Extreme structure and spontaneous lift of spin degeneracy in doped perforated bilayer graphenes

Extreme structure and spin states of doped and undoped perforated bigraphenes was studied using DFT simulations. It was found that folded nanopores possess extremely high curvature of 0.34 Å−1. Dramatic structural deformation causes severe changes of the chemical properties of carbon atoms localized at the nanopores converting the folded edges to local oxidative fragments. It was found that asymmetrical coordination of either Li, Ca, or Al to the nanopores is coupled with electron transfer from metal to edge carbon atoms and breakdown of local inversion symmetry. Li-, Ca-, and Al-doped perforated AA bigraphene revealed ferromagnetic spin ordering with magnetic moments of 0.38, 0.14, and 0.32μB/unit cell, respectively, and spin polarization energy gain of 0.037eV for Ca-doped superlattice. It was shown that ferromagnetic spin ordering of bigraphene nanopores contradicts to the Nagaoka's theorem, which excludes strong electron correlations as a reason of spin polarization. Spontaneous lift of spin degeneracy was interpreted in terms of perturbing intense local electrostatic fields from extra electron charges localized at the nanopore edges, coupled with breakdown of space inversion and local translation invariances. It was shown that spin energy splitting is proportional to the matrix elements calculated on Bloch states with opposite wavevectors and perturbing electrostatic fields

Identification and characterization of mesenchymal-epithelial progenitor-like cells in normal and injured rat liver

In normal rat liver, thymocyte antigen 1 (Thy1) is expressed in fibroblasts/myofibroblasts and in some blood progenitor cells. Thy1-expressing cells also accumulate in the liver during impaired liver regeneration. The origin and nature of these cells are not well understood. By using RT-PCR analysis and immunofluorescence microscopy, we describe the presence of rare Thy1(+) cells in the liver lobule of normal animals, occasionally forming small collections of up to 20 cells. These cells constitute a small portion (1.7% to 1.8%) of nonparenchymal cells and reveal a mixed mesenchymal-epithelial phenotype, expressing E-cadherin, cytokeratin 18, and desmin. The most potent mitogens for mesenchymal-epithelial Thy1(+) cells in vitro are the inflammatory cytokines interferon γ, IL-1, and platelet-derived growth factor-BB, which are not produced by Thy1(+) cells. Thy1(+) cells express all typical mesenchymal stem cell and hepatic progenitor cell markers and produce growth factor and cytokine mRNA (Hgf, Il6, Tgfa, and Tweak) for proteins that maintain oval cell growth and differentiation. Under appropriate conditions, mesenchymal-epithelial cells differentiate in vitro into hepatocyte-like cells. In this study, we show that the adult rat liver harbors a small pool of endogenous mesenchymal-epithelial cells not recognized previously. In the quiescent state, these cells express both mesenchymal and epithelial cell markers. They behave like hepatic stem cells/progenitors with dual phenotype, exhibiting high plasticity and long-lasting proliferative activity

Fluorescence investigations of phototransformation of phenol in aqueous solutions

Оцифровано в НБ ТГ

Fluorescence investigations of phototransformation of phenol in aqueous solutions

Оцифровано в НБ ТГ

Control System of Parameters of the Azimuthal Module

Analytical and experimental studies of the azimuthal module of two-component vibrational micromechanical gyroscope were conducted. It is shown that the micromechanical gyroscope is a system with distributed parameters. The frequency analysis is performed using software T-Flex. The influence of mechanical disturbances on the movement of azimuthal module in the form of translational and angular oscillations is shown; the natural frequencies of the azimuth are defined

Age-Dependent Changes in Glutathione-S-Transferase: Correlation with Total Plasma Antioxidant Potential and Red Cell Intracellular Glutathione

The correlation between antioxidant capacity and oxidative damage during aging has been reported in several tissues in different species. Glutathione-S-transferases (GST) can metabolise endogenous and exogenous toxins and carcinogens by catalysing the conjugation of diverse electrophiles with reduced glutathione (GSH). We observe a significant (P < 0.001) increase in plasma GST activity as a function of human age (r = 0.5675). A significant (P < 0.001) positive correlation (r = 0.8979) is observed between GST activity and total plasma antioxidant potential measured as ferric reducing ability of the plasma (FRAP). GST activity and red cell intracellular GSH also show a significant positive correlation (r = 0.7014). We hypothesize that the increased activity of plasma GST is a manifestation of increased generation of ROS and a concomitant decrease in the level of plasma antioxidant capacity during aging