49 research outputs found
Imaging molecular orbitals with laser-induced electron tunneling spectroscopy
Photoelectron spectroscopy in intense laser fields has proven to be a
powerful tool for providing detailed insights into molecular structure. The
ionizing molecular orbital, however, has not been reconstructed from the
photoelectron spectra, mainly due to the fact that its phase information can be
hardly extracted. In this work, we propose a method to retrieve the phase
information of the ionizing molecular orbital with laser-induced electron
tunneling spectroscopy. By analyzing the interference pattern in the
photoelectron spectrum, the weighted coefficients and the relative phases of
the constituent atomic orbitals for a molecular orbital can be extracted. With
this information we reconstruct the highest occupied molecular orbital of
N. Our work provides a reliable and general approach for imaging of
molecular orbitals with the photoelectron spectroscopy.Comment: 6 pages, 4 figures, including Supplementary Material
Connectivity strength-weighted sparse group representation-based brain network construction for MCI classification: Weighted Sparse Group Model for MCI Classification
Brain functional network analysis has shown great potential in understanding brain functions and also in identifying biomarkers for brain diseases, such as Alzheimer's disease (AD) and its early stage, mild cognitive impairment (MCI). In these applications, accurate construction of biologically meaningful brain network is critical. Sparse learning has been widely used for brain network construction; however, its l1-norm penalty simply penalizes each edge of a brain network equally, without considering the original connectivity strength which is one of the most important inherent linkwise characters. Besides, based on the similarity of the linkwise connectivity, brain network shows prominent group structure (i.e., a set of edges sharing similar attributes). In this article, we propose a novel brain functional network modeling framework with a “connectivity strength-weighted sparse group constraint.” In particular, the network modeling can be optimized by considering both raw connectivity strength and its group structure, without losing the merit of sparsity. Our proposed method is applied to MCI classification, a challenging task for early AD diagnosis. Experimental results based on the resting-state functional MRI, from 50 MCI patients and 49 healthy controls, show that our proposed method is more effective (i.e., achieving a significantly higher classification accuracy, 84.8%) than other competing methods (e.g., sparse representation, accuracy = 65.6%). Post hoc inspection of the informative features further shows more biologically meaningful brain functional connectivities obtained by our proposed method
Learning-based 3T brain MRI segmentation with guidance from 7T MRI labeling: Learning-based 3T brain MRI segmentation
Segmentation of brain magnetic resonance (MR) images into white matter (WM), gray matter (GM), and cerebrospinal fluid (CSF) is crucial for brain structural measurement and disease diagnosis. Learning-based segmentation methods depend largely on the availability of good training ground truth. However, the commonly used 3T MR images are of insufficient image quality and often exhibit poor intensity contrast between WM, GM, and CSF. Therefore, they are not ideal for providing good ground truth label data for training learning-based methods. Recent advances in ultrahigh field 7T imaging make it possible to acquire images with excellent intensity contrast and signal-to-noise ratio
Bioactive Constituents of Verbena officinalis Alleviate Inflammation and Enhance Killing Efficiency of Natural Killer Cells
Natural killer (NK) cells play key roles in eliminating pathogen-infected cells. Verbena
officinalis (V. officinalis) has been used as a medical plant in traditional and modern medicine for
its anti-tumor and anti-inflammatory activities, but its effects on immune responses remain largely
elusive. This study aimed to investigate the potential of V. officinalis extract (VO extract) to regulate
inflammation and NK cell functions. We examined the effects of VO extract on lung injury in a mouse
model of influenza virus infection. We also investigated the impact of five bioactive components of
VO extract on NK killing functions using primary human NK cells. Our results showed that oral
administration of VO extract reduced lung injury, promoted the maturation and activation of NK
cells in the lung, and decreased the levels of inflammatory cytokines (IL-6, TNF-α and IL-1β) in the
serum. Among five bioactive components of VO extract, Verbenalin significantly enhanced NK killing
efficiency in vitro, as determined by real-time killing assays based on plate-reader or high-content
live-cell imaging in 3D using primary human NK cells. Further investigation showed that treatment
of Verbenalin accelerated the killing process by reducing the contact time of NK cells with their
target cells without affecting NK cell proliferation, expression of cytotoxic proteins, or lytic granule
degranulation. Together, our findings suggest that VO extract has a satisfactory anti-inflammatory
effect against viral infection in vivo, and regulates the activation, maturation, and killing functions of
NK cells. Verbenalin from V. officinalis enhances NK killing efficiency, suggesting its potential as a
promising therapeutic to fight viral infection
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Expression of the receptor tyrosine kinase ephb2 on dendritic cells is modulated by toll-like receptor ligation but is not required for t cell activation
The Eph receptor tyrosine kinases interact with their ephrin ligands on adjacent cells to facilitate contact-dependent cell communication. Ephrin B ligands are expressed on T cells and have been suggested to act as co-stimulatory molecules during T cell activation. There are no detailed reports of the expression and modulation of EphB receptors on dendritic cells, the main antigen presenting cells that interact with T cells. Here we show that mouse splenic dendritic cells (DC) and bone-marrow derived DCs (BMDC) express EphB2, a member of the EphB family. EphB2 expression is modulated by ligation of TLR4 and TLR9 and also by interaction with ephrin B ligands. Co-localization of EphB2 with MHC-II is also consistent with a potential role in T cell activation. However, BMDCs derived from EphB2 deficient mice were able to present antigen in the context of MHC-II and produce T cell activating cytokines to the same extent as intact DCs. Collectively our data suggest that EphB2 may contribute to DC responses, but that EphB2 is not required for T cell activation. This result may have arisen because DCs express other members of the EphB receptor family, EphB3, EphB4 and EphB6, all of which can interact with ephrin B ligands, or because EphB2 may be playing a role in another aspect of DC biology such as migration
Effects of Chitin and Its Derivative Chitosan on Postharvest Decay of Fruits: A Review
Considerable economic losses to harvested fruits are caused by postharvest fungal decay during transportation and storage, which can be significantly controlled by synthetic fungicides. However, considering public concern over pesticide residues in food and the environment, there is a need for safer alternatives for the control of postharvest decay to substitute synthetic fungicides. As the second most abundant biopolymer renewable source in nature, chitin and its derivative chitosan are widely used in controlling postharvest decay of fruits. This review aims to introduce the effect of chitin and chitosan on postharvest decay in fruits and the possible modes of action involved. We found most of the actions discussed in these researches rest on physiological mechanisms. All of the mechanisms are summarized to lay the groundwork for further studies which should focus on the molecular mechanisms of chitin and chitosan in controlling postharvest decay of fruits
Thyroid Disruption by Di-n-Butyl Phthalate (DBP) and Mono-n-Butyl Phthalate (MBP) in Xenopus laevis
BACKGROUND: Di-n-butyl phthalate (DBP), a chemical widely used in many consumer products, is estrogenic and capable of producing seriously reproductive and developmental effects in laboratory animals. However, recent in vitro studies have shown that DBP and mono-n-butyl phthalate (MBP), the major metabolite of DBP, possessed thyroid hormone receptor (TR) antagonist activity. It is therefore important to consider DBP and MBP that may interfere with thyroid hormone system. METHODOLOGY/PRINCIPAL FINDINGS: Nieuwkoop and Faber stage 51 Xenopus laevis were exposed to DBP and MBP (2, 10 or 15 mg/L) separately for 21 days. The two test chemicals decelerated spontaneous metamorphosis in X. laevis at concentrations of 10 and 15 mg/L. Moreover, MBP seemed to possess stronger activity. The effects of DBP and MBP on inducing changes of expression of selected thyroid hormone response genes: thyroid hormone receptor-beta (TRβ), retinoid X receptor gamma (RXRγ), alpha and beta subunits of thyroid-stimulating hormone (TSHα and TSHβ) were detected by qPCR at all concentrations of the compounds. Using mammalian two-hybrid assay in vitro, we found that DBP and MBP enhanced the interactions between co-repressor SMRT (silencing mediator for retinoid and thyroid hormone receptors) and TR in a dose-dependent manner, and MBP displayed more markedly. In addition, MBP at low concentrations (2 and 10 mg/L) caused aberrant methylation of TRβ in head tissue. CONCLUSIONS: The current findings highlight potential disruption of thyroid signalling by DBP and MBP and provide data for human risk assessment
Black phosphorus@Au NPs decorated on a porous spherical montmorillonite as a self-sedimentary catalyst for cost-effective and efficient catalysis
Black phosphorus (BP) has exhibited its potential application as the cocatalyst substrate for catalytic reduction of organic pollutants due to its excellent electron transfer ability. However, the application was limited by the reuse process due to its light mass with abundant recovery devices involved. In this work, a micro-sized spherical montmorillonite (SMt) with the self-sedimentary property was used to support BP@Au NPs. The strong adsorption ability of porous SMt could increase the concentration of 4-nitrophenol near the catalytic active sites, thus, accelerating the catalytic process. The optimized apparent reduction rate constant of 6.1 min-1 and the turnover frequency of 648 h-1 were obtained, which was one of the most efficient catalytic system. More importantly, the fabricated SMt supported heterogeneous catalyst could be facile recycled without any devices involved. The morphology and catalytic performance were almost unaltered after recycling 20 times. Our straightforward strategy to solve the issue of the reuse process through a self-sedimentary substrate facilitates the practical application of these catalysts in the reduction of organic pollutants