183 research outputs found
ON THE MODULE CATEGORIES OF GENERALIZED PREPROJECTIVE ALGEBRAS OF DYNKIN TYPE
For a symmetrizable GCM C and its symmetrizer D, Geiss-Leclerc-SchrĀØoer [Invent. Math. 209 (2017)] has introduced a generalized preprojective algebra Ī associated to C and D, that contains a class of modules, called locally free modules. We show that any basic support Ļ- tilting Ī -module is locally free and gives a classification theorem of torsion-free classes in repĪ as the generalization of the work of Mizuno [Math. Z. 277 (2014)]
Deformed Cartan matrices and generalized preprojective algebras I: Finite type
We give an interpretation of the -deformed Cartan matrices of finite
type and their inverses in terms of bigraded modules over the generalized
preprojective algebras of Langlands dual type in the sense of
Gei\ss-Leclerc-Schr\"{o}er [Invent. math. 209 (2017)]. As an application, we
compute the first extension groups between the generic kernels introduced by
Hernandez-Leclerc [J. Eur. Math. Soc. 18 (2016)], and propose a conjecture that
their dimensions coincide with the pole orders of the normalized -matrices
between the corresponding Kirillov-Reshetikhin modules.Comment: 41 pages, v3: changed the title, minor corrections and added
explanations, updated reference
Copper-catalyzed reaction of aziridine for the synthesis of substituted imidazolidine and imidazolidinone
Herein we report a copper-catalyzed synthesis of imidazolidine by employing the reaction of aziridine with imine. The reaction smoothly provided a diverse range of 2-substituted imidazolidines with high compatibility with various functional groups. Moreover, during our investigation, we discovered that isocyanate also reacted with aziridine to yield substituted imidazolidinones efficiently. The versatility of these reactions was further demonstrated by their application in the synthesis of hybrid molecules derived from two pharmaceutical compounds. This approach opens new possibilities for the discovery of novel classes of bioactive molecules
Tumorigenesis of EpsteināBarr Virus-Positive Epithelial Cell Lines Derived from Gastric Tissues in the SCID Mouse
AbstractTo study the tumorigenesis of EpsteināBarr virus (EBV)-positive epithelial cell lines GT38 and GT39 derived from human gastric tissues, we inoculated these cells under the skin of severe combined immunodeficient (SCID) mice. The development of tumors was observed in each of the mice about 2 months after the inoculation. The tumors were diagnosed with undifferentiated carcinoma by hematoxylin/eosin staining. EBV-encoded small RNA1 was detected in the paraffin-embedded tumor sections. The tumor cells had human chromosome. The circular, but not linear, EBV DNA was detected in the tumors. The molecular sizes of EBV DNA termini were the same as that of the inoculated GT38 or GT39 cells. The expressions of EBV nuclear antigen 2 and latent membrane protein 1 reduced in the tumors. Transcripts of BamHI C and W promoters in latency III were detected in the tumors and the cultured cells in vitro. The tumor cells were passaged from one SCID mouse to other SCID mice and to cultures in vitro. This is the first evidence that the EBV-positive epithelial cell lines produced tumors in the SCID mouse
Phytoceramide and sphingoid bases derived from brewer's yeast Saccharomyces pastorianus activate peroxisome proliferator-activated receptors
<p>Abstract</p> <p>Background</p> <p>Peroxisome proliferator-activated receptors (PPARs) are ligand-activated transcription factors that regulate lipid and glucose metabolism. PPARĪ± is highly expressed in the liver and controls genes involved in lipid catabolism. We previously reported that synthetic sphingolipid analogs, part of which contains shorter-length fatty acid chains than natural sphingolipids, stimulated the transcriptional activities of PPARs. Sphingosine and dihydrosphingosine (DHS) are abundant sphingoid bases, and ceramide and dihydroceramide are major ceramide species in mammals. In contrast, phytosphingosine (PHS) and DHS are the main sphingoid bases in fungi. PHS and phytoceramide exist in particular tissues such as the epidermis in mammals, and involvement of ceramide species in PPARĪ² activation in cultured keratinocytes has been reported. The purpose of the present study is to investigate whether natural sphingolipids with C18 fatty acid and yeast-derived sphingoid bases activate PPARs as PPAR agonists.</p> <p>Method</p> <p>Lipids of brewer's yeast contain PHS- and DHS-based sphingolipids. To obtain the sphingoid bases, lipids were extracted from brewer's yeast and acid-hydrolyzed. The sphingoid base fraction was purified and quantified. To assess the effects of sphingolipids on PPAR activation, luciferase reporter assay was carried out. NIH/3T3 and human hepatoma (HepG2) cells were transfected with expression vectors for PPARs and retinoid Ć receptors, and PPAR responsive element reporter vector. When indicated, the PPAR/Gal4 chimera system was performed to enhance the credibility of experiments. Sphingolipids were added to the cells and the dual luciferase reporter assay was performed to determine the transcriptional activity of PPARs.</p> <p>Results</p> <p>We observed that phytoceramide increased the transcriptional activities of PPARs significantly, whereas ceramide and dihydroceramide did not change PPAR activities. Phytoceramide also increased transactivation of PPAR/Gal4 chimera receptors. Yeast-derived sphingoid base fraction, which contained PHS and DHS, or authentic PHS or DHS increased PPAR-dependent transcription. Additionally, phytoceramide stimulated PPARĪ± activity in HepG2 hepatocytes, suggesting that phytoceramide activates genes regulated by PPARĪ±.</p> <p>Conclusions</p> <p>Phytoceramide and yeast-derived sphingoid bases activate PPARs, whereas ceramide and dihydroceramide do not change the PPAR activity. The present findings suggest that phytoceramide acts as a PPAR ligand that would regulate PPAR-targeted genes.</p
SUBSTITUTION OF HIGH-PRESSURE CHARGE BY ELECTROLYSIS CHARGE AND HYDROGEN ENVIRONMENT EMBRITTLEMENT SUSCEPTIBILITIES FOR INCONEL 625 AND SUS 316L
Fracture strain in Inconel 625 decreases as hydrogen content charged by electrolysis increases, whereas that in SUS 316L does not change regardless of the hydrogen content of 161.5 mass ppm. Grain boundary fracture is observed on the surface of Inconel 625 absorbing a hydrogen content of 27.5 mass ppm, which corresponds to 59.2 MPa hydrogen gas at R.T using Sieverts law. In contrast, the fracture surfaces of SUS 316L hydrogen-charged at extremely high fugacities remain ductile dimples. Thus, hydrogen degradation susceptibility is much lower for SUS 316L than for Inconel 625
Integrated analysis of the oral and intestinal microbiome and metabolome of elderly people with more than 26 original teeth: a pilot study
Elderly subjects with more than 20 natural teeth have a higher healthy life expectancy than those with few or no teeth. The oral microbiome and its metabolome are associated with oral health, and they are also associated with systemic health via the oral-gut axis. Here, we analyzed the oral and gut microbiome and metabolome profiles of elderly subjects with more than 26 natural teeth. Salivary samples collected as mouth-rinsed water and fecal samples were obtained from 22 healthy individuals, 10 elderly individuals with more than 26 natural teeth and 24 subjects with periodontal disease. The oral microbiome and metabolome profiles of elderly individuals resembled those of subjects with periodontal disease, with the metabolome showing a more substantial differential abundance of components. Despite the distinct oral metabolome profiles, there was no differential abundance of components in the gut microbiome and metabolomes, except for enrichment of short-chain fatty acids in elderly subjects. Finally, to investigate the relationship between the oral and gut microbiome and metabolome, we analyzed bacterial coexistence in the oral cavity and gut and analyzed the correlation of metabolite levels between the oral cavity and gut. However, there were few associations between oral and gut for bacteria and metabolites in either elderly or healthy subjects. Overall, these results indicate distinct oral microbiome and metabolome profiles, as well as the lack of an oral-gut axis in elderly subjects with a high number of natural teeth
Drift effects and the cosmic ray density gradient in a solar rotation period: First observation with the Global Muon Detector Network (GMDN)
We present for the first time hourly variations of the spatial density
gradient of 50 GeV cosmic rays within a sample solar rotation period in 2006.
By inversely solving the transport equation, including diffusion, we deduce the
gradient from the anisotropy that is derived from the observation made by the
Global Muon Detector Network (GMDN). The anisotropy obtained by applying a new
analysis method to the GMDN data is precise and free from atmospheric
temperature effects on the muon count rate recorded by ground based detectors.
We find the derived north-south gradient perpendicular to the ecliptic plane is
oriented toward the Helioshperic Current Sheet (HCS) (i.e. southward in the
toward sector of the Interplanetary Magnetic Field (IMF) and northward in the
away sector). The orientation of the gradient component parallel to the
ecliptic plane remains similar in both sectors with an enhancement of its
magnitude seen after the Earth crosses the HCS. These temporal features are
interpreted in terms of a local maximum of the cosmic ray density at the HCS.
This is consistent with the prediction of the drift model for the epoch.
By comparing the observed gradient with the numerical prediction of a simple
drift model, we conclude that particle drifts in the large-scale magnetic field
play an important role in organizing the density gradient, at least in the
present epoch. We also found that corotating interaction regions did not
have such a notable effect. Observations with the GMDN provide us with a new
tool for investigating cosmic ray transport in the IMF.Comment: 35 pages, 10 figures, submitted to the Astrophysical Journa
miR-199a-3p inhibits cell proliferation and induces apoptosis by targeting YAP1, suppressing Jagged1-Notch signaling in human hepatocellular carcinoma
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