Mannan oligosaccharide requires functional ETC and TLR for biological radiation protection to normal cells

BMC Cell Biol. 2018 Jun 27;19(1):9. doi: 10.1186/s12860-018-0161-4.

Abstract

Background: Low LET Ionizing radiation is known to alter intracellular redox balance by inducing free radical generation, which may cause oxidative modification of various cellular biomolecules. The extent of biomolecule-modifications/ damages and changes in vital processes (viz. cellular homeostasis, inter-/intra-cellular signaling, mitochondrial physiology/dynamics antioxidant defence systems) are crucial which in turn determine fate of cells.

Results: In the present study, we expended TLR expressing (normal/ transformed) and TLR null cells; and we have shown that mannan pretreatment in TLR expressing normal cells offers survival advantage against lethal doses of ionizing radiation. On the contrary, mannan pretreatment does not offer any protection against radiation to TLR null cells, NKE ρ° cells and transformed cells. In normal cells, abrupt decrease in mitochondrial membrane potential and endogenous ROS levels occurs following treatment with mannan. We intend to irradiate mannan-pretreated cells at a specific stage of perturbed mitochondrial functioning and ROS levels to comprehend if mannan pretreatment offers any survival advantage against radiation exposure to cells. Interestingly, pre-irradiation treatment of cells with mannan activates NFκB, p38 and JNK, alters mitochondrial physiology, increases expression of Cu/ZnSOD and MnSOD, minimizes oxidation of mitochondrial phospholipids and offers survival advantage in comparison to irradiated group, in TLR expressing normal cells.

Conclusion: The study demonstrates that TLR and mitochondrial ETC functions are inevitable in radio-protective efficacy exhibited by mannan.

Keywords: Mannan oligosaccharide; Mitochondria; Mitochondrial membrane potential; NFκB; ROS; Radiation protection; TLRs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carbocyanines
  • Cell Line
  • Colony-Forming Units Assay
  • Electron Transport / drug effects
  • Epithelial Cells / drug effects
  • Epithelial Cells / metabolism*
  • Epithelial Cells / radiation effects
  • Genes, Reporter
  • Humans
  • JNK Mitogen-Activated Protein Kinases / metabolism
  • Kinetics
  • Mannans / pharmacology*
  • Membrane Potential, Mitochondrial / drug effects
  • Mitochondria / drug effects
  • Mitochondria / metabolism
  • Mitochondrial Membranes / drug effects
  • Mitochondrial Membranes / metabolism
  • Models, Biological
  • NF-kappa B / metabolism
  • Oligosaccharides / pharmacology*
  • Oxidation-Reduction
  • Phospholipids / metabolism
  • Phosphorylation / drug effects
  • Radiation Protection*
  • Radiation, Ionizing
  • Reactive Oxygen Species / metabolism
  • Superoxide Dismutase / metabolism
  • Time Factors
  • Toll-Like Receptors / metabolism*
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Carbocyanines
  • Mannans
  • NF-kappa B
  • Oligosaccharides
  • Phospholipids
  • Reactive Oxygen Species
  • Toll-Like Receptors
  • 3,3'-dihexyl-2,2'-oxacarbocyanine
  • Superoxide Dismutase
  • JNK Mitogen-Activated Protein Kinases
  • p38 Mitogen-Activated Protein Kinases