Compositional analysis and biological characterization of Cornus officinalis on human 1.1B4 pancreatic β cells

Arielle E Sharp-Tawfik1, Alexis M Coiner1, Catherine B MarElia1

  • 1Department of Cell Biology, Microbiology and Molecular Biology, University of South Florida, 4202 East Fowler Avenue, Tampa, FL 33620, USA.

Insights

Cornus officinalis (CO) may offer a novel therapy for early-stage Type 1 diabetes (T1D). This study shows CO protects pancreatic beta cells from death, enhances their function, and boosts energy metabolism, suggesting potential for T1D intervention.

Area of Science:

  • Immunology
  • Endocrinology
  • Pharmacology

Background:

  • Type 1 diabetes (T1D) is an autoimmune disease characterized by pancreatic beta cell destruction.
  • Current T1D therapies focus on insulin replacement, highlighting the need for interventions to protect residual beta cells.
  • Cornus officinalis (CO), used in Traditional Chinese Medicine, exhibits anti-inflammatory and pro-metabolic properties.

Purpose of the Study:

  • To investigate the potential of Cornus officinalis (CO) as an interventional therapy for early-stage Type 1 diabetes (T1D).
  • To determine if CO can protect pancreatic beta cells from cytokine-induced apoptosis and enhance their function.

Main Methods:

  • Cytokine-mediated beta cell death assays.
  • Cell viability and oxidative capacity measurements.
  • High-Performance Liquid Chromatography/Mass Spectrometry (HPLC/MS) for CO component profiling.
  • Analysis of Nuclear Factor of Activated T Cells, Cytoplasmic 2 (NFATC2) expression.

Main Results:

  • CO treatment inhibited cytokine-induced beta cell death.
  • CO increased beta cell viability, oxidative capacity, and energy metabolism.
  • CO induced the NFAT pathway, suggesting enhanced proliferation and endocrine function.
  • Bioactive components of CO were successfully profiled using HPLC/MS.

Conclusions:

  • Cornus officinalis (CO) demonstrates protective effects on pancreatic beta cells against inflammatory damage.
  • CO enhances beta cell energy metabolism and promotes pathways associated with proliferation and function.
  • CO presents a promising candidate for future interventional therapies in early-stage Type 1 diabetes.

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