Abstract

Extracellular ATP through the activation of the P2X and P2Y purinergic receptors affects the migration, proliferation and differentiation of many types of cells, including stem cells. High plasticity, low immunogenicity and immunomodulation ability of mesenchymal stem cells derived from human endometrium (eMSCs) allow them to be considered a prominent tool for regenerative medicine. Here, we examined the role of ATP in the proliferation and migration of human eMSCs. Using a wound healing assay, we showed that ATP‐induced activation of purinergic receptors suppressed the migration ability of eMSCs. We found the expression of one of the ATP receptors, the P2X7 receptor in eMSCs. In spite of this, cell activation with specific P2X7 receptor agonist, BzATP did not significantly affect the cell migration. The allosteric P2X7 receptor inhibitor, AZ10606120 also did not prevent ATP‐induced inhibition of cell migration, confirming that inhibition occurs without P2X7 receptor involvement. Flow cytometry analysis showed that high concentrations of ATP did not have a cytotoxic effect on eMSCs. At the same time, ATP induced the cell cycle arrest, suppressed the proliferative and migration capacity of eMSCs and therefore could affect the regenerative potential of these cells.

Highlights

  • Mesenchymal stem cells (MSCs) are derived from a wide range of adult tissues, including adipose tissue, cartilage, tendons, tooth pulp and periodontal ligament

  • Our results show that ATP decreases the migration capacity of endometrial stem cells (eMSCs)

  • Experiments have been performed on mesenchymal stem cell line derived from the human endometrium

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Summary

| INTRODUCTION

Mesenchymal stem cells (MSCs) are derived from a wide range of adult tissues, including adipose tissue, cartilage, tendons, tooth pulp and periodontal ligament. The population of endometrial stem cells (eMSCs) was first isolated from endometrial tissue samples and characterized only in 2004.6,7 Later, researchers isolated and characterized stem cells from menstrual blood samples.[8-10]. The capacity of stem cells to migrate to the specific tissues or organs is essential for normal tissue homeostasis, morphogenesis and repair, and for creation of stem cell-based regenerative medicines.[23,24,27,28]. This investigation was designed to explore the impact of extracellular ATP on migration and proliferation capacity of endometrial stem cells. Our results demonstrate that the cultivation of cells in the presence of ATP potently suppresses cells growth by inducing accumulation of eMSCs in G0/G1 phase

| MATERIALS AND METHODS
Findings
| DISCUSSION
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