Melatonin protects gingival mesenchymal stem cells and promotes differentiation into osteoblasts

被引:6
|
作者
Sola, Veronica M. [1 ,2 ]
Aguilar, Juan J. [3 ,4 ]
Farias, Adrian [3 ]
Vazquez Mosquera, Ana P. [1 ,2 ,4 ]
Peralta Lopez, Maria E. [1 ]
Carpentieri, Agata R. [1 ,2 ]
机构
[1] Univ Nacl Cordoba UNC, Fac Odontol, Catedra Quim Biol B, Pabellon Argentina,Haya La Torre S-N,Ciudad Univ, RA-5000 Cordoba, Argentina
[2] INICSA UNC CONICET, Inst Invest Ciencias Salud, Cordoba, Argentina
[3] UNC, Fac Ciencias Med, Inst Virol Dr Jose Maria Vanella, Cordoba, Argentina
[4] UNC, Catedra Introducc La Fis & Quim Biol B, Fac Odontol, Cordoba, Argentina
关键词
differentiation; melatonin; mesenchymal gingival cells; oxidative stress; periodontitis; PERIODONTAL REGENERATION; STROMAL CELLS; IN-VITRO; OSTEOPENIA;
D O I
10.1002/cbf.3733
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Melatonin (MEL) has antioxidant properties and participates in osteogenic differentiation. In periodontitis, in which increased oxidative stress and bone resorption are involved, mesenchymal stem cells derived from the gingiva (GMSCs) combined with MEL could be relevant for osteogenic regeneration. In this study, we studied the antioxidant and differentiating effect of MEL on an in vitro system of GMSCs. Primary culture of GMSCs from Wistar rats was developed to evaluate differentiation into osteoblasts with an appropriate medium with or without MEL. Marker genes of mesenchymal stem cells by real time-polymerase chain reaction, clonogenic capacity, and cell migration after wound assay were used to characterize GMSCs as mesenchymal stem cells. Alkaline phosphatase activity and the alizarin red technique were used to evaluate osteogenic activity and differentiation. MEL increased alkaline phosphatase activity and alizarin red values, promoting osteogenic differentiation. Besides this, MEL protected GMSCs in a model of cellular damage related to oxidative stress, returning viability to baseline. MEL was more effective in promoting and protecting GMSCs by the production of osteogenic cells when oxidative stress is present. This evidence supports the use of MEL as a novel bone-regenerative therapy in periodontal diseases.
引用
收藏
页码:636 / 646
页数:11
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