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1.
Shigeyoshi Fujiwara Ken-Ichi Imadome Masami Takei 《Experimental & molecular medicine》2015,47(1):e135
The development of highly immunodeficient mouse strains has allowed the reconstitution of functional human immune system components in mice. New-generation humanized mice generated in this manner have been extensively used for modeling viral infections that are exclusively human tropic. Epstein–Barr virus (EBV)-infected humanized mice reproduce cardinal features of EBV-associated B-cell lymphoproliferative disease and EBV-associated hemophagocytic lymphohistiocytosis (HLH). Erosive arthritis morphologically resembling rheumatoid arthritis (RA) has also been recapitulated in these mice. Low-dose EBV infection of humanized mice results in asymptomatic, persistent infection. Innate immune responses involving natural killer cells, EBV-specific adaptive T-cell responses restricted by human major histocompatibility and EBV-specific antibody responses are also elicited in humanized mice. EBV-associated T-/natural killer cell lymphoproliferative disease, by contrast, can be reproduced in a distinct mouse xenograft model. In this review, recent findings on the recapitulation of human EBV infection and pathogenesis in these mouse models, as well as their application to preclinical studies of experimental anti-EBV therapies, are described. 相似文献
2.
Furuta Etsuko Akiyama Kazuhiko Inoue Hiroyoshi Kataoka Yasuhide Sensui Masaaki 《Journal of Radioanalytical and Nuclear Chemistry》2020,324(1):109-122
Journal of Radioanalytical and Nuclear Chemistry - A new dipping method was studied for the measurement of radioactive solution using plastic scintillator sheets and pellets (PSs) and a liquid... 相似文献
3.
Arylpyrrolyldiketone boron complexes as anion‐responsive π‐electronic molecules were synthesized by Claisen condensations of acetylpyrrole and corresponding aryl esters. The synthesized π‐electronic molecules exhibited anion‐binding behavior with various binding modes including pyrrole‐inverted and non‐inverted [1+1]‐type anion complexes as well as [2+1]‐type complexes owing to the presence of only a single pyrrole ring. Furthermore, solid‐state ion‐pairing assemblies, comprising receptor–anion complexes and countercations, were constructed based on fairly planar [2+1]‐type complexes. 相似文献
4.
Prof. Dr. Hiroyoshi Takamura Takayuki Fujiwara Yohei Kawakubo Prof. Dr. Isao Kadota Prof. Dr. Daisuke Uemura 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(6):1979-1983
Stereoselective and streamlined synthesis of the proposed C79–C104 fragment 2 of symbiodinolide ( 1 ), a polyol marine natural product with a molecular weight of 2860, was achieved. In the synthetic route, the proposed C79–C104 fragment 2 was synthesized by utilizing a Julia–Kocienski olefination and subsequent Sharpless asymmetric dihydroxylation as key transformations in a convergent manner. Detailed comparison of the 13C NMR chemical shifts between the natural product and the synthetic C79–C104 fragment 2 revealed that the stereostructure at the C91–C99 carbon chain moiety of symbiodinolide ( 1 ) should be reinvestigated. 相似文献
5.
6.
Hiroki Hasegawa Daisuke Sakamaki Hideki Fujiwara 《Angewandte Chemie (International ed. in English)》2023,62(26):e202302498
In this work, we aimed to develop a dicyanomethyl radical that undergoes both reversible C−C bond formation/dissociation and metal-ligand coordination reactions to combine dynamic covalent chemistry (DCC) based on organic radicals with coordination chemistry. We have previously reported a dicyanomethyl radical conjugated with a triphenylamine ( 1 ⋅) that exhibits a monomer/dimer equilibrium between the σ-bonded dimer ( 12 ). We designed and synthesized a novel dicyanomethyl radical with a pyridyl group as a coordination point ( 2 ⋅) by replacing the phenyl group of 1 ⋅ with a 3-pyridyl group. We showed that 2 ⋅ is also in an equilibrium with the σ-bonded dimer ( 22 ) in solution and has suitable thermodynamic parameters for application in DCC. 22 coordinates to PdCl2 in a 2 : 2 ratio to selectively form a metallamacrocycle ( 22 )2(PdCl2)2, and its structure was clarified by single crystal X-ray analysis. Variable-temperature NMR, ESR, and electronic absorption measurements revealed that ( 22 )2(PdCl2)2 also undergoes the reversible C−C bond formation/dissociation reaction. Ligand-exchange experiment showed that 22 was liberated from ( 22 )2(PdCl2)2 by the addition of another ligand with a higher affinity for PdII. This work demonstrated that DCC based on dicyanomethyl radicals works orthogonally to metal-ligand coordination reactions. 相似文献
7.
Hiroki Yamamoto Takuya Fujiwara Takashi Funatsu Makoto Tsunoda 《Molecules (Basel, Switzerland)》2021,26(8)
Biothiols, such as cysteine and glutathione, play important roles in various intracellular reactions represented by the redox equilibrium against oxidative stress. In this study, a method for intracellular thiol quantification using HPLC-fluorescence detection was developed. Thiols were derivatized with a thiol-specific fluorescence derivatization reagent, viz. ammonium 7-fluoro-2,1,3-benzoxadiazole-4-sulfonate (SBD-F), followed by reversed-phase separation on an InertSustain AQ-C18 column. Six different SBD-thiols (homocysteine, cysteine, cysteinylglycine, γ-glutamylcysteine, glutathione, and N-acetylcysteine as an internal standard) were separated within 30 min using a citric buffer (pH 3.0)/MeOH mobile phase. The calibration curves of all the SBD-thiols had strong linearity (R2 > 0.999). Using this developed method, the thiol concentrations of human chronic myelogenous leukemia K562 cell samples were found to be 5.5–153 pmol/1 × 106 cells. The time-dependent effect of a thiol scavenger, viz. N-ethyl maleimide, on intracellular thiol concentrations was also quantified. This method is useful for elucidating the role of intracellular sulfur metabolism. 相似文献
8.
Jinhua Hong Shunsuke Kobayashi Akihide Kuwabara Yumi H. Ikuhara Yasuyuki Fujiwara Yuichi Ikuhara 《Molecules (Basel, Switzerland)》2021,26(12)
Solid electrolytes, such as perovskite Li3xLa2/1−xTiO3, LixLa(1−x)/3NbO3 and garnet Li7La3Zr2O12 ceramic oxides, have attracted extensive attention in lithium-ion battery research due to their good chemical stability and the improvability of their ionic conductivity with great potential in solid electrolyte battery applications. These solid oxides eliminate safety issues and cycling instability, which are common challenges in the current commercial lithium-ion batteries based on organic liquid electrolytes. However, in practical applications, structural disorders such as point defects and grain boundaries play a dominating role in the ionic transport of these solid electrolytes, where defect engineering to tailor or improve the ionic conductive property is still seldom reported. Here, we demonstrate a defect engineering approach to alter the ionic conductive channels in LixLa(1−x)/3NbO3 (x = 0.1~0.13) electrolytes based on the rearrangements of La sites through a quenching process. The changes in the occupancy and interstitial defects of La ions lead to anisotropic modulation of ionic conductivity with the increase in quenching temperatures. Our trial in this work on the defect engineering of quenched electrolytes will offer opportunities to optimize ionic conductivity and benefit the solid electrolyte battery applications. 相似文献
9.
Dr. Akihiro Takada Hiroaki Fujiwara Dr. Kenji Sugimoto Dr. Hirofumi Ueda Prof. Dr. Hidetoshi Tokuyama 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(46):16400-16403
The total synthesis of (?)‐isoschizogamine was accomplished, featuring the construction of the quaternary carbon center by the modified Johnson–Claisen rearrangement in basic media and the facile assembly of the key tetracyclic quinolone intermediate through a cascade cyclization. The characteristic cyclic aminal was constructed by late‐stage C?H functionalization at the position adjacent to the lactam nitrogen using a combination of CrO3 and nBu4NIO4 and subsequent Bi(OTf)3‐mediated cyclization. 相似文献
10.
Radiation emitted from the shock layer generated around a hypersonic flight model is experimentally investigated by using a ballistic range (two-stage light-gas gun). A polyethylene projectile of 1.2 cm in diameter is launched in this facility at the velocity of 5 km/sec (M=15), and the emission from the induced shock layer around the projectile is observed with a spectroscope. As a result, molecular band-spectra from NO and N2 are detected along with those from carboncontaining molecules. Total emission power is measured with a diode-type powermeter. In addition, dimension effect of the flight model is theoretically and numerically examined, and a scaling law on thermochemical structure of the shock layer is developed. It shows that the thickness of thermal boundary-layer formed on the model surface does not follow the conventional scaling law based on the reaction distance and on the energy relaxation distance. Finally, the radiative field around the projectile is numerically computed, and the total power emitted from the shock layer is estimated. From the comparison between computed and measured results, the validity of the calculation model is discussed. 相似文献