Zn(II)-Chlorido complexes of phytohormone kinetin and its derivatives modulate expression of inflammatory mediators in THP-1 cells

PLoS One. 2013 Jun 3;8(6):e65214. doi: 10.1371/journal.pone.0065214. Print 2013.

Abstract

Kinetin (N6-furfuryladenine) belongs to a group of plant growth hormones involved in cell division, differentiation and other physiological processes. One of the possible ways to obtain biologically active compounds is to complex biologically relevant natural compounds to suitable metal atoms. In this work, two structural groups of Zn(II) complexes [Zn(L(n))2Cl2]·Solv (1-5) and [Zn(HL(n))Cl3] · xL(n) (6-7); n=1-5, Solv=CH3OH for 1 and 2H2O for 2; x =1 for 6 and 2 for 7; involving a phytohormone kinetin and its derivatives (L(n)) were evaluated for their ability to modulate secretion of tumour necrosis factor (TNF)-α, interleukin (IL)-1β and matrix metalloproteinase (MMP)-2 in a lipopolysaccharide (LPS)-activated macrophage-like THP-1 cell model. The penetration of the complexes to cells was also detected. The mechanism of interactions of the zinc(II) complexes with a fluorescent sensor N-(6-methoxy-8-quinolyl)-p-toluene sulphonamide (TSQ) and sulfur-containing biomolecules (l-cysteine and reduced glutathione) was studied by electrospray-ionization mass spectrometry and flow-injection analysis with fluorescence detection. The present study showed that the tested complexes exhibited a low cytotoxic effect on the THP-1 cell line (IC50>40 µM), apart from complex 4, with an IC50=10.9 ± 1.1 µM. Regarding the inflammation-related processes, the Zn(II) complexes significantly decreased IL-1β production by a factor of 1.47-2.22 compared with the control (DMSO), but did not affect TNF-α and MMP-2 secretions. However, application of the Zn(II) complexes noticeably changed the pro-MMP-2/MMP-2 ratio towards a higher amount of maturated MMP-2, when they induced a 4-times higher production of maturated MMP-2 in comparison with the vehicle-treated cells under LPS stimulation. These results indicated that the complexes are able to modulate an inflammatory response by influencing secretion and activity of several inflammation-related cytokines and enzymes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aminoquinolines
  • Anti-Inflammatory Agents / chemical synthesis
  • Anti-Inflammatory Agents / pharmacology*
  • Biological Transport
  • Cations, Divalent
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Chlorides / chemistry
  • Coordination Complexes / chemical synthesis
  • Coordination Complexes / pharmacology*
  • Cysteine / chemistry
  • Fluorescent Dyes
  • Gene Expression / drug effects*
  • Glutathione / chemistry
  • Humans
  • Interleukin-1beta / antagonists & inhibitors
  • Interleukin-1beta / genetics
  • Interleukin-1beta / metabolism
  • Kinetin / chemistry*
  • Lipopolysaccharides / pharmacology
  • Macrophage Activation / drug effects
  • Macrophages / cytology
  • Macrophages / drug effects*
  • Macrophages / metabolism
  • Matrix Metalloproteinase 2 / genetics
  • Matrix Metalloproteinase 2 / metabolism
  • Tosyl Compounds
  • Tumor Necrosis Factor-alpha / genetics
  • Tumor Necrosis Factor-alpha / metabolism
  • Zinc / chemistry*

Substances

  • Aminoquinolines
  • Anti-Inflammatory Agents
  • Cations, Divalent
  • Chlorides
  • Coordination Complexes
  • Fluorescent Dyes
  • Interleukin-1beta
  • Lipopolysaccharides
  • Tosyl Compounds
  • Tumor Necrosis Factor-alpha
  • N-(6-methoxy-8-quinolyl)-4-toluenesulfonamide
  • Matrix Metalloproteinase 2
  • Glutathione
  • Zinc
  • Cysteine
  • Kinetin

Grants and funding

The authors would like to thank the Operational Program Research and Development for Innovations – European Regional Development Fund (CZ.1.05/2.1.00/03.0058), the Operational Program Education for Competitiveness – European Social Fund (CZ.1.07/2.3.00/20.0017) and Palacký University (IGA PrF_2013_015) for financial support. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.