κ-Carrageenan oligosaccharides induce microglia autophagy through AMPK/ULK1 pathway to regulate their immune response

Int J Biol Macromol. 2022 Jan 1:194:198-203. doi: 10.1016/j.ijbiomac.2021.11.191. Epub 2021 Dec 3.

Abstract

Microglia are the main effector cells of immune response in central nervous system and are important targets for disease prevention and treatment. Κ-carrageenan Oligosaccharide (KOS), obtained by enzymatic hydrolysis from carrageenan of marine red algae, can inhibit the release of inflammatory factors from the over-activated microglia. The mechanism of microglia autophagy induced by KOS and its relationship with inflammation were studied to explore the development prospect of KOS in the research and treatment of inflammatory related diseases. The effect of KOS on inducing autophagy was detected by the secretion of cytokines by lipopolysaccharide (LPS)-activated microglia, respectively. The protein expression of autophagy-related signaling pathways were detected by Western Blot. The results showed that KOS could significantly protect the microglia from over-activated inflammatory by inducing the autophagy and inhibiting the release of inflammatory cytokines. And KOS could reduce the expression of the protein that related to the AMPK/ULK1 pathways in microglia, so as to regulate the autophagy pathway, and inhibit the inflammatory response of over-activated microglia. The study on the effect of KOS on microglia autophagy and excessive inflammatory response will provide a theoretical basis for further studies on the inhibition of nerve injury by regulating microglia autophagy and inflammatory response.

Keywords: AMPK/ULK1; Autophagy; Cytokine; Inflammation; Microglia; Κ-carrageenan oligosaccharides.

MeSH terms

  • AMP-Activated Protein Kinases / metabolism*
  • Animals
  • Autophagy / drug effects*
  • Autophagy-Related Protein-1 Homolog / metabolism*
  • Biomarkers
  • Carrageenan / pharmacology*
  • Immunity / drug effects*
  • Inflammation Mediators
  • Mice
  • Microglia / drug effects*
  • Microglia / metabolism*
  • Signal Transduction / drug effects

Substances

  • Biomarkers
  • Inflammation Mediators
  • Carrageenan
  • Autophagy-Related Protein-1 Homolog
  • AMP-Activated Protein Kinases