Publications by authors named "Touya Toyomoto"

Article Synopsis
  • Interferons (IFNs) are cytokines produced by immune cells that have significant roles in combating viruses and tumors, with key subclasses including type-I (IFN-α and IFN-β) and type-II (IFN-γ) that activate different receptors.
  • Previous research indicated that supersulfide donors, specifically N-acetyl-L-cysteine tetrasulfide (NAC-S2), can suppress IFN-β-induced responses in macrophages, particularly affecting the phosphorylation of STAT1.
  • This study discovered that NAC-S2 also inhibits IFN-α/β and IFN-γ signaling by blocking Janus kinases (JAKs), and suggested that understanding the molecular mechanisms behind these
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A principal concept in developing antibacterial agents with selective toxicity is blocking metabolic pathways that are critical for bacterial growth but that mammalian cells lack. Serine -acetyltransferase (CysE) is an enzyme in many bacteria that catalyzes the first step in l-cysteine biosynthesis by transferring an acetyl group from acetyl coenzyme A (acetyl-CoA) to l-serine to form -acetylserine. Because mammalian cells lack this l-cysteine biosynthesis pathway, developing an inhibitor of CysE has been thought to be a way to establish a new class of antibacterial agents.

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Infection of mice with Citrobacter rodentium is a useful model for studying the pathogenicity of enteropathogenic and enterohemorrhagic Escherichia coli, pathogens that have a close association with humans. Here, we provide a protocol detailing the approaches for non-canonical inflammasome analysis in a mouse model of C. rodentium infection, including preparation of bacteria, oral administration of bacteria to mice, counting colony-forming units to quantify bacterial colonization, and analysis of expression and activation of inflammasome-related factors.

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Pseudomonas aeruginosa is a Gram-negative opportunistic pathogen that presents a serious risk to immunosuppressed individuals and other extremely vulnerable patients such as those in intensive care units. The emergence of multidrug-resistant Pseudomonas strains has increased the need for new antipseudomonal agents. In this study, a series of amino group-modified aminopenicillin derivatives was synthesized that have different numbers of carboxyl groups and structurally resemble carboxypenicillin-ureidopenicillin hybrids, and their antipseudomonal activities were evaluated.

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