Neutron Polarization Analysis for Biphasic Solvent Extraction Systems

We performed neutron polarization analysis (NPA) of extracted organic phases containing complexes, comprised of Zr(NO₃)₄ and tri-n-butyl phosphate, which enabled decomposition of the intensity distribution of small-angle neutron scattering (SANS) into the coherent and incoherent scattering components. The coherent scattering intensity, containing structural information, and the incoherent scattering compete over a wide range of magnitude of scattering vector, q, specifically when q is larger than q* ≈ 1/R_g, where R_g is the radius of gyration of scatterer. Therefore, it is important to determine the incoherent scattering intensity exactly to perform an accurate structural analysis from SANS data when R_g is small, such as the aforementioned extracted coordination species. Although NPA is the best method for evaluating the incoherent scattering component for accurately determining the coherent scattering in SANS, this method is not used frequently in SANS data analysis because it is technically challenging. In this study, we successfully demonstrated that experimental determination of the incoherent scattering using NPA is suitable for sample systems containing a small scatterer with a weak coherent scattering intensity, such as extracted complexes in biphasic solvent extraction systems.     

Importance of dispersibility of TiO2 in preparation of TiO2-dispersed microspheres by Shirasu porous glass (SPG) membrane emulsification

The preparation of the highly refractive transparent TiO₂-dispersed microspheres with uniform size was studied. These nanocomposite microspheres were prepared via TiO₂ dispersion in an acrylic monomer and the emulsification by the Shirasu porous glass (SPG) membrane technique. Two kinds of the dispersion methods (bead mill dispersion with fine beads and ultrasonic dispersion) were carried out. The suspension prepared by bead mill included well-dispersed TiO₂ nanoparticles and led to the uniformly sized TiO₂-dispersed microspheres. It was indicated that the dispersibility of TiO₂ in a monomer was the important factor in this process.     

A newly identified horseshoe crab lectin with specificity for blood group A antigen recognizes specific O-antigens of bacterial lipopolysaccharides

A 14-kDa lectin, named tachylectin-3, was newly identified from hemocytes of the Japanese horseshoe crab, Tachypleus tridentatus. This lectin exhibited hemagglutinating activity against human A-type erythrocytes, but not against the B- and O-types of erythrocytes and animal erythrocytes, including those of sheep, rabbit, horse, and bovine. The hemagglutinating activity of tachylectin-3 was equivalent to that of a previously identified lectin, named tachylectin-2, with affinity for N-acetyl-D-glucosamine or N-acetyl-D-galactosamine. However, the activity of tachylectin-3 was not inhibited by these two N-acetylhexosamines at 100 mM but was inhibited by a blood group A-pentasaccharide at a minimum inhibitory concentration of 0.16 mM. Furthermore, the hemagglutinating activity was strongly inhibited by bacterial S-type lipopolysaccharides (LPSs) from Gram-negative bacteria but not by R-type LPSs lacking O-antigens. One of the most effective S-type LPSs was from Escherichia coli O111:B4, with a minimum inhibitory concentration of 6 ng/ml. These data suggest that tachylectin-3 specifically recognizes Gram-negative bacteria through the unique structural units of O-antigens. Ultracentrifugation analysis revealed that tachylectin-3 is present in dimer in solution. A cDNA coding for tachylectin-3 was isolated from a hemocyte cDNA library. Tachylectin-3 consisted of two repeating sequences, each with a partial sequence similarity to rinderpest virus neuraminidase. Tachylectin-3 and three previously isolated types of tachylectins were all predominantly expressed in hemocytes and released from hemocytes in response to external stimuli. These lectins present at injured sites suggest that they probably serve synergistically to accomplish an effective host defense against invading microbes.     

Evolving neural controllers that elicit nontrivial behaviors using a developmental process

Recently, evolutionary robotics (ER) has been attracting a lot of attention in the field of robotics artificial life and so on. ER approaches are expected to provide feasible methods to design controllers for autonomous mobile robots with less human intervention. However, most of the conventional studies in ER have been aiming at obtaining very simple (trivial) behaviors such as obstacle avoiding, wall following, and target approaching. To make the ER approach more fruitful, we should pay close attention to obtaining nontrivial behaviors. Based on these considerations, in this paper we propose a method for obtaining nontrivial behaviors using a developmental process with a carefully arranged grafting method. To verify the validity, we apply our idea to the construction of neural controllers that can cope with rough terrain. This work was presented, in part, at the Third International Symptosium on Artificial Life and Robotics, Oita, Japan, January 19–21, 1998     

Potential health benefits of conjugated trienoic acids

Current studies on physiological functions of certain plant seed oils containing conjugated trienoic acids as a major fatty acid component are indicative of the possible usefulness of these oils as a new type of functional oils. Here, we describe the potential health benefits of conjugated trienoic acids.     

Measurements of activation cross sections of (n,p) and (n, α) reactions in the energy range of 3.5–5.9 MeV using a deuterium gas target

Activation cross sections of (n, p) and (n, α) reactions were measured by means of the activation method in the neutron energy range of 3.5–5.9 MeV using a deuterium gas target. The irradiated target isotopes were ²⁷Al, ^28,29Si, ⁴¹K, ⁵¹V, ⁶¹Ni, ⁶⁵Cu, ^64,67Zn, ⁶⁹Ga, ⁷⁹Br, ⁹²Mo and ⁹³Nb. The cross sections of the ²⁹Si(n, p) ²⁹Al, ⁶⁷Zn(n, p) ⁶⁷Cu, ⁶⁹Ga(n, p) ^69mZn, ⁷⁹Br(n, p) ^79mSe, and ⁶⁹Ga(n, α) ⁶⁶Cu reactions were obtained for the first time in the studied energy range. The d-D neutrons were generated by the deuterium gas target at the Van de Graaff accelerator (KN-VdG) at Nagoya University. All cross section values were determined relative to those of the ¹¹⁵In(n, n′)^115mIn reaction. The activities induced by the low-energy neutrons were corrected. For the corrections, the neutron spectra and mean neutron energies at the irradiation positions were calculated taking into account the energy loss of incident deuterons, the angular differential cross section of the d-D reaction and the solid angle subtended by the sample. The systematics of the (n, p) reactions at the neutron energy of 5.0 MeV in the mass range between 27 and 92 were proposed for the first time. This systematics can predict the cross sections within an accuracy of a factor of 1.6.     

Tomographic reconstruction technique for pulsed-echo imaging

This article proposes a tomographic reconstruction technique using divergent ultrasonic waves of a circular arc wavefront which are formed by one-dimensional thin-phased array. The projection data which are obtained by phasing of transmitting and receiving signals are applied to the filtered back projection algorithm so that the image at the spherical surface is reconstructed. The experiments using a small steel sphere and a layer phantom of agar gel are performed using a commercially available phased-array system. The divergent waves are formed by the slit in the front of the array. As a result, images with a space-invariant, high-resolution unlike conventional B-scan image are obtained. © 1997 John Wiley & Sons, Inc. Int J Imaging Syst Technol, 8, 432–437, 1997     

Diclofenac-Induced Cytotoxicity in Direct and Indirect Co-Culture of HepG2 Cells with Differentiated THP-1 Cells

Non-steroidal anti-inflammatory drugs (NSAIDs) such as diclofenac (DIC) frequently induce drug-induced liver injury (DILI). It is unclear whether macrophages such as M1 and M2 participate in NSAID-associated DILI; elucidating this relationship could lead to a better understanding of the detailed mechanism of DILI. We co-cultured human hepatoma HepG2 cells with M1 or M2 derived from human monocytic leukemia THP-1 cells to examine the roles of M1 and M2 in DIC-induced cytotoxicity. DIC was added to the direct or indirect co-cultures of HepG2 cells with M1 or M2 (HepG2/M1 or HepG2/M2, respectively) at cell ratios of (1:0, 1:0.1, 1:0.4, and 1:1). In both direct and indirect HepG2/M2 co-cultures (1:0.4), there was lower lactate dehydrogenase release compared with HepG2/M1 co-cultures. Other NSAIDs as well as DIC showed similar protective effects of DIC-induced cytotoxicity. There were only slight differences in mRNA levels of apoptosis- and endoplasmic reticulum stress-associated factors between M1 and M2 after DIC treatment, suggesting that other factors determined the protective effects of M2 on DIC-induced cytotoxicity. Levels of high mobility group box 1 (HMGB1) in the medium and the mRNA expression levels of HMGB1 receptors were different between M1 and M2 after DIC treatment. Increased HMGB1 concentrations and expression of toll-like receptor 2 mRNA in M1 were observed compared with M2 after DIC treatment. In conclusion, these results suggested that the HMGB1/TLR2 signaling axis can be suppressed in M2 but not M1, leading to the different roles of M1 and M2 in NSAID-induced cytotoxicity.     

Chemical Synthesis of Side-Chain-Hydroxylated Vitamin D3 Derivatives and Their Metabolism by CYP27B1

1α,25-Dihydroxyvitamin D₃ (abbreviated here as 1,25D₃) is a hormonally active form of vitamin D₃ (D₃), and is produced from D₃ by CYP27 A1-mediated hydroxylation at C25, followed by CYP27B1-mediated hydroxylation at C1. Further hydroxylation of 25D₃ and 1,25D₃ occurs at C23, C24 and C26 to generate corresponding metabolites, except for 1,25R,26D₃. Since the capability of CYP27B1 to hydroxylate C1 of side-chain-hydroxylated metabolites other than 23S,25D₃ and 24R,25D₃ has not been examined, we have here explored the role of CYP27B1 in the C1 hydroxylation of a series of side-chain-hydroxylated D₃ derivatives. We found that CYP27B1 hydroxylates the R diastereomers of 24,25D₃ and 25,26D₃ more effectively than the S diastereomers, but shows almost no activity towards either diastereomer of 23,25D₃. This is the first report to show that CYP27B1 metabolizes 25,26D₃ to the corresponding 1α-hydroxylated derivative, 1,25,26D₃. It will be interesting to examine the physiological relevance of this finding.     

Targeting Epigenetic Regulators for Endometrial Cancer Therapy: Its Molecular Biology and Potential Clinical Applications

Endometrial cancer is one of the most frequently diagnosed gynecological malignancies worldwide. However, its prognosis in advanced stages is poor, and there are only few available treatment options when it recurs. Epigenetic changes in gene function, such as DNA methylation, histone modification, and non-coding RNA, have been studied for the last two decades. Epigenetic dysregulation is often reported in the development and progression of various cancers. Recently, epigenetic changes in endometrial cancer have also been discussed. In this review, we give the main points of the role of DNA methylation and histone modification in endometrial cancer, the diagnostic tools to determine these modifications, and inhibitors targeting epigenetic regulators that are currently in preclinical studies and clinical trials.