How to influence the mesenchymal stem cells fate? Emerging role of ectoenzymes metabolizing nucleotides.
Katarzyna RoszekMagdalena WujakPublished in: Journal of cellular physiology (2018)
Extracellular purines, principally adenosine triphosphate and adenosine, are among the oldest evolutionary and widespread chemical messengers. The integrative view of purinergic signaling as a multistage coordinated cascade involves the participation of nucleotides/nucleosides, their receptors, enzymes metabolizing extracellular nucleosides and nucleotides as well as several membrane transporters taking part in the release and/or uptake of these molecules. In view of the emerging data, it is evident and widely accepted that an extensive network of diverse enzymatic activities exists in the extracellular space. The enzymes regulate the availability of nucleotide and adenosine receptor agonists, and consequently, the course of signaling events. The current data indicate that mesenchymal stem cells (MSCs) and cells induced to differentiate exhibit different sensitivity to purinergic ligands as well as a distinct activity and expression profiles of ectonucleotidases than mature cells. In the proposed review, we postulate for a critical role of these enzymatic players which, by orchestrating a fine-tune regulation of nucleotides concentrations, are integrally involved in modulation and diversification of purinergic signals. This specific hallmark of the MSC purinome should be linked with cell-specific biological potential and capacity for tissue regeneration. We anticipate this publication to be a starting point for scientific discussion and novel approach to the in vitro and in vivo regulation of the MSC properties.
Keyphrases
- mesenchymal stem cells
- induced apoptosis
- umbilical cord
- cell cycle arrest
- stem cells
- cell therapy
- electronic health record
- bone marrow
- hydrogen peroxide
- protein kinase
- oxidative stress
- physical activity
- single cell
- signaling pathway
- gene expression
- high glucose
- diabetic rats
- dna methylation
- nitric oxide
- climate change
- pi k akt