Methotrexate released in vitro from bone cement inhibits human stem cell proliferation in S/G2 phase
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
19205701
PubMed Central
PMC2899262
DOI
10.1007/s00264-008-0717-6
Knihovny.cz E-zdroje
- MeSH
- antimetabolity antitumorózní aplikace a dávkování chemie MeSH
- buňky kostní dřeně účinky léků patologie MeSH
- interfáze účinky léků MeSH
- kostní cementy chemie MeSH
- kultivované buňky MeSH
- lidé MeSH
- methotrexát aplikace a dávkování chemie MeSH
- mezenchymální kmenové buňky účinky léků patologie MeSH
- proliferace buněk účinky léků MeSH
- viabilita buněk účinky léků MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antimetabolity antitumorózní MeSH
- kostní cementy MeSH
- methotrexát MeSH
Methotrexate (MTX) released from bone cement showed a useful local effect in animal models of bone tumours. However, local toxic reactions such as impaired wound healing were observed in areas surrounding the MTX-loaded implant. Therefore, we hypothesised that MTX released from bone cement would have harmful effects on human mesenchymal stem cells (MSC)-one of the basic components of bone marrow and tissue reparatory processes. Moreover, elution of MTX was calculated from implants prepared either with liquid or powdered MTX. During the 28-day incubation, the cement compounded with liquid MTX showed the highest elution rate of the drug. MTX released from pellets produced a significant decrease in proliferation of MSC as a consequence of a blockade of their cell cycle in the S/G2 phase. These findings indicate impairment of stem cell function in marginal areas surrounding the MTX-loaded cement and may help to explain problems with regeneration of tissues in these locations.
Le Methotrexate (MTX) libéré par le ciment acrylique a un effet certain sur les tumeurs osseuses développées sur un modèle animal. Cependant, des réactions toxiques locales telles que défauts de cicatrisation ont été observées à proximité de l’implantation de ce ciment. Nous faisons donc l’hypothèse que le Methotrexate MTX libéré par le ciment a un effet nocif néfaste sur les cellules mésenchyméteuses humaines MSC qui sont l’un des composants de base de la moelle osseuse et des phénomènes de la réparation tissulaire. De plus, la dynamique de pénétration du méthotrexate a été analysée à partir d’implants préparés avec du liquide ou de la poudre de méthotrexate. Au cours des 28 jours d’incubation, le ciment préparé avec du méthotrexate liquide montre un taux important de pénétration de la drogue. Le méthotrexate libéré des billes de ciment entraîne une diminution significative de la prolifération des cellules mésenchyméteuses avec un bloquage cellulaire à la phase S/G2. Ces travaux montrent que la fonction cellulaire est altérée au voisInage du méthotrexate pouvant expliquer les problèmes de régénétration tissulaire.
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