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Träfflista för sökning "WFRF:(Kitagawa Hiroshi) "

Sökning: WFRF:(Kitagawa Hiroshi)

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1.
  • Bergefall, Kicki, 1975, et al. (författare)
  • Chondroitin sulfate characterized by the E-disaccharide unit is a potent inhibitor of herpes simplex virus infectivity and provides the virus binding sites on gro2C cells.
  • 2005
  • Ingår i: The Journal of biological chemistry. - 0021-9258. ; 280:37, s. 32193-9
  • Tidskriftsartikel (refereegranskat)abstract
    • Although cell surface chondroitin sulfate (CS) is regarded as an auxiliary receptor for binding of herpes simplex virus to cells, and purified CS chain types A, B, and C are known to interfere poorly or not at all with the virus infection of cells, we have found that CS type E (CS-E), derived from squid cartilage, exhibited potent antiviral activity. The IC(50) values ranged from 0.06 to 0.2 mug/ml and substantially exceeded the antiviral potency of heparin, the known inhibitor of virus binding to cells. Furthermore, in mutant gro2C cells that express CS but not heparan sulfate, CS-E showed unusually high anti-herpes virus activity with IC(50) values of <1 ng/ml. Enzymatic degradation of CS-E with chondroitinase ABC abolished its antiviral activity. CS-E inhibited the binding to cells of the purified virus attachment protein gC. A direct interaction of gC with immobilized CS-E and inhibition of this binding by CS-E oligosaccharide fragments greater than octasaccharide were demonstrated. Likewise, the gro2C-specific CS chains interfered with the binding of viral gC to these cells and were found to contain a considerable proportion (13%) of the E-disaccharide unit, suggesting that this unit is an essential component of the CS receptor for herpes simplex virus on gro2C cells and that the antiviral activity of CS-E was due to interference with the binding of viral gC to a CS-E-like receptor on the cell surface. Knowledge of the determinants of antiviral properties of CS-E will help in the development of inhibitors of herpes simplex virus infections in humans.
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2.
  • Morokuma, Tomoki, et al. (författare)
  • Kiso Supernova Survey (KISS) : Survey strategy
  • 2014
  • Ingår i: Nippon Tenmon Gakkai obun kenkyu hokoku. - : Oxford University Press (OUP). - 0004-6264. ; 66:6
  • Tidskriftsartikel (refereegranskat)abstract
    • lThe Kiso Supernova Survey (KISS) is a high-cadence optical wide-field supernova (SN) survey. The primary goal of the survey is to catch the very early light of a SN, during the shock breakout phase. Detection of SN shock breakouts combined with multi-band photometry obtained with other facilities would provide detailed physical information on the progenitor stars of SNe. The survey is performed using a 2 degrees.2 x 2 degrees.2 field-of-view instrument on the 1.05-m Kiso Schmidt telescope, the Kiso Wide Field Camera (KWFC). We take a 3-min exposure in g-band once every hour in our survey, reaching magnitude g similar to 20-21. About 100 nights of telescope time per year have been spent on the survey since 2012 April. The number of the shock breakout detections is estimated to be of the order of 1 during our three-year project. This paper summarizes the KISS project including the KWFC observing setup, the survey strategy, the data reduction system, and CBET-reported SNe discovered so far by KISS.
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3.
  • Uyama, Toru, et al. (författare)
  • Chondroitin 4-O-sulfotransferase-1 regulates E disaccharide expression of chondroitin sulfate required for herpes simplex virus infectivity.
  • 2006
  • Ingår i: The Journal of biological chemistry. - 0021-9258. ; 281:50, s. 38668-74
  • Tidskriftsartikel (refereegranskat)abstract
    • We have demonstrated a defect in expression of chondroitin 4-O-sulfotransferase-1 (C4ST-1) in murine sog9 cells, which are poorly sensitive to infection by herpes simplex virus type 1 (HSV-1). Sog9 cells were previously isolated as CS-deficient cells from gro2C cells, which were partially resistant to HSV-1 infection and defective in the expression of heparan sulfate (HS) because of a splice site mutation in the EXT1 gene encoding the HS-synthesizing enzyme. Here we detected a small amount of CS chains in sog9 cells with a drastic decrease in 4-O-sulfation compared with the parental gro2C cells. RT-PCR revealed that sog9 cells had a defect in the expression of C4ST-1 in addition to EXT1. Gel filtration analysis showed that the decrease in the amount of CS in sog9 cells was the result of a reduction in the length of CS chains. Transfer of C4ST-1 cDNA into sog9 cells (sog9-C4ST-1) restored 4-O-sulfation and amount of CS, verifying that sog9 cells had a specific defect in C4ST-1. Furthermore, the expression of C4ST-1 rendered sog9 cells significantly more susceptible to HSV-1 infection, suggesting that CS modified by C4ST-1 is sufficient for the binding and infectivity of HSV-1. Analysis of CS chains of gro2C and sog9-C4ST-1 cells revealed a considerable proportion of the E disaccharide unit, consistent with our recent finding that this unit is an essential component of the HSV receptor. These results suggest that C4ST-1 regulates the expression of the E disaccharide unit and the length of CS chains, the features that facilitate infection of cells by HSV-1.
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4.
  • Yanagisawa, Akihiro, et al. (författare)
  • Amyloid deposits derived from transthyretin in the ligamentum flavum as related to lumbar spinal canal stenosis.
  • 2015
  • Ingår i: Modern Pathology. - : Elsevier BV. - 0893-3952 .- 1530-0285. ; 28:2, s. 201-207
  • Tidskriftsartikel (refereegranskat)abstract
    • Amyloidosis is a protein conformational disorder with the distinctive feature of extracellular accumulation of amyloid fibrils that come from different proteins. In the ligamentum flavum of the lumbar spine, amyloid deposits were frequently found in elderly patients with lumbar spinal canal stenosis and were at least partially formed by wild-type transthyretin. However, how amyloid deposits in the ligamentum flavum affect lumbar spinal canal stenosis has remained unclear. In this study, we analyzed clinical, pathologic, and radiologic findings of patients with lumbar spinal canal stenosis who had amyloid deposits in the ligamentum flavum. We studied 95 ligamentum flavum specimens obtained from 56 patients with lumbar spinal canal stenosis and 21 ligamentum flavum specimens obtained from 19 patients with lumbar disk herniation. We evaluated histopathologic findings and clinicoradiologic manifestations, such as thickness of the ligamentum flavum and lumbar spinal segmental instability. We found that all 95 ligamentum flavum specimens resected from patients with lumbar spinal canal stenosis had amyloid deposits, which we classified into two types, transthyretin-positive and transthyretin-negative, and that transthyretin amyloid formation in the ligamentum flavum of patients with lumbar spinal canal stenosis was an age-associated phenomenon. The amount of amyloid in the ligamentum flavum was related to clinical manifestations of lumbar spinal canal stenosis, such as thickness of the ligamentum flavum and lumbar spinal segmental instability, in the patients with lumbar spinal canal stenosis with transthyretin-positive amyloid deposits. To our knowledge, this report is the first to show clinicopathologic correlations in transthyretin amyloid deposits of the ligamentum flavum. In conclusion, transthyretin amyloid deposits in the ligamentum flavum may be related to the pathogenesis of lumbar spinal canal stenosis in elderly patients.Modern Pathology advance online publication, 5 September 2014; doi:10.1038/modpathol.2014.102.
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5.
  • Zhang, Wei, et al. (författare)
  • A rapid method of simultaneous chromatographic purification of Li and Mg for isotopic analyses using MC-ICP-MS
  • 2022
  • Ingår i: International Journal of Mass Spectrometry. - : Elsevier. - 1387-3806 .- 1873-2798. ; 480
  • Tidskriftsartikel (refereegranskat)abstract
    • Lithium (Li) and Magnesium (Mg) isotopes have been widely used as valuable tracers to study geological processes. In general, several column separation procedures have been used to separate Li and Mg. In this study, we present an optimized protocol for the rapid and simultaneous purification of Li and Mg, which significantly reduces the separation time, required reagent volume, and procedural blanks compared to previous methods. Samples with small amounts of Li (generally 5 ng Li yielding Mg masses of 1 -1200 mu g) were separated, with the corresponding yields of Li and Mg being nearly 100%. Lithium and Mg isotope analyses were performed using an MC-ICP-MS (Thermo Scientific NEPTUNE Plus) and only <0.2 ng Li and <150 ng Mg were consumed for each analysis. Matrix-doping experiments reveal that the matrix effect is negligible for the determination of Li and Mg isotopes from a wide array of geological samples using our protocol. The robustness of the protocol has been validated by replicated analyses of standard solutions and geological standards, which yield long-term external 2 sigma precision better than +/- 0.6 parts per thousand for delta Li-7 and +/- 0.08 parts per thousand for delta Mg-26. Lithium and Mg isotopic ratios of all reference materials measured in this study agreed well with previous data within uncertainties. The method developed in this study allows for the rapid and high-purity separation of Li and Mg and subsequent high-precision isotopic analyses of these elements. (C) 2022 Elsevier B.V. All rights reserved.
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