Sulfated sialyl Lewis X, the putative L-selectin ligand, detected on endothelial cells of high endothelial venules by a distinct set of anti-sialyl Lewis X antibodies

Endothelial cells of high endothelial venules (HEV) in human peripheral lymph nodes expressed a distinct type of sialyl Lewis X antigen, which was detected preferentially with a set of anti-sialyl Lewis X antibodies, 2F3, 2H5 and HECA-452 in immunohistochemistry, while another set of anti-sialyl Lewis X antibodies, FH-6 and CSLEX-1, failed to detect it. The adhesion of cells expressing L-selectin to HEV was inhibited by members of the former set of antibodies in Stamper-Woodruff assays performed on frozen sections of human peripheral lymph nodes. Transfection of a cultured endothelial cell line with a human alpha1-->3 fucosyltransferase, Fuc-T VII, resulted in the expression of a distinct type of sialyl Lewis X antigen having the reactivity similar to that of HEV; i.e., the antigen appearing on the transfectant clone was detectable only with the set of 2F3, 2H5 and HECA-452, but not with the set of FH-6 and CSLEX-1. Treatment of transfectant cells with sodium chlorate, a metabolic inhibitor of sulfation, resulted in reactivity to the members of the latter set of antibodies, suggesting that sulfation of sialyl Lewis X moiety was the cause of the discrepancy in the reactivity of the anti-sialyl Lewis X antibodies. When tested against various authentic sulfated sialyl Lewis X determinants, 6-sulfo sialyl Lewis X and 6,6'-bis-sulfo sialyl Lewis X were found to be reactive to the antibodies, 2F3, 2H5 and HECA-452, but not with antibodies FH-6 and CSLEX-1, suggesting that the distinct type of sialyl Lewis X determinant on the HEV endothelial cells and Fuc-T VII-transfected endothelial cell clone are mainly 6-sulfo and/or 6,6'-bis-sulfo sialyl Lewis X determinants.     

Beta-decay half-lives calculated on the gross theory

Beta-decay half-lives have been calculated by the use of the gross theory which was formulated by Takahashi, Yamada, and Koyama. Both allowed and first-forbidden transitions have been taken into account, and consideration also has been given to the possibility that all the transitions to the levels near the ground states may be highly forbidden. The Q-values used in the calculation have been taken from the mass formula of Myers and Swiatecki. The calculated half-lives are shown in the PLOTS together with the experimental data and the Q-values. The PLOTS cover all the isotopes between the proton-drip and neutron-drip lines with Z = 3 to Z = 100.     

On norm bounds for algebraic Riccati and Lyapunov equations

New lower bounds on the spectral norms of the positive definite solutions to the continuos and discrete algebraic matrix Riccati and Lyapunov equations are derived. These bounds are much easier to compute than previously available bounds and appear to be considerably tighter in many cases.     

A surface acoustic wave on a ferroelectric layer-structure oxide

As a piezoelectric application of a ferroelectric material of layer-structure type, a surface acoustic wave device using a ceramic Pb_0.15 (NaBi)_0.425Bi₄Ti₄O₁₅, produced by a hot-forging technique is described. The surface acoustic wave on the substrate with the poling axis parallel to the free surface is Blustein-Gulyaev type and its velocity is 2812 m/s.     

Radar cross-section measurement method using a spatial filtering within a near zone

A spatial filtering is a useful method for suppressing unwanted reflection from undesired scatters on radar cross-section (RCS) measurements. Highly accurate RCS measurements for stealth-designed targets are generally performed by using full-scale models. However, it is difficult to carry out a measurement of a large full-scale target, because a vast RCS measurement site which satisfies the far-field criterion without undesired scatters is required. In this paper, we have applied the filtering method to RCS measurements in a near field and investigated the validity of that method by varying the scanning angular span. First, a distribution of scattering sources including undesired scatters is predicted from near-field spherical- or cylindrical-scanning data. Next, undesired scatters are suppressed using the spatial filtering. Finally, RCS values of the test target are calculated by taking the Fourier transform of the filtered scattering source distribution. Using electromagnetic simulations, we have validated the RCS measurement method by comparing predicted RCS with reference data as far-field RCS of the test target. As a result, predicted RCS profiles closely matched with reference data. In conclusion, the proposed method is useful for RCS measurements within the unsuitable near zone. Copyright © 2009 Institute of Electrical Engineers of Japan. Published by John Wiley & Sons, Inc.     

Alkoxyresorufin O-dealkylase assay using a rat hepatocyte spheroid microarray

Hepatocyte multicellular aggregates (spheroids), which maintain high expression of liver functions, have been advocated as a useful culture technique for various cell-based assays. In this study, we investigated the drug metabolic function of a hepatocyte spheroid microarray (HSM) chip, which contained an array of 672 spheroids of primary rat hepatocytes within a 100-mm² region in the center of a poly(methylmethacrylate) plate (24 × 24 mm) and used an alkoxyresorufin (ethoxy-, methoxy-, pentoxy- and benzyloxyresorufin) O-dealkylase assay system. Ethoxyresorufin O-dealkylase (EROD) activity of the HSM chip initiated by 3-methylcholanthrene (3-MC), an inducer of cytochrome P450 enzymes, was 5- to 10-fold higher than that of monolayer hepatocytes, with activity being maintained for at least 2 weeks. We also demonstrated that 3-MC induced EROD, methoxyresorufin O-dealkylase (MROD) and benzyloxyresorufin O-dealkylase (BROD) activities in the HSM chip, while sodium phenobarbital (P450 inducer) induced pentoxyresorufin O-dealkylase (PROD), BROD, EROD and MROD activities. Induction of these activities was confirmed by increased gene expression of the related P450 enzymes. These results showed that the HSM chip had a good response to P450 inducers and that function was maintained for long periods of time. The HSM chip therefore may be a promising cellular platform for drug metabolic assays using hepatocytes.     

Production of nonproteinaceous amino acids using recombinant Escherichia coli cells expressing cysteine synthase and related enzymes with or without the secretion of O-acetyl-L-serine

Beta-(pyrazol-1-yl)-L-alanine (beta-PA), a model nonproteinaceous amino acid, was specifically synthesized by two methods using recombinant Escherichia coli cells that express cysteine synthase, comprising serine acetyltransferase (SAT) and O-acetylserine sulfhydrylase-A (OASS-A) and related enzymes from E. coli. In the first method (method A), recombinant cells that express wild-type SAT, OASS-A, acetate kinase (AK), and phosphotransacetylase (PTA) showed the highest beta-PA production. beta-PA was produced at 140 mM from 200 mM L-serine and 200 mM pyrazole under optimum conditions. Using the cells expressing SATDeltaC20 (truncated SAT), OASS-A, AK, and PTA, beta-PA was produced at a level of only 80 mM, whereas O-acetyl-serine (OAS) was found to be secreted into the broth. Under optimum conditions, OAS accumulated at levels of around 105 mM from 300 mM L-serine. Thus, in the second method (method B), the secreted OAS was used as the substrate for the syntheses of beta-PA and beta-(triazol-1-yl)-L-alanine (beta-TA). The OAS that accumulated in the broth was efficiently converted to beta-PA and beta-TA at levels of around 90 mM from 105 mM OAS using free OASS-A. In both methods A and B, the addition of glucose was essential for the efficient production of beta-PA and OAS, respectively.     

Angiotensin I-Converting Enzyme Inhibitory Effect of Chinese Soypaste Along Fermentation and Ripening: Contribution of Early Soybean Protein Borne Peptides and Late Maillard Reaction Products

Angiotensin I-converting enzyme inhibitory effect of Chinese soypaste was investigated during 4-month fermentation and ripening. This effect increased significantly at early stage and reached a plateau until the end of ripening, with an IC₅₀ value of 0.436 mg/mL for the final product. Peptide and reducing sugar contents increased drastically during early fermentation and declined afterward. Maillard reaction took place continuously as indicated by consistent accumulation of precursor, intermediate, and final Maillard reaction products monitored by fluorescence, ultraviolet-absorbance and absorbance at 420 nm, respectively. During early fermentation, peptides were principal compounds responsible for the angiotensin I-converting enzyme inhibitory effect. During late ripening, angiotensin I-converting enzyme inhibition by Maillard reaction products could compensate for the loss of the effect caused by the utilization of peptides, and enable the total effect to remain at a good and steady level, suggesting an indispensable contribution of Maillard reaction products to angiotensin I-converting enzyme inhibitory effect of soypaste, particularly in products with prolonged maturation.