Abstract

Mesenchymal stromal cells (MSCs) are not a homogenous population but comprehend several cell types, such as stem cells, progenitor cells, fibroblasts, and other types of cells. Among these is a population of pluripotent stem cells, which represent around 1–3% of MSCs. These cells, named multilineage-differentiating stress enduring (Muse) cells, are stress-tolerant cells.Stem cells may undergo several rounds of intrinsic and extrinsic stresses due to their long life and must have a robust and effective DNA damage checkpoint and DNA repair mechanism, which, following a genotoxic episode, promote the complete recovery of cells rather than triggering senescence and/or apoptosis.We evaluated how Muse cells can cope with DNA damaging stress in comparison with MSCs. We found that Muse cells were resistant to chemical and physical genotoxic stresses better than non-Muse cells. Indeed, the level of senescence and apoptosis was lower in Muse cells. Our results proved that the DNA damage repair system (DDR) was properly activated following injury in Muse cells. While in non-Muse cells some anomalies may have occurred because, in some cases, the activation of the DDR persisted by 48 hr post damage, in others no activation took place.In Muse cells, the non-homologous end joining (NHEJ) enzymatic activity increases compared to other cells, while single-strand repair activity (NER, BER) does not. In conclusion, the high ability of Muse cells to cope with genotoxic stress is related to their quick and efficient sensing of DNA damage and activation of DNA repair systems.

Highlights

  • Mesenchymal stromal cells (MSCs) are present in the stroma of several organs and tissues, such as bone marrow, adipose tissue, dental pulp, and umbilical cord

  • We evaluated the level of apoptosis and senescence following chemical and physical genotoxic stress, that is, peroxide hydrogen (H2O2) treatment and UV irradiation, respectively

  • We evaluated apoptosis 1 and 48 hr post-treatment, whereas senescence was determined only at 48 hr

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Summary

Introduction

Mesenchymal stromal cells (MSCs) are present in the stroma of several organs and tissues, such as bone marrow, adipose tissue, dental pulp, and umbilical cord. Stem cells present in an MSC population can differentiate into mesodermal lineage cells (adipocytes, chondrocytes, osteocytes, and muscle cells) and in cells belonging to endodermal and ectodermal lineages, www.oncotarget.com at least in vitro [2]. For this reason, several researchers proposed that MSCs may contain a subpopulation of pluripotent stem cells. Muse cells express the pluripotent surface marker SSEA-3 and other pluripotency genes (NANOG, OCT-3/4, SOX2). They can differentiate into triploblastic cells from a single cell and are self-renewable [2, 3]

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