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Gamma radiation induces senescence in human adult mesenchymal stem cells from bone marrow and periodontal ligaments
J. Cmielova, R. Havelek, T. Soukup, A. Jiroutová, B. Visek, J. Suchánek, J. Vavrova, J. Mokry, D. Muthna, L. Bruckova, S. Filip, D. English, M. Rezacova
Language English Country England, Great Britain
Document type Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Enzyme Activation radiation effects MeSH
- Apoptosis radiation effects MeSH
- Bone Marrow Cells cytology MeSH
- Adult Stem Cells cytology metabolism radiation effects MeSH
- DNA Breaks, Double-Stranded radiation effects MeSH
- Phosphorylation radiation effects MeSH
- Histones metabolism MeSH
- Cyclin-Dependent Kinase Inhibitor p16 metabolism MeSH
- Cyclin-Dependent Kinase Inhibitor p21 metabolism MeSH
- Caspases metabolism MeSH
- Cell Cycle Checkpoints radiation effects MeSH
- Humans MeSH
- Mesenchymal Stem Cells cytology metabolism radiation effects MeSH
- Tumor Suppressor Protein p53 metabolism MeSH
- Periodontal Ligament cytology MeSH
- Cell Proliferation radiation effects MeSH
- Gene Expression Regulation radiation effects MeSH
- Cellular Senescence radiation effects MeSH
- Cell Survival radiation effects MeSH
- Gamma Rays adverse effects MeSH
- Check Tag
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
PURPOSE: Mesenchymal stem cells isolated from bone marrow (BM-MSC) and periodontal ligament (PLSC) are cells with high proliferative potential and ability to self-renewal. Characterization of these cells under genotoxic stress conditions contributes to the assessment of their prospective usage. The aim of our study was to evaluate changes in BM-MSC and PLSC caused by ionizing radiation. METHODS: Human BM-MSC and PLSC were irradiated with the doses up to 20 Gy by Co(60) and observed 13 days; viability, proliferation, apoptosis and senescence induction, and changes in expression and phosphorylation status of related proteins were studied. RESULTS: Irradiation with the doses up to 20 Gy significantly reduces proliferation, but has no significant effect on cell viability. The activation of tumor suppressor protein 53 (p53) and its phosphorylations on serines 15 and 392 were detected from the first day after irradiation by 20 Gy and remained elevated to day 13. Expression of cyclin-dependent kinases inhibitor 1A (p21(Cip1/Waf1)) increased. The cell cycle was arrested in G2 phase. Instead of apoptosis we have detected hallmarks of stress-induced premature senescence: increase in cyclin-dependent kinases inhibitor 2A (p16(INK4a)) and increased activity of senescence-associated β-galactosidase. CONCLUSION: Mesenchymal stem cells isolated from bone marrow and periodontal ligament respond to ionizing radiation by induction of stress-induced premature senescence without apparent differences in their radiation response.
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- $a Ćmielová, Jana $7 xx0144661 $u Department of Medical Biochemistry, Faculty of Medicine in Hradec Kralove, Charles University, Prague.
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- $a PURPOSE: Mesenchymal stem cells isolated from bone marrow (BM-MSC) and periodontal ligament (PLSC) are cells with high proliferative potential and ability to self-renewal. Characterization of these cells under genotoxic stress conditions contributes to the assessment of their prospective usage. The aim of our study was to evaluate changes in BM-MSC and PLSC caused by ionizing radiation. METHODS: Human BM-MSC and PLSC were irradiated with the doses up to 20 Gy by Co(60) and observed 13 days; viability, proliferation, apoptosis and senescence induction, and changes in expression and phosphorylation status of related proteins were studied. RESULTS: Irradiation with the doses up to 20 Gy significantly reduces proliferation, but has no significant effect on cell viability. The activation of tumor suppressor protein 53 (p53) and its phosphorylations on serines 15 and 392 were detected from the first day after irradiation by 20 Gy and remained elevated to day 13. Expression of cyclin-dependent kinases inhibitor 1A (p21(Cip1/Waf1)) increased. The cell cycle was arrested in G2 phase. Instead of apoptosis we have detected hallmarks of stress-induced premature senescence: increase in cyclin-dependent kinases inhibitor 2A (p16(INK4a)) and increased activity of senescence-associated β-galactosidase. CONCLUSION: Mesenchymal stem cells isolated from bone marrow and periodontal ligament respond to ionizing radiation by induction of stress-induced premature senescence without apparent differences in their radiation response.
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