Tadatsugu Taniguchi

ORCID: 0000-0001-5212-090X
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Cytokine Signaling Pathways and Interactions
  • interferon and immune responses
  • Immune Response and Inflammation
  • Immune Cell Function and Interaction
  • NF-κB Signaling Pathways
  • T-cell and Retrovirus Studies
  • T-cell and B-cell Immunology
  • Immune cells in cancer
  • Monoclonal and Polyclonal Antibodies Research
  • RNA Research and Splicing
  • Inflammation biomarkers and pathways
  • RNA and protein synthesis mechanisms
  • Neutrophil, Myeloperoxidase and Oxidative Mechanisms
  • Animal Disease Management and Epidemiology
  • Cancer-related Molecular Pathways
  • Immunotherapy and Immune Responses
  • Virus-based gene therapy research
  • Bone Metabolism and Diseases
  • IL-33, ST2, and ILC Pathways
  • Cell Adhesion Molecules Research
  • Cell death mechanisms and regulation
  • RNA regulation and disease
  • Circular RNAs in diseases
  • Cancer-related molecular mechanisms research
  • Bacteriophages and microbial interactions

Kissei Pharmaceutical (Japan)
2025

Kanazawa University Hospital
2012-2025

The University of Tokyo
2015-2024

Advanced Institute of Industrial Technology
2023

Tokyo University of Science
1999-2020

Kanazawa University
1968-2016

Japan Science and Technology Agency
2010-2014

Takara (Japan)
2012

Intensive Care Society
2012

Nagasaki University
2005

CD4(+) T regulatory cells (T(regs)), which express the Foxp3 transcription factor, play a critical role in maintenance of immune homeostasis. Here, we show that mice, T(regs) were most abundant colonic mucosa. The spore-forming component indigenous intestinal microbiota, particularly clusters IV and XIVa genus Clostridium, promoted T(reg) cell accumulation. Colonization mice by defined mix Clostridium strains provided an environment rich transforming growth factor-β affected Foxp3(+) number...

10.1126/science.1198469 article EN Science 2010-12-24

A critical function of tumor suppressor p53 is the induction apoptosis in cells exposed to noxious stresses. We report a previously unidentified pro-apoptotic gene, Noxa . Expression primary mouse x-ray irradiation was dependent on p53. encodes Bcl-2 homology 3 (BH3)–only member family proteins; this contains BH3 region but not other BH domains. When ectopically expressed, underwent motif–dependent localization mitochondria and interacted with anti-apoptotic members, resulting activation...

10.1126/science.288.5468.1053 article EN Science 2000-05-12

The mitogen-activated protein kinase (MAPK) pathway is a conserved eukaryotic signaling module that converts receptor signals into various outputs. MAPK activated through phosphorylation by (MAPKK), which first MAPKK (MAPKKK). A genetic selection based on in yeast was used to identify mouse (TAK1) distinct from other members of the MAPKKK family. TAK1 shown participate regulation transcription transforming growth factor-beta (TGF-beta). Furthermore, activity stimulated response TGF-beta and...

10.1126/science.270.5244.2008 article EN Science 1995-12-22

Interleukin-6 (IL-6/BSF-2/IFNβ 2) is a multifunctional cytokine that regulates the growth and differentiation of various tissues, known particularly for its role in immune response acute phase reactions. A complementary DNA encoding human IL-6 receptor (IL-6-R) has now been isolated. The IL-6-R consists 468 amino acids, including signal peptide ∼19 acids domain ∼90 similar to immunoglobulin (Ig) superfamily. cytoplasmic ∼82 lacks tyrosine/kinase domain, unlike other factor receptors.

10.1126/science.3136546 article EN Science 1988-08-12

In mice lacking the interleukin-2 receptor beta chain (IL-2R beta), T cells were shown to be spontaneously activated, resulting in exhaustive differentiation of B into plasma and appearance high serum concentrations immunoglobulins G1 E as well autoantibodies that cause hemolytic anemia. Marked infiltrative granulocytopoiesis was also apparent, animals died after about 12 weeks. Depletion CD4+ mutant rescued without reversion granulocyte abnormalities. did not proliferate response polyclonal...

10.1126/science.7770771 article EN Science 1995-06-09

Production of nitric oxide (NO) by macrophages is important for the killing intracellular infectious agents. Interferon (IFN)- γ and lipopolysaccharide stimulate NO production transcriptionally up-regulating inducible synthase (iNOS). Macrophages from mice with a targeted disruption IFN regulatory factor-1 (IRF-1) gene (IRF-1 -/- mice) produced little or no synthesized barely detectable iNOS messenger RNA in response to stimulation. Two adjacent IRF-1 elements were identified promoter....

10.1126/science.7510419 article EN Science 1994-03-18
Coming Soon ...