Search Results - "Uchiyama, Keiji"
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Neurotropic influenza A virus infection causes prion protein misfolding into infectious prions in neuroblastoma cells
Published in Scientific reports (12-05-2021)“…Misfolding of the cellular prion protein, PrP C , into the amyloidogenic isoform, PrP Sc , which forms infectious protein aggregates, the so-called prions, is…”
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Analysis of intracellular IgG secretion in Chinese hamster ovary cells to improve IgG production
Published in Journal of bioscience and bioengineering (01-01-2019)“…The production of biopharmaceutical immunoglobulin G (IgG) using cultured mammalian cells, especially Chinese hamster ovary (CHO) cells is well established and…”
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The N-Terminal Polybasic Region of Prion Protein Is Crucial in Prion Pathogenesis Independently of the Octapeptide Repeat Region
Published in Molecular neurobiology (01-02-2020)“…Conformational conversion of the cellular isoform of prion protein, designated PrP C , into the abnormally folded, amyloidogenic isoform, PrP Sc , is an…”
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Ethanolamine Is a New Anti-Prion Compound
Published in International journal of molecular sciences (29-10-2021)“…Prion diseases are a group of fatal neurodegenerative disorders caused by accumulation of proteinaceous infectious particles, or prions, which mainly consist…”
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Prions disturb post-Golgi trafficking of membrane proteins
Published in Nature communications (14-05-2013)“…Conformational conversion of normal cellular prion protein PrP C into pathogenic PrP Sc is central to the pathogenesis of prion diseases. However, the…”
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Prion protein protects mice from lethal infection with influenza A viruses
Published in PLoS pathogens (03-05-2018)“…The cellular prion protein, designated PrPC, is a membrane glycoprotein expressed abundantly in brains and to a lesser extent in other tissues. Conformational…”
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Prion protein signaling induces M2 macrophage polarization and protects from lethal influenza infection in mice
Published in PLoS pathogens (26-08-2020)“…The cellular prion protein, PrP.sup.C, is a glycosylphosphatidylinositol anchored-membrane glycoprotein expressed most abundantly in neuronal and to a lesser…”
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Structural and mechanistic aspects influencing the ADAM10-mediated shedding of the prion protein
Published in Molecular neurodegeneration (06-04-2018)“…Keywords: ADAM10, Antibody, Exosomes, Glycosylation, Membrane anchor, Neurodegeneration, Prion protein, Proteolytic cleavage, Shedding…”
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Secretion analysis of intracellular “difficult-to-express” immunoglobulin G (IgG) in Chinese hamster ovary (CHO) cells
Published in Cytotechnology (Dordrecht) (01-02-2019)“…The Chinese hamster ovary (CHO) cell line is the most widely used host cell for therapeutic antibody production. Although its productivity has been improved by…”
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Prions amplify through degradation of the VPS10P sorting receptor sortilin
Published in PLoS pathogens (30-06-2017)“…Prion diseases are a group of fatal neurodegenerative disorders caused by prions, which consist mainly of the abnormally folded isoform of prion protein,…”
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Vaporized Hydrogen Peroxide and Ozone Gas Synergistically Reduce Prion Infectivity on Stainless Steel Wire
Published in International journal of molecular sciences (23-03-2021)“…Prions are infectious agents causing prion diseases, which include Creutzfeldt-Jakob disease (CJD) in humans. Several cases have been reported to be…”
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Strain-Dependent Prion Infection in Mice Expressing Prion Protein with Deletion of Central Residues 91-106
Published in International journal of molecular sciences (01-10-2020)“…Conformational conversion of the cellular prion protein, PrP , into the abnormally folded isoform, PrP , is a key pathogenic event in prion diseases. However,…”
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Analysis of the immunoglobulin G (IgG) secretion efficiency in recombinant Chinese hamster ovary (CHO) cells by using Citrine-fusion IgG
Published in Cytotechnology (Dordrecht) (01-02-2019)“…Biopharmaceuticals represented by immunoglobulin G (IgG) are produced by the cultivation of recombinant animal cells, especially Chinese hamster ovary (CHO)…”
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Effects of prion protein devoid of the N-terminal residues 25-50 on prion pathogenesis in mice
Published in Archives of virology (01-07-2017)“…The N-terminal polybasic region of the normal prion protein, PrP C , which encompasses residues 23-31, is important for prion pathogenesis by affecting…”
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p37 Is a p97 Adaptor Required for Golgi and ER Biogenesis in Interphase and at the End of Mitosis
Published in Developmental cell (01-12-2006)“…We previously reported that p97/p47-assisted membrane fusion is important for the reassembly of organelles at the end of mitosis, but not for their maintenance…”
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Structural basis of the interaction between the AAA ATPase p97/VCP and its adaptor protein p47
Published in The EMBO journal (10-03-2004)“…The AAA ATPase p97/VCP is involved in many cellular events including ubiquitin‐dependent processes and membrane fusion. In the latter, the p97 adaptor protein…”
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p97/p47-Mediated Biogenesis of Golgi and ER
Published in Journal of biochemistry (Tokyo) (01-02-2005)“…In mammalian cells, the Golgi apparatus and endoplasmic reticulum have typical structures during interphase: stacked cisternae located adjacent to the nucleus…”
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Mouse-hamster chimeric prion protein (PrP) devoid of N-terminal residues 23-88 restores susceptibility to 22L prions, but not to RML prions in PrP-knockout mice
Published in PloS one (16-10-2014)“…Prion infection induces conformational conversion of the normal prion protein PrPC, into the pathogenic isoform PrPSc, in prion diseases. It has been shown…”
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VCIP135, a Novel Essential Factor for p97/p47-Mediated Membrane Fusion, Is Required for Golgi and ER Assembly in vivo
Published in The Journal of cell biology (09-12-2002)“…NSF and p97 are ATPases required for the heterotypic fusion of transport vesicles with their target membranes and the homotypic fusion of organelles. NSF uses…”
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Biological and biochemical characterization of mice expressing prion protein devoid of the octapeptide repeat region after infection with prions
Published in PloS one (21-08-2012)“…Accumulating lines of evidence indicate that the N-terminal domain of prion protein (PrP) is involved in prion susceptibility in mice. In this study, to…”
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