The properties of chitosan complexes with smooth and rough forms of lipopolysaccharides on CHO-K1 cells

Carbohydr Polym. 2013 Sep 12;97(2):284-92. doi: 10.1016/j.carbpol.2013.05.008. Epub 2013 May 14.

Abstract

The negative charge of LPS molecule and the presence of fatty acids in lipid A structure make it capable of binding with chitosan. In the presented work we analyzed the interactions of chitosan with LPS of Burkholderia cepacia or Proteus mirabilis and biological effects of these complexes on CHO-K1 cells. We observed that the presence of O-polysaccharide part of LPS (S1959), core region (R110) or lack of fatty acids in lipid A increased binding affinity of endotoxin with chitosan. However, lipid A of B. cepacia or P. mirabilis R45 might interact with CHO-K1 cells membrane alone or mediated by chitosan, respectively. In conclusion, the presence of two (B. cepacia) or one (P. mirabilis R45) Ara4N residues in lipid A part, promoted binding to cell membrane of CHO-K1 cells, alone or in the presence of chitosan, respectively. Chitosan reduced biological potencies of P. mirabilis lipid A R45 structure and this effect depended on the presence of O-PS. Lipid A of B. cepacia induced oxidative DNA damage in CHO-K1 cells.

Keywords: Bulkhorderia; CHO-K1 cells; Chitosan; Comet assay; Lipopolysaccharide; Proteus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Burkholderia / chemistry
  • CHO Cells
  • Chemical Precipitation
  • Chitosan / pharmacology*
  • Colistin / metabolism
  • Complement Activation / drug effects
  • Cricetinae
  • Cricetulus
  • DNA Damage
  • Enzyme-Linked Immunosorbent Assay
  • Humans
  • Kinetics
  • Lipopolysaccharides / chemistry*
  • Lipopolysaccharides / pharmacology*
  • Mutagens / toxicity
  • Proteus mirabilis / chemistry

Substances

  • Lipopolysaccharides
  • Mutagens
  • Chitosan
  • Colistin