Glutathione-Allylsulfur Conjugates as Mesenchymal Stem Cells Stimulating Agents for Potential Applications in Tissue Repair

Int J Mol Sci. 2020 Feb 28;21(5):1638. doi: 10.3390/ijms21051638.

Abstract

The endogenous gasotransmitter H2S plays an important role in the central nervous, respiratory and cardiovascular systems. Accordingly, slow-releasing H2S donors are powerful tools for basic studies and innovative pharmaco-therapeutic agents for cardiovascular and neurodegenerative diseases. Nonetheless, the effects of H2S-releasing agents on the growth of stem cells have not been fully investigated. H2S preconditioning can enhance mesenchymal stem cell survival after post-ischaemic myocardial implantation; therefore, stem cell therapy combined with H2S may be relevant in cell-based therapy for regenerative medicine. Here, we studied the effects of slow-releasing H2S agents on the cell growth and differentiation of cardiac Lin- Sca1+ human mesenchymal stem cells (cMSC) and on normal human dermal fibroblasts (NHDF). In particular, we investigated the effects of water-soluble GSH-garlic conjugates (GSGa) on cMSC compared to other H2S-releasing agents, such as Na2S and GYY4137. GSGa treatment of cMSC and NHDF increased their cell proliferation and migration in a concentration dependent manner with respect to the control. GSGa treatment promoted an upregulation of the expression of proteins involved in oxidative stress protection, cell-cell adhesion and commitment to differentiation. These results highlight the effects of H2S-natural donors as biochemical factors that promote MSC homing, increasing their safety profile and efficacy after transplantation, and the value of these donors in developing functional 3D-stem cell delivery systems for cardiac muscle tissue repair and regeneration.

Keywords: MSCs; cell differentiation; cell migration; garlic; hydrogen sulfide; organosulfur compounds; oxidative stress; regenerative medicine.

MeSH terms

  • Antioxidants / pharmacology
  • Biomarkers / metabolism
  • Cardiovascular Diseases / genetics
  • Cell Differentiation / drug effects
  • Cell Hypoxia / drug effects
  • Cell Movement / drug effects
  • Cell Plasticity / drug effects
  • Cell Proliferation / drug effects
  • Cell Survival / drug effects
  • Fibroblasts / cytology
  • Fibroblasts / drug effects
  • Gene Expression Regulation / drug effects
  • Glutathione / pharmacology*
  • Humans
  • Hydrogen Sulfide / pharmacology
  • Inactivation, Metabolic / drug effects
  • Mesenchymal Stem Cell Transplantation*
  • Mesenchymal Stem Cells / cytology*
  • Mesenchymal Stem Cells / drug effects
  • Mesenchymal Stem Cells / metabolism
  • Myocardium / cytology
  • Oxidative Stress / drug effects
  • Phenotype
  • Sulfur Compounds / pharmacology*
  • Transcription, Genetic / drug effects
  • Wound Healing / drug effects*

Substances

  • Antioxidants
  • Biomarkers
  • Sulfur Compounds
  • Glutathione
  • Hydrogen Sulfide