Chronic senescent human mesenchymal stem cells as possible contributor to the wound healing disorder after exposure to the alkylating agent sulfur mustard.
Simone RothmillerNiklas JägerNicole MeierThimo MeyerAdrian NeuDirk SteinritzHorst ThiermannMichael SchererChristoph RummelAswin MangerichAlexander BürkleAnnette SchmidtPublished in: Archives of toxicology (2021)
Wound healing is a complex process, and disturbance of even a single mechanism can result in chronic ulcers developing after exposure to the alkylating agent sulfur mustard (SM). A possible contributor may be SM-induced chronic senescent mesenchymal stem cells (MSCs), unable to fulfil their regenerative role, by persisting over long time periods and creating a proinflammatory microenvironment. Here we show that senescence induction in human bone marrow derived MSCs was time- and concentration-dependent, and chronic senescence could be verified 3 weeks after exposure to between 10 and 40 µM SM. Morphological changes, reduced clonogenic and migration potential, longer scratch closure times, differences in senescence, motility and DNA damage response associated genes as well as increased levels of proinflammatory cytokines were revealed. Selective removal of these cells by senolytic drugs, in which ABT-263 showed initial potential in vitro, opens the possibility for an innovative treatment strategy for chronic wounds, but also tumors and age-related diseases.
Keyphrases
- mesenchymal stem cells
- endothelial cells
- wound healing
- umbilical cord
- stem cells
- dna damage response
- dna damage
- bone marrow
- drug induced
- high glucose
- induced apoptosis
- cell therapy
- dna methylation
- transcription factor
- signaling pathway
- dna repair
- induced pluripotent stem cells
- cell death
- cystic fibrosis
- cell proliferation
- staphylococcus aureus
- cell cycle arrest
- pluripotent stem cells
- bioinformatics analysis