accessory glands, are important components of seminal fluid proteins and play critical physiological roles in male and female adults. We previously identified a juvenile hormone-binding protein (JHBP) like protein in the male accessory glands of Bactrocera dorsalis. In this study, the open reading frame of this JHBP-like gene, which encodes 267 amino acid residues, was cloned. Phylogenetic analysis indicated that this gene belongs to a takeout gene family, and it was named Bdtakeout2. Spatio-temporal expression profiling was determined by quantitative real-time polymerase chain reaction (qRT-PCR). Bdtakeout2 was highly expressed in male accessory glands, especially in sexually mature males. Treatment with exogenous hormones significantly decreased the expression level of Bdtakeout2. Photoperiod exposure produced a relatively lower expression during the photophase and a higher expression during the scotophase. Suppression of Bdtakeout2 expression by RNA interference significantly reduced both male mating success and the fertility of mated females. The data indicate that Bdtakeout2 plays a critical role in male mating behavior and fertility. [ABSTRACT FROM AUTHOR]

We report an investigation on c-axis point-contact Andreev reflection (PCAR) spectroscopy of optimally doped BaFe1.9Ni0.1As² single crystals. The PCAR spectrum features the structures of a conductance peak with the energy scale of an electron-boson coupling mode. Quantitative analysis using a generalized Blonder-Tinkham-Klapwijk formalism with two gaps--one isotropic and another angle dependent--resolves a nodeless state in the strong-coupling limit with gap minima on the Fermi surfaces. Using the extracted superconducting energy gap value, a characteristic boson energy &OHgr;b is obtained. Our results are consistent with the pairing interaction mediated by the antiferromagnetic spin fluctuations. [ABSTRACT FROM AUTHOR]

Objective The objective of this study was to investigate the efficacy of mesenchymal stem cell (MSC) in the treatment of arthritis. Methods Mesenchymal stem cells were injected intravenously into mice with collagen-induced arthritis (CIA). Arthritic indexes were evaluated, and the levels of the proand anti-inflammatory cytokines interleukin-10 (IL-10), gamma interferon (IFN-γ)-inducible protein 10 (IP-10), chemokine (C-X-C motif) receptor 3 (CXCR3), interleukin-17A (IL-17A), and tumor necrosis factor α (TNF-α) in serum or splenic cells were determined using real-time RT-PCR, Western blotting, and enzyme-linked immunosorbent assay (ELISA). The proliferation of dendritic cell line D2SC cells was determined using ³H-TdR incorporation assay. Results Upon injection of MSCs, overall arthritis symptoms were significantly improved in the CIA mouse models as indicated by the paw edema. Consistent with this observation, serum levels of pro-inflammatory cytokine TNF-α and inflammatory cell infiltration decreased significantly 12 days after MSC injection, while the expression of anti-inflammatory cytokines IL-10, IP-10, and CXCR3 was increased in splenocytes. In addition, we provided evidence that MSCs may directly promote the proliferation of D2SC cells and the expression of IP-10 in D2SC cells in vitro. Conclusion Mesenchymal stem cells significantly enhance the efficacy of collagen-induced arthritis treatment, likely through the modulation of the expression of various cytokines. [ABSTRACT FROM AUTHOR]

Aims: To investigate human umbilical cord-derived mesenchymal stem cells (hUCMSCs) for use in the reversal of mouse hepatic injury. Methods: Human umbilical cord-derived mesenchymal stem cells, characterized by flow cytometry, were transplanted into carbon tetrachloride (CCl4)-injured mice, and then followed for determination of localization and differentiation. Reverse transcriptase-polymerase chain reaction for the human 17α gene and fluorescence in situ hybridization analysis for the human X chromosome were used to locate exogenous hUCMSCs in mouse livers. Peripheral blood and liver specimens were collected at 7, 14 and 21 days after transplantation. For evaluating the recovery of injured liver tissues, serum aminotransferase was measured, and the pathological state of the hepatocytes was assessed. Results: The hUCMSCs were positive for the human MSC-specific markers CD13, CD29, CD44, CD105 and nerve growth factor receptor, but negative for the haematopoietic lineage markers CD31, CD34, CD38, CD45 and HLA-DR. Under conditions favouring differentiation in vivo, the expression of tryptophan 2,3-dioxygenase, human alpha-fetoprotein, cytokeratin 18, fibroblast secretory protein 1 and alpha-smooth-muscle-actin was detectable after hUCMSCs administration to mice subjected to liver injury. Terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate (dUTP)-biotin nick end labelling and proliferating cell nuclear antigen staining showed that transplanted hUCMSCs could inhibit hepatocyte apoptosis and facilitate proliferation. Serum aminotransferases were decreased after transplantation of hUCMSCs into the injured mice, and hepatocyte denaturation was reduced. Conclusions: Human umbilical cord-derived mesenchymal stem cells can enhance recovery of CCl4-injured mouse liver, providing evidence that such therapy could be useful for liver disorders or injury. [ABSTRACT FROM AUTHOR]

Many insects possess a sexual communication system that is vulnerable to chemical espionage by parasitic wasps. We recently discovered that a hitch-hiking (H) egg parasitoid exploits the antiaphrodisiac pheromone benzyl cyanide (BC) of the Large Cabbage White butterfly Pieris brassicae. This pheromone is passed from male butterflies to females during mating to render them less attractive to conspecific males. When the tiny parasitic wasp Trichogramma brassicae detects the antiaphrodisiac, it rides on a mated female butterfly to a host plant and then parasitizes her freshly laid eggs. The present study demonstrates that a closely related generalist wasp, Trichogramma evanescens, exploits BC in a similar way, but only after learning. Interestingly, the wasp learns to associate an H response to the odors of a mated female P. brassicae butterfly with reinforcement by parasitizing freshly laid butterfly eggs. Behavioral assays, before which we specifically inhibited long-term memory (LTM) formation with a translation inhibitor, reveal that the wasp has formed protein synthesis-dependent LTM at 24 h after learning. To our knowledge, the combination of associatively learning to exploit the sexual communication system of a host and the formation of protein synthesis-dependent LTM after a single learning event has not been documented before. We expect it to be widespread in nature, because it is highly adaptive in many species of egg parasitoids. Our finding of the exploitation of an antiaphrodisiac by multiple species of parasitic wasps suggests its use by Pieris butterflies to be under strong selective pressure. [ABSTRACT FROM AUTHOR]

Sec14p-like lipid-binding domain (SEC14 domain) is an evolutionarily conserved protein domain often found in secretory proteins, such as Saccharomyces cerevisiae phosphatidylinositol transfer protein Sec14p, and in lipid-regulated proteins, such as GTPase-activating proteins, guanine nucleotide exchange factors, and neurofibromin. We have cloned a novel human gene, cellular retinaldehyde-binding protein-like (CRALBPL), containing SEC14 domain from the cDNA library of human fetal brain. The RT-PCR expression pattern of 16 adult human tissues indicated that CRALBPL was only expressed in brain, while it was expressed in all of seven human carcinoma cell lines we used, especially in human gastric adenocarcinoma cell line, human rhabdomyoma cell line, human hepatocellular carcinoma (HCC) cell line, and human prostatic carcinoma cell line. Further, we found that CRALBPL has a remarkably more abundant RT-PCR expression pattern in human HCC cell lines than in normal human liver cell line, and the same result was gained when RT-PCR expression patterns between human HCC specimens and normal human liver specimens were compared. We also found that CRALBPL is located mainly in cytoplasm in human liver cell line L-02, which is consistent with the common function of Sec14p-like domain family. Our results show that CRALBPL may be used as a marker for human HCCs. [ABSTRACT FROM AUTHOR]

3H-2-imino-4-methylbenzothiazoline was obtained from o-methylaniline to form 4. The yielded product 6 was confirmed by Elemental analyses, NMR, MS, IR spectra and X-ray crystallography. Compound 6, C8H8N2S, Mr=164.23, crystallized in the monoclinic space group P21/c with unit cell parameters a=4.0949(15), b=11.790(2), c=15.837(2) A˚, α=89.975(14), β=96.510(19), γ=90.09(2)°, V=759.7(3) A˚3, Z=4, Dm=1.436 Mgm−3. The intermolecular attraction of 3H-2-imino-4-methylbenzothiazoline in crystal structure is discussed. [Copyright &y& Elsevier]

Purpose: With advancements in medical imaging, more renal tumors are detected early, but it remains a challenge for radiologists to accurately distinguish subtypes of renal parenchymal tumors. We aimed to establish a novel deep convolutional neural network (CNN) model and investigate its effect on identifying subtypes of renal parenchymal tumors in T2-weighted fat saturation sequence magnetic resonance (MR) images. Methods: This retrospective study included 199 patients with pathologically confirmed renal parenchymal tumors, including 77, 46, 34, and 42 patients with clear cell renal cell carcinoma (ccRCC), chromophobe renal cell carcinoma (chRCC), angiomyolipoma (AML), and papillary renal cell carcinoma (pRCC), respectively. All enrolled patients underwent kidney MR scans with the field strength of 1.5 Tesla (T) or 3.0 T before surgery. We selected T2-weighted fat saturation sequence images of all patients and built a deep learning model to determine the type of renal tumors. Receiver operating characteristic (ROC) curve was depicted to estimate the performance of the CNN model; the accuracy, precision, sensitivity, specificity, F1-score, and area under the curve (AUC) were calculated. One-way analysis of variance and χ2 tests of independent samples were used to analyze the variables. Results: The experimental results demonstrated that the model had a 60.4% overall accuracy, a 61.7% average accuracy, and a macro-average AUC of 0.82. The AUCs for ccRCC, chRCC, AML, and pRCC were 0.94, 0.78, 0.80, and 0.76, respectively. Conclusion: Deep CNN model based on T2-weighted fat saturation sequence MR images was useful to classify the subtypes of renal parenchymal tumors with a relatively high diagnostic accuracy. [ABSTRACT FROM AUTHOR]

Acquired lymphedema is a complex disease caused by cancer treatment or parasitic infection and few effective treatments are available for lymphedema.1-3 It is urgently needed to develop new experimental approaches and therapeutic strategies.3 In this study, we address a new role and mechanism of MSC-ex (human umbilical cord Wharton's jelly mesenchymal stem cells derived exosome) in lymphedema treatment. MSC-ex treatment promoted lymphatic drainage in lymphedema mice as injected methylene blue across the site of incision at week 6, which was not found in PBS treated mice (Figure 1J). As lymphangiogenesis is crucial in lymphedema development after lymphatic ablation,4,5 we analyzed the lymphatic anatomy and lymphangiogenesis in MSC-ex treated animals. [Extracted from the article]

Objective: To investigate specific muscle pathologies of different kinds of myositis-specific autoantibodies (MSAs) in idiopathic inflammatory myopathy (IIM) patients. Methods: One hundred eleven Chinese patients from Xiangya Hospital, Central South University diagnosed with IIMs according to European Neuromuscular Centre (ENMC) criteria were included. Clinical manifestation, myositis-specific autoantibodies, and histologic findings were evaluated to explore the pattern of necrosis, regeneration, and perifascicular atrophy, inflammatory cells in IIM patients with different MSAs. Results: Anti-SRP group has the lowest muscle strength scores, the highest creatine kinase levels, the most severe degree of necrosis and regeneration (1.90[0.80–3.95], 1.00[0.30–1.71]), and the lowest positive rate of MHC-I staining (35.71%). The anti-MDA5 group demonstrates the mildest pathological changes, with the fewest necrotic and regenerated muscle fibers (0.00[0.00–0.50], 0.00[0.00–0.00]), and the fewest inflammatory cell infiltration, and the highest muscle strength scores. The anti-NXP2 group has the most frequent inflammatory infiltrates, especially CD4+ T cells (31.14[15.00–39.00]). The patients with anti-NXP2 and the anti-TIF1γ antibodies show higher frequency of punched-out fibers (1.50[0.00–3.70], 0.00[0.00–1.00]) and perifascicular atrophy (71.43%, 55.56%). As for anti-synthetase antibodies (ASAs), the anti-Jo-1 group shows the most frequent rate of perifascicular necrosis (60%), while other ASA groups do not show perifascicular necrosis. Conclusions: Of the MSAs, the anti-SRP antibody leads to the most severe muscle involvement, while the anti-MAD5 antibody the mildest. The anti-NXP2 and anti-TIF1γ groups have the most typical "DM" pathology. Key Points • Anti-SRP group shows severe muscle pathology while anti-MDA5 group shows the mildest. • Anti-NXP2 group has the most frequent inflammatory infiltrates. Pouch-out fibers and perifascicular atrophy are more prevalent in anti-NXP2 and anti-TIF1γ groups. • Anti-Jo-1 group is often accompanied by perifascicular necrosis, while other anti-synthetase antibody groups are not. [ABSTRACT FROM AUTHOR]

• Inhibition of starch digestion in nonionic steric emulsifier Pluronics was explored. • The role of hydrophobic domain of both α-amylase and substrates was disclosed. • Pluronic causes more changes in amylase structure than it affects starch structure. • Design of amylase inhibitors can be considered from changing hydrophobic groups. The physicochemical mechanism of starch digestion is very complicated since it may be affected by the non-valence interactions of the amylase inhibitor with the substrate or the enzyme. The role of hydrophobic interaction in the process of starch digestion is not clear. In this study, pluronics (PLs) with different hydrophobicity were used as model amphiphilic compounds to study their inhibition on starch digestion using multi-spectroscopic methods. The results showed that the hydrophobic nature of PLs changed starch structure, but it had a greater effect on the structure of α-amylase by exposing more tryptophan residues and increasing α-helix and β-sheet contents. Further investigation by using different chain-length fatty acids confirmed the results. The finding in this study is informative to design and fabricate α-amylase inhibitors for controlling starch digestion at the molecular level. [ABSTRACT FROM AUTHOR]

The Tibetan Plateau is the source of most of Asia's major rivers and has been called the Asian Water Tower. Detailed knowledge of its hydrogeology is paramount to enable the understanding of groundwater dynamics, which plays a vital role in headwater areas like the Tibetan Plateau. Nevertheless, due to its remoteness and the harsh environment, there is a lack of field survey data to investigate its hydrogeology. In this study, borehole core lithology analysis, altitude survey, soil thickness measurement, hydrogeological survey, and hydrogeophysical surveys (e.g., Magnetic Resonance Sounding – MRS, Electrical Resistivity Tomography – ERT, and Transient Electromagnetic – TEM) were conducted in the Maqu catchment within the Yellow River Source Region (YRSR). The soil thickness measurements were done in the western mountainous area of the catchment, where hydrogeophysical surveys were difficult to be carried out. The results indicate soil thicknesses are within 1.2 m in most cases, and the soil thickness decreases as the slope increases. The hydrogeological survey reveals that groundwater flows from the west to the east, recharging the Yellow River. The hydraulic conductivity ranges from 0.2 m/d to 12.4 m/d. The MRS soundings results, i.e., water content and hydraulic conductivity, confirmed the presence of unconfined aquifer in the flat eastern area. The depth of the Yellow River deposits was derived at several places in the flat eastern area based on TEM results. These survey data and results can be used to develop integrated hydrological modeling and water cycle analysis to improve a full–picture understanding of the water cycle at the Maqu catchment in the YRSR. The raw data set is freely available at https://doi.org/10.17026/dans-z6t-zpn7 (Li et al., 2020). [ABSTRACT FROM AUTHOR]

Background: Long non-coding RNAs (lncRNAs) are involved in many fundamental biological processes, such as transcription regulation, protein degradation, and cell differentiation. Information on lncRNA in the melon fly, Zeugodacus cucurbitae (Coquillett) is currently limited. Results: We constructed 24 RNA-seq libraries from eight tissues (midgut, Malpighian tubules, fat body, ovary, and testis) of Z. cucurbitae adults. A total of 3124 lncRNA transcripts were identified. Among those, 1464 were lincRNAs, 1037 were intronic lncRNAs, 301 were anti-sense lncRNAs, and 322 were sense lncRNAs. The majority of lncRNAs contained two exons and one isoform. Differentially expressed lncRNAs were analyzed between tissues, and Malpighian tubules versus testis had the largest number. Some lncRNAs exhibited strong tissue specificity. Specifically expressed lncRNAs were identified and filtered in tissues of female and male Z. cucurbitae based on their expression levels. Four midgut-specific lncRNAs were validated by quantitative real-time polymerase chain reaction (RT-qPCR), and the data were consistent with RNA-seq data. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses of targets of midgut-specific lncRNAs indicated an enrichment of the metabolic process. Conclusions: This was the first systematic identification of lncRNA in the melon fly. Expressions of lncRNAs in multiple adult tissues were evaluated by quantitative transcriptomic analysis. These qualitative and quantitative analyses of lncRNAs, especially the tissue-specific lncRNAs in Z. cucurbitae, provide useful data for further functional studies. [ABSTRACT FROM AUTHOR]

We report the observation of a π-type dipole-bound state (π-DBS) in cryogenically cooled deprotonated 9-anthrol molecular anions (9AT-) by resonant two-photon photoelectron imaging. A DBS is observed 191 cm-1 (0.0237 eV) below the detachment threshold, and the existence of the π-DBS is revealed by a distinct (s+d)-wave photoelectron angular distribution. The π-DBS is stabilized by the large anisotropic in-plane polarizability of 9AT. The population of the dipole-forbidden π-DBS is proposed to be via a nonadiabatic coupling with the dipole-allowed σ-type DBS mediated by molecular rotations. [ABSTRACT FROM AUTHOR]

Based on the evaluation data of groundwater resources and the demand for water resources in the construction planning of Ningdong Energy and Chemical Base, a joint water supply plan for surface water and groundwater was proposed, and a linear programming model was used to optimize the joint water supply plan, which determined the actual quota and water supply route in the water supply plan. The results showed that Taole riverside water source could supply 0.065 x 108 m³/a of water to Pingluo Fine Chemical Base; Luotuojing emergency water source can could 0.019 x 108 m³/a of water to Hengcheng and Yuanyanghu Industrial and Mining Area; the No. 2 and No. 3 alternative water sources of Wuzhong Plain could supply 0.089 x 108 m³/a and 0.067 x 108 m³/a of water to Lingwu Industrial and Mining Area; No. 1 water source of Daquan area could supply 0.054 x 108 m³/a of water to Majiatan and Jijiajing Industrial and Mining Area in the south. According to the total water supply volume of 0.294 x 108 m³/a and the optimal water supply route, the groundwater quota is only 3.136 x 108 m³/a, which can not only meet the demand for water resources of the Ningdong Energy and Chemical Industry Base in 2020, but also can maximize the socio-economic and environmental benefits. The research could provide foundation basis for the economic and efficient utilization of water resources in the Base, and also provide references for the rational utilization of water resources in the industrial base of the arid area. [ABSTRACT FROM AUTHOR]

Age-associated diseases, including vascular diseases, are on the rise with the increase in the aging population. However, the mechanisms of aging and age-associated vascular dysfunction remain to be fully elucidated. Replicative senescence of vascular smooth muscle cells (VSMCs) contributes to aging as well as age-associated vascular diseases. Rapamycin may delay aging-associated diseases via inhibition of the mammalian target of rapamycin (mTOR), but its role in VSMC aging has remained elusive. The present study investigated the involvement of mTOR signaling in replicative senescence of VSMCs. Replicative senescence was induced in human VSMCs by extended passages and identified by assessing the cell morphology, senescence-associated β-galactosidase activity, and p53 and p21 protein expression. Protein expression and phosphorylation were determined by western blot analysis. Significant senescence of VSMCs was observed in cells subjected to extended passaging (until passage 15). Significant decreases in adenosine monophosphate-activated protein kinase (AMPK)/tuberous sclerosis complex 2 (TSC2) phosphorylation, but significant increases in mTOR/ribosomal protein S6 kinase 1 (S6K1) phosphorylation, were observed in cells with replicative senescence compared with those in young cells. Pre-treatment of VSMCs with AMPK activator and mTOR inhibitor delayed replicative senescence and reversed changes in AMPKα, TSC2, mTOR and S6K1 phosphorylation in senescent VSMCs. The AMPK/TSC2/mTOR/S6K1 signaling axis was found to have an important role in regulating replicative senescence of human VSMCs. [ABSTRACT FROM AUTHOR]

Composited fibrous membrane has been demonstrated as a type of versatile and efficient photothermal material to produce fresh water by solar thermal desalination, but still suffers from some shortages such as weak mechanical property for reusability and insufficient investigations on the microstructure regulation for higher evaporation performance. In this work, a self-supported carbon black/polyacrylonitrile (CB/PAN) membrane with irregular patterns was facilely manufactured by simple hot-pressing (hp- CB /PAN) for highly efficient solar thermal evaporation. The hot-pressing induces the densification of the nanofibrous membrane and melt adhesion of partial membrane surface, leading to significant increase of the mechanical property and certain improvement of water diffusion, but no detected change of the nanofibrous components. Moreover, the hp-CB/PAN possesses optical absorption of 99.1% over the entire wavelength range of 250–2500 nm. Accordingly, the hp-CB/PAN exhibits an excellent evaporation rate of 1.33 kg m−2 h−1 and a superior photothermal conversion efficiency of 86% under one sun illumination (1000 W m−2), which are much higher than those of 1.27 kg m−2 h−1 and 82.8% for CB/PAN. The obtained hp-CB/PAN can also be utilized for purifying organic polluted solution and repeatedly solar thermal evaporation without attenuation of the evaporation performance. A self-supporting carbon black/polyacrylonitrile membrane with irregular patterns was facilely manufactured by simple hot-pressing for highly efficient solar thermal evaporation. [Display omitted] • Patterned free-standing nanofibrous membrane was constructed by hot-pressing. • Enhanced mechanical and capillary force were achieved after hot-pressing. • Hot-pressed membrane exhibits improved solar evaporation performance. [ABSTRACT FROM AUTHOR]

Secreted effectors from Magnaporthe oryzae play critical roles in the interaction with rice to facilitate fungal infection and disease development. M. oryzae-secreted protein MoHrip1 can improve plant defense as an elicitor in vitro, however, its biological function in fungal infection is not clear. In this study, we found that the expression of mohrip1 was significantly induced in the stages of fungal penetration and colonization. Although dispensable for the growth and conidiation, MoHrip1 was necessary for the full virulence of M. oryzae. Deletion of mohrip1 remarkably compromised fungal virulence on rice seedlings and even on rice leaves with wounds. Rice sheath inoculation assay further demonstrated the defects of mohrip1-deleted mutants on penetration and proliferation in rice cells. Additionally, compared with WT and complementation strain, the inoculation of mohrip1-deleted mutants induced a higher expression of specific defense related genes and a higher production of specific defensive compounds in rice leaves. These data collectively indicated that MoHrip1 is necessary for fungal penetration and invasive expansion, and further full virulence of rice blast fungus. [ABSTRACT FROM AUTHOR]

Grain growth in porous ceramics is a complex process due to the variety of interactions between pores and grains. In this study, the pore deformation and grain boundary migration during porous ceramic sintering are simulated by the phase-field method, and the variety of diffusions during sintering is considered. Pores of different shapes and sizes are induced into the simulations to investigate the grain boundary migration and pore deformations during grain growth. Simulation results indicate that the porous microstructure is determined by the contacting mode between pore surface and grain boundaries, which is in good agreement with experimental observations. The efficiency of the grain boundary migration is analyzed via calculating the forces applied on the interfaces between grains and pores, and the mechanism of the pore deformation during grain boundary migration is discussed. Therefore, controlling the grain-pore microstructure by adjusting the synthesis process is essential to reach the desired mechanical and physical properties of sintered materials. [ABSTRACT FROM AUTHOR]

The pH value of oil acidized wastewater is relatively low (pH = 6.1), which seriously affects the flocculation of polyacrylamide (PAM). NaOH was used to adjust the pH value, but the maximum was only 7.5. The regulation was limited as the Ca2þ in aqueous phase up to 1,350 mg L-1 consumed OH-. A novel formulation of Na2CO3 þ PAM was proposed to form CaCO3 floc core to facilitate PAM coagulation. When the concentration was above 400 mg L-1, the PAM precipitation tended to be maximum, followed by NaOH adjustment of pH to 8.0 that could enhance PAM flocculation successively. The sewage sludge (SS) remained and residue oil reduced to 25 mg L-1 and 34 mg L-1 respectively. The analysis of the species and composition of fatty acids indicated that the coagulation-flocculation selectively effected the sedimentation of saturated fatty acids (SAT). This provides a new idea for recovery of high value-added residual oil. The optimal additive of Na2CO3 is expected as promising coagulant aid to improve the PAM coagulation-flocculation of oil acidized wastewater. [ABSTRACT FROM AUTHOR]

Objectives: Long noncoding RNAs (lncRNAs) play important roles in cancer development and progression. The deregulated expression of LINC00978 has been reported in human cancers. However, the expression pattern and biological roles of LINC00978 in gastric cancer (GC) remain unclear. In this study, we investigated the potential roles and clinical value of LINC00978 in gastric cancer. Materials and methods: QRT-PCR was performed to investigate the expression of LINC00978 in gastric cancer cell lines, tissues and serum samples. Cell counting, colony formation, transwell migration and matrigel invasion assays were performed to determine the effects of shRNA-mediated knockdown of LINC00978 on gastric cancer cell functions. In vivo tumour growth assay was also conducted. Flow cytometry, immunohistochemistry, western blot and qRT-PCR were used for potential mechanism study. Results: LINC00978 expression level was elevated in GC tumour tissues, serum samples and cell lines. The expression level of LINC00978 was significantly correlated with tumour size (P = 0.02), lymphatic metastasis (P = 0.009) and TNM stage (P = 0.009). LINC00978 knockdown inhibited the proliferation of GC cells by suppressing cell cycle progression and inducing apoptosis. LINC00978 knockdown also inhibited the migration and invasion of GC cells. In addition, LINC00978 knockdown inhibited the activation of TGF-β/ SMAD signalling pathway and the process of epithelial-mesenchymal transition (EMT) in GC cells. Moreover, the in vivo tumorigenicity of LINC00978 knockdown GC cells in mice was significantly decreased. Conclusions: LINC00978 promotes gastric cancer progression and may serve as a potential biomarker for GC. [ABSTRACT FROM AUTHOR]

CircRNAs are a class of RNA molecules that structurally form closed loops. CircRNAs are abundant in eukaryotic transcripts and show certain levels of tissue and cell specificity. CircRNAs have been suggested to regulate gene expression at transcriptional, post-transcriptional, and translational levels. An increasing number of studies have shown that circRNAs play important roles in the development and progression of diseases including cancer. In particular, circRNAs have shown great potential in cancer diagnosis, prognosis, and therapy. In this review, we provide an overview of the biogenesis and characteristics of circRNAs, succinctly describe their functions, and comprehensively discuss about the recent advances in the roles of circRNAs in cancer with an emphasis on their clinical values. [ABSTRACT FROM AUTHOR]

Non-noble metal-based heterostructures have emerged as a promising strategy to construct high-efficient electrocatalysts for the Oxygen evolution reaction. Herein, we reported a three-dimensional core-shell heterostructures of NiTe/NiCo-LDH (NiCo layered double hydroxides) on the Ni foam to resolve the low electronic conductivity and self-aggregation of NiCo-LDH. This NiTe/NiCo-LDH electrocatalyst could be prepared from a two-step reaction as a hydrothermal reaction and electrodeposition approach. Benefiting from the existence of strong interface effects between the NiTe nanorod core and NiCo-LDH nanosheet shell, the NiTe/NiCo-LDH electrocatalyst exhibited superior activity for the Oxygen evolution reaction at a current density of 100 mA cm−2 with an overpotential of 376 mV in 1.0 M KOH solution, which was significantly smaller than that of a single component of NiTe (586 mV), NiCo-LDH (410 mV) and commercial RuO 2 (428 mV). Furthermore, the NiTe/NiCo-LDH catalyst indicated long-term stability after 24 h continuous working. Density functional theory computations unveil that the heterostructures modified the original electronic structures and weakened the atomic interaction in the LDH layers, which have effectively adjusted the d -band center of the catalytic active Co sites to the Fermi level. This work demonstrated an effective strategy of interfacial engineering to optimize electron transfer to boost Oxygen evolution reaction performance. [Display omitted] • Three-dimensional (3D) core-shell heterostructure of NiTe/NiCo-LDH on the NF is synthesized. • NiTe/NiCo-LDH electrocatalyst showed extraordinary OER activity and stability under alkaline condition. • The outstanding OER performance is mainly attributed to the synergetic effect between NiTe core and NiCo-LDH shell. • OER improvement mechanism is clarified through the experiment and theoretical calculation. [ABSTRACT FROM AUTHOR]

Background: The administration of cisplatin is limited due to its nephrotoxic side effects, and prevention of this nephrotoxicity of cisplatin is difficult. Mesenchymal stem cell (MSC)-derived exosomes have been implicated as a novel therapeutic approach for tissue injury. In this study, we demonstrated that the pretreatment of human umbilical cord MSC-derived exosomes (hucMSC-Ex) can prevent the development of cisplatin-induced renal toxicity by activation of autophagy in vitro and in vivo. Methods: In vitro, rat renal tubular epithelial (NRK-52E) cells were pre-incubated with exosomes from hucMSC or HFL1 (human lung fibroblast cells; as control) for 30 min, and 3-methyladenine (an autophagic inhibitor) and rapamycin (an autophagic inducer) for 1 h before cisplatin treatment for 8 h, respectively. Cells were harvested for apoptosis assay, enzyme-linked immunosorbent assay (ELISA), Western blot, and quantitative real-time polymerase chain reaction (qRT-PCR). In vivo, we constructed cisplatin-induced acute kidney injury rat models. Prior to treatment with cisplatin for 0.5 h, hucMSC-Ex or HFL1-Ex were injected into the kidneys via the renal capsule. 3-methyladenine and rapamycin were injected under the kidney capsule before hucMSC-Ex. All animals were sacrificed at 3 days after cisplatin injection. Renal function, Luminex assay, tubular apoptosis and proliferation, and autophagy response were evaluated. Results: hucMSC-Ex inhibited cisplatin-induced mitochondrial apoptosis and secretion of inflammatory cytokines in renal tubular epithelial cells in vitro. hucMSC-Ex increased the expression of the autophagic marker protein LC3B and the autophagy-related genes ATG5 and ATG7 in NRK-52E cells. Rapamycin mimicked the effects of hucMSC-Ex in protecting against cisplatin-induced renal injury, while the effects were abrogated by the autophagy inhibitor 3-methyladenine in the animals. Conclusions: Our findings indicate that the activation of autophagy induced by hucMSC-Ex can effectively relieve the nephrotoxicity of cisplatin. Therefore, pre-treatment of hucMSC-Ex may be a new method to improve the therapeutic effect of cisplatin. [ABSTRACT FROM AUTHOR]

Background: Overexpression of cyclin D1 dependent kinases 4 and 6 (CDK4/6) is a common feature of many human cancers including leukemia. LEE011 is a novel inhibitor of both CDK4 and 6. To date, the molecular function of LEE011 in leukemia remains unclear. Methods: Leukemia cell growth and apoptosis following LEE011 treatment was assessed through CCK-8 and annexin V/propidium iodide staining assays. Cell senescence was assessed by β-galactosidase staining and p16INK4a expression analysis. Gene expression profiles of LEE011 treated HL-60 cells were investigated using an Arraystar Human LncRNA array. Gene ontology and KEGG pathway analysis were then used to analyze the differentially expressed genes from the cluster analysis. Results: Our studies demonstrated that LEE011 inhibited proliferation of leukemia cells and could induce apoptosis. Hoechst 33,342 staining analysis showed DNA fragmentation and distortion of nuclear structures following LEE011 treatment. Cell cycle analysis showed LEE011 significantly induced cell cycle G1 arrest in seven of eight acute leukemia cells lines, the exception being THP-1 cells. β-Galactosidase staining analysis and p16INK4a expression analysis showed that LEE011 treatment can induce cell senescence of leukemia cells. LncRNA microarray analysis showed 2083 differentially expressed mRNAs and 3224 differentially expressed lncRNAs in LEE011-treated HL-60 cells compared with controls. Molecular function analysis showed that LEE011 induced senescence in leukemia cells partially through downregulation of the transcriptional expression of MYBL2. Conclusions: We demonstrate for the first time that LEE011 treatment results in inhibition of cell proliferation and induction of G1 arrest and cellular senescence in leukemia cells. LncRNA microarray analysis showed differentially expressed mRNAs and lncRNAs in LEE011-treated HL-60 cells and we demonstrated that LEE011 induces cellular senescence partially through downregulation of the expression of MYBL2. These results may open new lines of investigation regarding the molecular mechanism of LEE011 induced cellular senescence. [ABSTRACT FROM AUTHOR]

Mesenchymal stem cells (MSCs) are attractive seed cells for immunotherapy, tissue engineering and regenerative medicine due to their self-renewal and multidirectional differentiation abilities, diverse immunoregulatory functions and ease of isolation from a wide range of tissues. MSCs exert their immunoregulatory effect on immune cells via cell-to-cell contact and paracrine mechanisms. In turn, MSCs can also be modulated by immune cells. Macrophages are constantly present in the mucosa of the intestinal tract of mammals and play an important role in the development and progression of inflammatory bowel disease (IBD), a chronic and recurrent inflammatory disease of the gastrointestinal tract characterized by idiopathic mucosal inflammation. The increased morbidity and mortality of IBD have made it a disease hard to cure in the clinic. MSCs have emerged as an important tool for IBD therapy due to their abilities to differentiate into enterocyte-like cells and regulate inflammatory cells, especially macrophages. In this review, we discuss the recent advances in the interaction between MSCs and macrophages in diseases, with an emphasis on IBD. We propose that an optimized MSC-based therapy would provide a novel strategy for the treatment of IBD and the prevention of IBD-associated colorectal cancer (CRC). [ABSTRACT FROM AUTHOR]

Vascular aging, a specific type of organic aging, is related to age-dependent changes in the vasculature, including atherosclerotic plaques, arterial stiffness, fibrosis, and increased intimal thickening. Vascular aging could influence the threshold, process, and severity of various cardiovascular diseases, thus making it one of the most important risk factors in the high mortality of cardiovascular diseases. As endothelial cells (ECs) and vascular smooth muscle cells (VSMCs) are the main cell biological basis of these pathology changes of the vasculature, the structure and function of ECs and VSMCs play a key role in vascular aging. MicroRNAs (miRNAs), small noncoding RNAs, have been shown to regulate the expression of multiple messenger RNAs (mRNAs) posttranscriptionally, contributing to many crucial aspects of cell biology. Recently, miRNAs with functions associated with aging or aging-related diseases have been studied. In this review, we will summarize the reported role of miRNAs in the process of vascular aging with special emphasis on EC and VSMC functions. In addition, the potential application of miRNAs to clinical practice for the diagnosis and treatment of cardiovascular diseases will also be discussed. [ABSTRACT FROM AUTHOR]

Mesenchymal stem cells (MSCs) are a component of the tumor microenvironment and can promote the development of gastric cancer through paracrine mechanism. However, the effects of MSC-exosomes (MSC-ex) on gastric cancer are less clear. The present study reported that MSC-ex promoted the proliferative and metastatic potential of gastric cancer cells ex vivo. It was found that MSC-ex enhanced the migration and invasion of HGC-27 cells via the induction of the epithelial-mesenchymal transition. MSC-ex increased the expression of mesenchymal markers and reduced the expression of epithelial markers in gastric cancer cells. MSC-ex also enhanced the tumorigenicity of gastric cancer cells ex vivo. MSC-ex induced the stemness of gastric cancer cells. The expression of octamer-binding transcription factor 4, ex determining region Y-box 2 and Lin28B significantly increased in gastric cancer cells treated with MSC-ex. The present study further demonstrated that MSC-ex elicited these biological effects predominantly via the activation of the protein kinase B signaling pathway. Taken together, the present findings provided novel evidence for the role of MSC-ex in gastric cancer and a new opportunity for improving the efficiency of gastric cancer treatment by targeting MSC-ex. [ABSTRACT FROM AUTHOR]

A correction to the article "Lipopolysaccharide-pretreated mesenchymal stem cell-conditioned medium optimized with 10 kDa filter attenuates the injury of H9c2 cardiomyocytes in a model of hypoxia/reoxygenation" that was published in a 2022 issue is presented.

Background aims. Mounting evidence shows that non-cell-based transplantation of exosomes derived from mesenchymal stromal cells (MSCs) has more potential protective and reparative effects than MSCs have. However, whether it is safe to transplant MSC exosomes into tissues is still not clear. In this study, we evaluated the safety of transplantation of exosomes derived from human umbilical cord MSCs (hucMSC exosomes). Methods. hucMSC exosomes were incubated with the cardiac blood from a healthy rabbit, and hemolysis was observed. For analysis of vascular and muscle stimulation, pyrogen, systemic anaphylaxis and hematology indexes, hucMSC exosomes were given to rabbits, guinea pigs and rats. The histological changes in the vascular and muscle sites of injection in rabbits were analyzed by hematoxylin and eosin staining. Allergy symptoms in guinea pigs and rectal temperature of rabbits were observed and recorded. To study safety in vivo, hucMSC exosomes were infused intravenously into rats with acute myocardial infarction. Rats' weight was measured and tail vein blood was collected to evaluate liver and renal function. Results. hucMSC exosomes had a protective effect on weight loss and had no adverse effects on liver or renal function. Other detections, such as hemolysis, vascular and muscle stimulation, systemic anaphylaxis, pyrogen and hematology indexes, also showed that hucMSC exosomes were applicable. Conclusions. hucMSC exosomes are well tolerated in animal models. This study provides evidence for the safety of intravenous infusion in future clinical therapy. [ABSTRACT FROM AUTHOR]

Chronic inflammation has a decisive role in tumorigenesis, particularly in gastric carcinogenesis. The CC chemokine ligand 2 (CCL2), an important inflammatory cytokine, is involved in the initiation, development and progression of various types of cancer. However, the role of CCL2 in gastric cancer remains to be elucidated. The present study demonstrated that recombinant CCL2 stimulation caused no effect on the morphology, proliferation and migration of human GES-1 gastric mucosa epithelial cells, in which the protein expression of CC-chemokine receptor 2 (CCR2) was markedly low. However, the expression of CCR2 was significantly upregulated in the GES-1 cells following pretreatment with the chemical carcinogen, N-methyl-N-nitro-N'-nitrosoguanidine (MNNG), for 12 h or transformed with MNNG (MC cells). The present study used CCL2 to stimulate MNNG pretreated GES-1 cells and MC cells, and demonstrated that CCL2 clearly promoted their migration and the epithelial-mesenchymal transition (EMT). However, no effect was observed on the proliferative ability of the cells. Taken together, these findings suggested that the CCL2/CCR2 chemokine signaling may regulate the EMT in gastric epithelial cells and resulted in gastric carcinogenesis in response to the intake of the carcinogen, MNNG. [ABSTRACT FROM AUTHOR]

Background: Emerging evidence indicates that inappropriate cell-cell fusion might contribute to cancer progression. Similarly, mesenchymal stem cells (MSCs) can also fuse with other cells spontaneously and capable of adopting the phenotype of other cells. The aim of our study was to investigate the role of MSCs participated cell fusion in the tumorigenesis of gastric cancer.Methods: We fused human umbilical cord mesenchymal stem cells (hucMSCs) with gastric cancer cells in vitro by polyethylene glycol (PEG), the hybrid cells were sorted by flow cytometer. The growth and migration of hybrids were assessed by cell counting, cell colony formation and transwell assays. The proteins and genes related to epithelial- mesenchymal transition and stemness were tested by western blot, immunocytochemistry and real-time RT-PCR. The expression of CD44 and CD133 was examined by immunocytochemistry and flow cytometry. The xenograft assay was used to evaluation the tumorigenesis of the hybrids.Results: The obtained hybrids exhibited epithelial- mesenchymal transition (EMT) change with down-regulation of E-cadherin and up-regulation of Vimentin, N-cadherin, α-smooth muscle actin (α-SMA), and fibroblast activation protein (FAP). The hybrids also increased expression of stemness factors Oct4, Nanog, Sox2 and Lin28. The expression of CD44 and CD133 on hybrid cells was stronger than parental gastric cancer cells. Moreover, the migration and proliferation of heterotypic hybrids were enhanced. In addition, the heterotypic hybrids promoted the growth abilities of gastric xenograft tumor in vivo.Conclusions: Taken together, our results suggest that cell fusion between hucMSCs and gastric cancer cells could contribute to tumorigenic hybrids with EMT and stem cell-like properties, which may provide a flexible tool for investigating the roles of MSCs in gastric cancer. [ABSTRACT FROM AUTHOR]

A mortality rate higher than 90 % was observed in a larva-rearing facility for Pacific cod, Gadus macrocephalus, in China. Larvae showing clinical signs of infection were collected. Initial suspicion of nervous necrosis virus (NNV) infection was confirmed by sequencing, absolute quantification real-time PCR (A-qPCR), and electron microscopy. The nucleotide sequence of RNA2 was 1,375 bases long (GenBank no. KM576685), coding for a single ORF corresponding to the capsid protein from residues 21 to 1034. Phylogenetic analysis of the capsid protein sequence showed that PCNNV belongs to the barfin flounder NNV (BFNVV) genotype. An amino acid sequence alignment revealed 39 differences between the cold- and warm-resistant viral groups, suggesting that PCNNV evolved under temperature selection. The 3-D structure of the predicted capsid protein was modeled to identify potential epitopes, and the gene was expressed in Escherichia coli, yielding a protein with a molecular mass of 55 kDa. During PCNNV outbreaks, the viral copy number was found to reach 10 per ng of total RNA, which could be considered the lethal copy number of NNV in cod. The gonads, eggs, fertilized eggs and asymptomatic cod fry were all positive for PCNNV, indicating viral vertical transmission as the main source of the viral load. The amount of virus in the apparent healthy fry or survivors seemed to decrease gradually with development. These results might lead to efficient diagnostic methods to help farmers select NNV-free broodfish for cod breeding. [ABSTRACT FROM AUTHOR]

Exosomes have emerged as a novel mode of intercellular communication. Exosomes can shuttle bioactive molecules including proteins, DNA, mRNA, as well as non-coding RNAs from one cell to another, leading to the exchange of genetic information and reprogramming of the recipient cells. Increasing evidence suggests that tumor cells release excessive amount of exosomes, which may influence tumor initiation, growth, progression, metastasis, and drug resistance. In addition, exosomes transfer message from tumor cells to immune cells and stromal cells, contributing to the escape from immune surveillance and the formation of tumor niche. In this review, we highlight the recent advances in the biology of exosomes as cancer communicasomes. We review the multifaceted roles of exosomes, the small secreted particles, in communicating with other cells within tumor microenvironment. Given that exosomes are cell type specific, stable, and accessible from body fluids, exosomes may provide promising biomarkers for cancer diagnosis and represent new targets for cancer therapy. [ABSTRACT FROM AUTHOR]

The fragile histidine triad (FHIT) gene is known to be a tumor suppressor gene and the abnormal methylation of FHIT has been identified in leukemia and several solid tumors. The transformation of the tumor F6 cell line from human fetal mesenchymal stem cells (FMSCs) was first reported in a previous study that also identified the presence of a population of cancer stem cells in the F6 cell line. However, the existence of the epigenetic changes during the transformation process have yet to be elucidated. To confirm the role of the FHIT gene in the transformation process of FMSC, the expression level and methylation status of the FHIT gene was examined in F6 tumor cells and FMSCs. Additionally, the alteration in cell morphology, the cell cycle and apoptosis in F6 cells following 5-Aza-CdR treatment was assessed. It was found that the FHIT gene was expressed in FMSCs, but not in F6 cells. The methylation-specific PCR results demonstrated that the promoter methylation of FHIT genes existed in the F6 cell line. Subsequent to treatment with 5-Aza-CdR the expression of FHIT genes was restored in F6 cells. In addition, the morphology of F6 cells was altered, and the cell cycle was arrested in the G2 phase, with the initiation of apoptosis. Overall, the present findings demonstrated that the FHIT gene was methylated in F6 cells and demethylation treatment lead to changes in the biological characteristics, thereby promoting the apoptosis of F6 cells. FHIT gene methylation may be one of the molecular events involved in the development and transformation of FMSCs into F6 tumor cells. [ABSTRACT FROM AUTHOR]

Mortality (>90%) is a big concern in larval rearing facilities of Pacific cod, Gadus macrocephalus , limiting its culture presently still in the experimental stages. Understanding the immune system development of G. macrocephalus is crucial to optimize the aquaculture of this species, to improve the use of economic resources and to avoid abuse of antibiotics. For the transcriptome analysis, using an Illumina sequencing platform, 61,775,698 raw reads were acquired. After a de novo assembly, 77,561 unigenes were obtained. We have classified functionally these transcripts by Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG). 27 genes mainly related to hematopoietic or lymphoid organ development and somatic diversification of immune receptors have been reported for the first time in Pacific cod, and 14 Ig heavy chain ( μ chain) locuses were assembled using Trinity. Based on our previous achievement, we have chosen Rag1 and Igμ as immune system development biomarkers. Full length cDNA of Rag1 and Igμ as biomarkers were obtained respectively using RACE PCR. Concerning Rag1 , the deduced amino acid of Rag1 and protein immunodetection revealed a Rag1 isoform of 69 kDa, significantly different from other fish orthologs, such as Oncorhynchus mykiss (121 kDa). Phylogenetic analysis reveals a unique immune system for the Gadus genre, not exclusive for Atlantic cod, among vertebrates. Meanwhile, full length cDNA of Igμ included an ORF of 1710 bp and the deduced amino acid was composed of a leader peptide, a variable domain, CH1, CH2, Hinge, CH3, CH4 and C-terminus, which was in accordance with most teleost. Absolute quantification PCR revealed that significant expression of Rag1 appeared earlier than Igμ , 61 and 95 dph compared to 95 dph, respectively. Here we report the first transcriptomic analysis of G. macrocephalus as the starting point for genetic research on immune system development towards improving the Pacific cod aquaculture. [ABSTRACT FROM AUTHOR]

Human bone marrow mesenchymal stem cells (hBM-MSCs) favor tumor growth and metastasis in vivo and in vitro. Neovascularization is involved in several pathological conditions, including tumor growth and metastasis. Previous studies have demonstrated that human bone marrow MSC-derived conditioned medium (hBM-MSC-CM) can promote tumor growth by inducing the expression of vascular epidermal growth factor (VEGF) in tumor cells. However, the effect of BM-MSCs on tumor lymph vessel formation has yet to be elucidated. In the present study, the effect of BM-MSCs on processes involved in lymph vessel formation, including tube formation, migration and proliferation, was investigated in human-derived lymphatic endothelial cells (HDLECs). It was identified that hBM-MSC-CM promoted the tube formation and migration of HDLECs. In addition, tumor cells were revealed to participate in lymph vessel formation. In the present study, the SGC-7901, HGC-27 and GFP-MCF-7 cell lines were treated with hBM-MSC-CM. The results demonstrated that the expression of the lymph-associated markers, prospero homeobox protein 1 and VEGF receptor-3, were increased in the SGC-7901 and HGC-27 cell lines, but not in the GFP-MCF-7 cells. The tube formation assay demonstrated that the HGC-27 cells treated with hBM-MSC-CM for 20 days underwent tube formation. These findings indicate that hBM-MSC-CM can promote tube formation in HDLECs and HGC-27 cells, which may be associated with lymph vessel formation during tumor growth and metastasis. [ABSTRACT FROM AUTHOR]

An immortalized mouse fetal liver stromal cell line, named KM3, has demonstrated the potential to support the growth and maintenance of human embryonic stem cells (hESCs). In this study, the characteristics of KM3 cells were examined following cryopreservation at -70°C and in liquid nitrogen for 15, 30 and 60 days following treatment with 10 µg/ml mitomycin C. In addition, whether the KM3 cells were suitable for use as feeder cells to support the growth of hESCs was evaluated. The inhibition of mitosis without cell death was observed when the KM3 cells were treated with 10 µg/ml mitomycin C for 2 h. The morphology of the KM3 cells cryopreserved in liquid nitrogen for 60 days was not markedly changed, and the cell survival rate was 84.60±1.14%. By contrast, the survival rate of the KM3 cells was 66.40±2.88% following cryopreservation at -70°C for 60 days; the cells readily detached, were maintained for a shorter time, and had a reduced expression level of basic fibroblast growth factor. hESCs cultured on KM3 cells cryopreserved in liquid nitrogen for 60 days showed the typical bird's nest structure, with clear boundaries and a differentiation rate of 16.33±2.08%. The differentiation rate of hESCs cultured on KM3 cells cryopreserved at -70°C for 60 days was 37.67±3.51%. These results indicate that the cryopreserved KM3 cells treated with mitomycin C may be directly used in the subculture of hESCs, and the effect is relatively good with -70°C short-term or liquid nitrogen cryopreservation. [ABSTRACT FROM AUTHOR]

Introduction: Administration of bone marrow mesenchymal stem cells (MSCs) or secreted microvesicles improves recovery from acute kidney injury (AKI). However, the potential roles and mechanisms are not well understood. In the current study, we focused on the protective effect of exosomes derived from human umbilical cord mesenchymal stem cells (hucMSC-ex) on cisplatin-induced nephrotoxicity in vivo and in vitro. Methods: We constructed cisplatin-induced AKI rat models. At 24 h after treatment with cisplatin, hucMSC-ex were injected into the kidneys via the renal capsule; human lung fibroblast (HFL-1)-secreted exosomes (HFL-1-ex) were used as controls. All animals were killed at day 5 after administration of cisplatin. Renal function, histological changes, tubular apoptosis and proliferation, and degree of oxidative stress were evaluated. In vitro, rat renal tubular epithelial (NRK-52E) cells were treated with or without cisplatin and after 6 h treated with or without exosomes. Cells continued to be cultured for 24 h, and were then harvested for western blotting, apoptosis and detection of degree of oxidative stress. Results: After administration of cisplatin, there was an increase in blood urea nitrogen (BUN) and creatinine (Cr) levels, apoptosis, necrosis of proximal kidney tubules and formation of abundant tubular protein casts and oxidative stress in rats. Cisplatin-induced AKI rats treated with hucMSC-ex, however, showed a significant reduction in all the above indexes. In vitro, treatment with cisplatin alone in NRK-52E cells resulted in an increase in the number of apoptotic cells, oxidative stress and activation of the p38 mitogen-activated protein kinase (p38MAPK) pathway followed by a rise in the expression of caspase 3, and a decrease in cell multiplication, while those results were reversed in the hucMSCs-ex-treated group. Furthermore, it was observed that hucMSC-ex promoted cell proliferation by activation of the extracellular-signal-regulated kinase (ERK)1/2 pathway. Conclusions: The results in the present study indicate that hucMSC-ex can repair cisplatin-induced AKI in rats and NRK-52E cell injury by ameliorating oxidative stress and cell apoptosis, promoting cell proliferation in vivo and in vitro. This suggests that hucMSC-ex could be exploited as a potential therapeutic tool in cisplatin-induced nephrotoxicity. [ABSTRACT FROM AUTHOR]

We use inelastic neutron scattering to study the effect of an in-plane magnetic field on the magnetic resonance in optimally doped superconductors FeSe0.4Te0.6 (Tc=14 K) and BaFe1.9Ni0.1As2 (Tc=20 K). While the magnetic field up to 14.5 T does not change the energy of the resonance, it partially suppresses Tc and the corresponding superconductivity-induced intensity gain of the mode. However, we find no direct evidence for the field-induced spin-1 Zeeman splitting of the resonance. Therefore it is still unclear if the resonance is the long-sought singlet-triplet excitation directly coupled to the superconducting electron Cooper pairs. [ABSTRACT FROM AUTHOR]

A combined study of mineral O and Rb–Sr isotopes was carried out for a number of Mesozoic granitoids in China in order to compare the degree of O isotope equilibrium between coexisting minerals, with the validity of mineral Rb–Sr isochrons for granitoids. A scrutiny of both O isotope geothermometry and Rb–Sr internal isochron dating for corresponding minerals indicates that equilibrium O isotope fractionation between Rb–Sr isochron minerals corresponds to geologically meaningful isochron ages if the variation in 87Rb/86Sr ratio is big enough to provide reasonably small uncertainties in age. Significant deviation of the Rb–Sr isochron age from the actual age appears to depend on the difference in Sr isotopic composition between an external fluid and the igneous minerals. As a result, O isotope disequilibrium is often caused by interaction between the rock and the external fluid that results in mineral alteration. Post-magmatic alteration can cause isotope exchange between the minerals and an internally buffered fluid that is isotopically identical to the host rock. The O isotope composition of coexisting minerals in studied samples changed principally due to a decrease in temperature. Both Rb and Sr concentrations and the Sr isotope ratios of isochron minerals also changed due to the mixing of different Sr reservoirs. Nevertheless, the isochron age can remain unchanged if the mixing took place along the isochron chord between the internal fluid and the minerals from that newly altered minerals formed. This provides an insight into the effect of internal and external fluids on the validity of mineral Rb–Sr chronometry. In addition, an alternative approach is proposed to construct the cooling curve by a combined use of O isotope temperature and mineral isotope age for the granitoids of interest. Comparing with the traditional method using the empirical closure temperature for Rb–Sr chronometry, the proposed approach utilizes fewer variables with smaller uncertainties than the traditional way. [ABSTRACT FROM AUTHOR]

Three new oleanane-skeleton triterpenoid saponins, 3β,4β,16α-17-carboxy-16,24-dihydroxy-28-norolean-12-en-3-yl 4-O-β-D-xylopyranosyl-β-D-glucopyranosiduronic acid (1), (3β,4β,16α)-17-carboxy-16,24-dihydroxy-28-norolean-12-en-3-yl β-D-glucopyranosiduronic acid methyl ester (2), and (3β,4β)-24-hydroxy-16-oxo-28-norolean-12-en-3-yl 4-O-β-D-xylopyranosyl-β-D-glucopyranosiduronic acid (3), together with eight known constituents, i.e., the oleanane-type triterpenoids 4–6, and the ursane-type triterpenoids 7–11, were isolated from the spikes of Prunella vulgaris. The new structures were established by means of detailed spectroscopic analysis (IR, HR-ESI-MS, 1D- and 2D-NMR experiments). Compounds 1–3 were tested for their inhibition activity against the growth of tumor cell lines; only compound 3 displayed marginal inhibition activity. [ABSTRACT FROM AUTHOR]

To investigate multitissue engraftment of human primitive hematopoietic cells and their differentiation in goats, human CD34+Lin- cord blood cells transduced with a GFP vector were transplanted into fetal goats at 45-55 days of gestation. GFP+ cells were detected in hematopoietic and nonhematopoietic organs including blood, bone marrow, spleen, liver, kidney, muscle, lung, and heart of the recipient goats (1.2-36% of all cells examined). We identified human β2 microglobulin-positive cells in multiple tissues. GFP+ cells sorted from the perfused liver of a transplant goat showed human insulin-like growth factor 1 gene sequences, indicating that the engrafted GFP+ cells were of human origin. A substantial fraction of cells engrafted in goat livers expressed the human hepatocyte-specific antigen, proliferating cell nuclear antigen, albumin, hepatocyte nuclear factor, and GFP. DNA content analysis showed no evidence for cellular fusion. Long-term engraftment of GFP+ cells could be detected in the blood of goats for up to 2 yr. Microarray analysis indicated that human genes from a variety of functional categories were expressed in chimeric livers and blood. The human/goat xenotransplant model provides a unique system to study the kinetics of hematopoietic stem cell engraftment, gene expression, and possible stem cell plasticity under noninjured conditions. [ABSTRACT FROM AUTHOR]

We have injected human CD34+lin- cells derived from cord blood (CB) into the goat fetuses via in utero at 45–55 days gestation under guidance of B-scan ultrasonograph. Sixty out of 68 fetuses injected survived to full term. The long-term survival of the human cells in transplant goat has been tested by various experimental methods, including FACS analysis, real-time PCR, RT-PCR, Southern-blot hybridization, FISH, as well as immunohistochemical assays. All the 60 transplant goats demonstrated engrafted human cells, including myeloid, B-lymphoid, and erythroid lineages. The yield of the human CD34+ cells varied, but was not linked with sex and age. High numbers of human cells could be detected for at least 16 months after birth. Immunohistochemical analyses revealed that the human cells were present not only in blood but also in other tissues, such as liver, of the transplant goats. In addition, a human-specific serum albumin and the hepatocyte nuclear factor (hHNF-3β) mRNAs specific to human hepato-antigen could be readily detected in the livers of the transplant goats. Our results demonstrate that this in utero xenograft model should be useful for expansion of human HSC and possibly for the evaluating the effectiveness of prenatal treatment of human genetic diseases. [ABSTRACT FROM AUTHOR]

New wide-angle reflection and refraction seismic data provide constraints on the structure of the upper lithosphere, and test models of its evolution to raise the northeastern part of the Tibetan Plateau. Amplitudes observed for reflections from the crust–mantle boundary are sufficiently large to suggest that there is no significant partial melt in the deep crust. The data show an increase of the crustal thickness between terranes from north of the Kun Lun Fault into the Qang Tang of central Tibet, and a contrast among their intracrustal images and compositions. In the north, P and S velocities are consistent with a dominantly felsic composition and show that only the upper crust thickened. South of the Kun Lun Fault a thicker crust made of two layers could result from the superposition of the originally thin crust of the Bayan Har terrane on the lower part of the crust of the domain to the north, which upper crust it shoved and thickened. Different modes of crustal thickening, either by thickening of individual layers or superpositions and imbrication among them appear to work jointly to raise the topography. [Copyright &y& Elsevier]

In the mononuclear title complex, [Pd(C17H12N2S2)Cl2], the 8-(2-benzo­thia­zolyl­sulfanyl­meth­yl)­quinoline ligand chelates to PdCl2 through its N atoms, conferring a square planar geometry on Pd. The angles around the Pd atom range from 88.04 (6) to 92.76 (3)°. [ABSTRACT FROM AUTHOR]

Atomic force microscopy experiments found that GB1, a typical two-state model protein used for study of folding and unfolding dynamics, can sustain forces of more than 100 pN, but its response to low forces still remains unclear. Using ultrastable magnetic tweezers, we discovered that GB1 has an unexpected nonmonotonic force-dependent unfolding rate at 5-160 pN, from which a free energy landscape with two main barriers and a hidden intermediate state was constructed. A model combining two separate models by Dudko et al. with two pathways between the native state and this intermediate state is proposed to rebuild the unfolding dynamics over the full experimental force range. One candidate of this transient intermediate state is the theoretically proposed molten globule state with a loosely collapsed conformation, which might exist universally in the folding and unfolding processes of two-state proteins. [ABSTRACT FROM AUTHOR]