3,857 research outputs found
Finger-gate manipulated quantum transport in a semiconductor narrow constriction with spin-orbit interactions and Zeeman effect
The authors investigate quantum transport in a narrow constriction fabricated
by narrow band gap semiconductor materials with spin-orbit (SO) couplings. We
consider the Rashba-Dresselhaus (RD) spin-orbit interactions (SOIs) and the
Zeeman effect induced by an in-plane magnetic field along the transport
direction. The interplay of the RD-SOI and the Zeeman effect may induce a
SOI-Zeeman gap and influence the transport properties. We demonstrate that an
attractive scattering potential may induce electron-like quasi-bound-state
feature and manifest the RD-SOI-Zeeman induced Fano line-shape in conductance.
Furthermore, a repulsive scattering potential may induce hole-like
quasi-bound-state feature on the subband top of the lower spin branch.Comment: 10 pages, 9 figure
Lutein Protects against Methotrexate-Induced and Reactive Oxygen Species-Mediated Apoptotic Cell Injury of IEC-6 Cells
Purpose High-dose chemotherapy using methotrexate (MTX) frequently induces side effects such as mucositis that leads to intestinal damage and diarrhea. Several natural compounds have been demonstrated of their effectiveness in protecting intestinal epithelial cells from these adverse effects. In this paper, we investigated the protection mechanism of lutein against MTX-induced damage in IEC-6 cells originating from the rat jejunum crypt. Methods: The cell viability, induced-apoptosis, reactive oxygen species (ROS) generation, and mitochondrial membrane potential in IEC-6 cells under MTX treatment were examined in the presence or absence of lutein. Expression level of Bcl2, Bad and ROS scavenging enzymes (including SOD, catalase and Prdx1) were detected by quantitative RT-PCR. Results: The cell viability of IEC-6 cells exposed to MTX was decreased in a dose- and time-dependent manner. MTX induces mitochondrial membrane potential loss, ROS generation and caspase 3 activation in IEC-6 cells. The cytotoxicity of MTX was reduced in IEC-6 cells by the 24 h pre-treatment of lutein. We found that pre-treatment of lutein significantly reduces MTX-induced ROS and apoptosis. The expression of SOD was up-regulated by the pre-treatment of lutein in the MTX-treated IEC-6 cells. These results indicated that lutein can protect IEC-6 cells from the chemo-drugs induced damage through increasing ROS scavenging ability. Conclusion: The MTX-induced apoptosis of IEC-6 cells was shown to be repressed by the pre-treatment of lutein, which may represent a promising adjunct to conventional chemotherapy for preventing intestinal damages
FFTPL: An Analytic Placement Algorithm Using Fast Fourier Transform for Density Equalization
We propose a flat nonlinear placement algorithm FFTPL using fast Fourier
transform for density equalization. The placement instance is modeled as an
electrostatic system with the analogy of density cost to the potential energy.
A well-defined Poisson's equation is proposed for gradient and cost
computation. Our placer outperforms state-of-the-art placers with better
solution quality and efficiency
Fucosyltransferase 1 and 2 play pivotal roles in breast cancer cells.
FUT1 and FUT2 encode alpha 1, 2-fucosyltransferases which catalyze the addition of alpha 1, 2-linked fucose to glycans. Glycan products of FUT1 and FUT2, such as Globo H and Lewis Y, are highly expressed on malignant tissues, including breast cancer. Herein, we investigated the roles of FUT1 and FUT2 in breast cancer. Silencing of FUT1 or FUT2 by shRNAs inhibited cell proliferation in vitro and tumorigenicity in mice. This was associated with diminished properties of cancer stem cell (CSC), including mammosphere formation and CSC marker both in vitro and in xenografts. Silencing of FUT2, but not FUT1, significantly changed the cuboidal morphology to dense clusters of small and round cells with reduced adhesion to polystyrene and extracellular matrix, including laminin, fibronectin and collagen. Silencing of FUT1 or FUT2 suppressed cell migration in wound healing assay, whereas FUT1 and FUT2 overexpression increased cell migration and invasion in vitro and metastasis of breast cancer in vivo. A decrease in mesenchymal like markers such as fibronectin, vimentin, and twist, along with increased epithelial like marker, E-cadherin, was observed upon FUT1/2 knockdown, while the opposite was noted by overexpression of FUT1 or FUT2. As expected, FUT1 or FUT2 knockdown reduced Globo H, whereas FUT1 or FUT2 overexpression showed contrary effects. Exogenous addition of Globo H-ceramide reversed the suppression of cell migration by FUT1 knockdown but not the inhibition of cell adhesion by FUT2 silencing, suggesting that at least part of the effects of FUT1/2 knockdown were mediated by Globo H. Our results imply that FUT1 and FUT2 play important roles in regulating growth, adhesion, migration and CSC properties of breast cancer, and may serve as therapeutic targets for breast cancer
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A Methodology for Evaluating Data and Output Misfits in Commercial Off-The-Shelf ERP Systems
This paper presents a methodology based on the task-technology fit theory to identify data and output misfits in the ex-ante evaluation of an off-the shelf enterprise resources planning (ERP) package. The proposed methodology consists of two stages: output misfit analysis and data misfit analysis. The purpose of the first stage is to identify corresponding field (output misfits) and data glossary for data misfit analysis. The latter stage identifies data misfits for every corresponding activity in the business process sequence. The proposed methodology provides a systematic approach to alleviate the difficulty and complexity in identifying data and output misfits. The identification results identify where the misfits are and provide a degree of mismatch, thus providing a practical basis for ERP tool selection to reduce the risk of failure in its implementation
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α-Lactosylceramide Protects Against iNKT-Mediated Murine Airway Hyperreactivity and Liver Injury Through Competitive Inhibition of Cd1d Binding.
Invariant natural killer T (iNKT) cells, which are activated by T cell receptor (TCR)-dependent recognition of lipid-based antigens presented by the CD1d molecule, have been shown to participate in the pathogenesis of many diseases, including asthma and liver injury. Previous studies have shown the inhibition of iNKT cell activation using lipid antagonists can attenuate iNKT cell-induced disease pathogenesis. Hence, the development of iNKT cell-targeted glycolipids can facilitate the discovery of new therapeutics. In this study, we synthesized and evaluated α-lactosylceramide (α-LacCer), an α-galactosylceramide (α-GalCer) analog with lactose substitution for the galactose head and a shortened acyl chain in the ceramide tail, toward iNKT cell activation. We demonstrated that α-LacCer was a weak inducer for both mouse and human iNKT cell activation and cytokine production, and the iNKT induction by α-LacCer was CD1d-dependent. However, when co-administered with α-GalCer, α-LacCer inhibited α-GalCer-induced IL-4 and IFN-γ production from iNKT cells. Consequently, α-LacCer also ameliorated both α-GalCer and GSL-1-induced airway hyperreactivity and α-GalCer-induced neutrophilia when co-administered in vivo. Furthermore, we were able to inhibit the increases of ConA-induced AST, ALT and IFN-γ serum levels through α-LacCer pre-treatment, suggesting α-LacCer could protect against ConA-induced liver injury. Mechanistically, we discerned that α-LacCer suppressed α-GalCer-stimulated cytokine production through competing for CD1d binding. Since iNKT cells play a critical role in the development of AHR and liver injury, the inhibition of iNKT cell activation by α-LacCer present a possible new approach in treating iNKT cell-mediated diseases
Application of the SUSTAIN Model to a Watershed-Scale Case for Water Quality Management
[[abstract]]Low impact development (LID) is a relatively new concept in land use management that aims to maintain hydrological conditions at a predevelopment level without deteriorating water quality during land development. The United States Environmental Protection Agency (USEPA) developed the System for Urban Stormwater Treatment and Analysis Integration model (SUSTAIN) to evaluate the performance of LID practices at different spatial scales; however, the application of this model has been limited relative to LID modeling. In this study, the SUSTAIN model was applied to a Taiwanese watershed. Model calibration and verification were performed, and different types of LID facilities were evaluated. The model simulation process and the verified model parameters could be used in other cases. Four LID scenarios combining bioretention ponds, grass swales, and pervious pavements were designed based on the land characteristics. For the SUSTAIN model simulation, the results showed that pollution reduction was mainly due to water quantity reduction, infiltration was the dominant mechanism and plant interception had a minor effect on the treatment. The simulation results were used to rank the primary areas for nonpoint source pollution and identify effective LID practices. In addition to the case study, a sensitivity analysis of the model parameters was performed, showing that the soil infiltration rate was the most sensitive parameter affecting the LID performance. The objectives of the study are to confirm the applicability of the SUSTAIN model and to assess the effectiveness of LID practices in the studied watershed.[[notice]]補正完畢[[incitationindex]]SCI[[booktype]]電子
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