Enzyme-Aided Extraction of Fucoidan by AMG Augments the Functionality of EPCs through Regulation of the AKT/Rheb Signaling Pathway

Mar Drugs. 2019 Jul 3;17(7):392. doi: 10.3390/md17070392.

Abstract

The purpose of the present study is to improve the endothelial progenitor cells (EPC) activation, proliferation, and angiogenesis using enzyme-aided extraction of fucoidan by amyloglucosidase (EAEF-AMG). Enzyme-aided extraction of fucoidan by AMG (EAEF-AMG) significantly increased EPC proliferation by reducing the reactive oxygen species (ROS) and decreasing apoptosis. Notably, EAEF-AMG treated EPCs repressed the colocalization of TSC2/LAMP1 and promoted perinuclear localization of mTOR/LAMP1 and mTOR/Rheb. Moreover, EAEF-AMG enhanced EPC functionalities, including tube formation, cell migration, and wound healing via regulation of AKT/Rheb signaling. Our data provided cell priming protocols to enhance therapeutic applications of EPCs using bioactive compounds for the treatment of CVD.

Keywords: amyloglucosidase; cell proliferation; endothelial progenitor cells; fucoidan; vascular regeneration.

MeSH terms

  • Apoptosis / drug effects
  • Cell Movement / drug effects
  • Cell Proliferation / drug effects
  • Cells, Cultured
  • Endothelial Progenitor Cells / drug effects*
  • Endothelial Progenitor Cells / metabolism
  • Glucan 1,4-alpha-Glucosidase / metabolism*
  • Humans
  • Lysosomal-Associated Membrane Protein 1 / metabolism
  • Neovascularization, Physiologic / drug effects
  • Polysaccharides / pharmacology*
  • Proto-Oncogene Proteins c-akt / metabolism*
  • Reactive Oxygen Species / metabolism
  • Signal Transduction / drug effects*
  • TOR Serine-Threonine Kinases / metabolism
  • Tuberous Sclerosis Complex 2 Protein / metabolism
  • Wound Healing / drug effects

Substances

  • Lysosomal-Associated Membrane Protein 1
  • Polysaccharides
  • Reactive Oxygen Species
  • Tuberous Sclerosis Complex 2 Protein
  • fucoidan
  • Proto-Oncogene Proteins c-akt
  • TOR Serine-Threonine Kinases
  • Glucan 1,4-alpha-Glucosidase