Phenotype disruption of umbilical cord derived MSC by cyclic mechanical stretch and hyperoxia mediated by p21

Preclinical studies provided convincing evidence that umbilical cord derived mesenchymal stem cells (UC-MSC) prevent lung injury and promote lung regeneration. We hypothesized that cyclic mechanical stretch (CMS) and hyperoxia (HOX) during mechanical ventilation account for their limited therapeutic efficacy within the clinics. UC-MSC cultures were subjected to CMS and HOX and evaluated for proliferation, cell viability and further functional properties. Reversibility of the phenotype changes was evaluated after recovery in room air following these exposures. CMS and HOX compromised cell viability and proliferation, altered phenotypic characteristics, particularly PDGFR

  • Goetz, M. J.
  • Behnke, J.
  • Oehmke, F.
  • Holzfurtner, L.
  • Korte, P.
  • Rivetti, S.
  • Bellusci, S.
  • Ehrhardt, H.

Keywords

  • Humans
  • *Mesenchymal Stem Cells/metabolism/cytology
  • *Umbilical Cord/cytology
  • *Hyperoxia/metabolism
  • Phenotype
  • Cell Survival
  • *Cyclin-Dependent Kinase Inhibitor p21/metabolism
  • Cell Proliferation
  • *Stress, Mechanical
  • Cells, Cultured
  • Cellular Senescence
  • Hyperoxia
  • Lung disease
  • Mechanical ventilation
  • Mesenchymal stem cells
  • Senescence
  • p21
Publication details
DOI: 10.1038/s41598-025-22330-6
Journal: Sci Rep
Pages: 35031
Number: 1
Work Type: Original
Access number: 41057469
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