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Effect of idebenone on bone marrow mesenchymal stem cells in vitro.
Zhang, Jiahui; Zhang, Jun; Li, Tao; Zhang, Nannan; Tang, Shengnan; Tao, Zehua; Zhou, Xiaohe; Sun, Xiaochun; Chen, Huabiao.
Afiliação
  • Zhang J; School of Medicine, Jiangsu University, Zhenjiang, Jiangsu 212001, P.R. China.
  • Zhang J; Clinical Laboratory, The Affiliated Hospital of Yangzhou University, Yangzhou, Jiangsu 225001, P.R. China.
  • Li T; School of Medicine, Jiangsu University, Zhenjiang, Jiangsu 212001, P.R. China.
  • Zhang N; School of Medicine, Jiangsu University, Zhenjiang, Jiangsu 212001, P.R. China.
  • Tang S; School of Medicine, Jiangsu University, Zhenjiang, Jiangsu 212001, P.R. China.
  • Tao Z; School of Medicine, Jiangsu University, Zhenjiang, Jiangsu 212001, P.R. China.
  • Zhou X; School of Medicine, Jiangsu University, Zhenjiang, Jiangsu 212001, P.R. China.
  • Sun X; School of Medicine, Jiangsu University, Zhenjiang, Jiangsu 212001, P.R. China.
  • Chen H; School of Medicine, Jiangsu University, Zhenjiang, Jiangsu 212001, P.R. China.
Mol Med Rep ; 17(4): 5376-5383, 2018 04.
Article em En | MEDLINE | ID: mdl-29393352
ABSTRACT
In recent years, stem cell research has continued to benefit from its crossover with chemistry, particularly the investigation of small molecular drugs modulating specific targets to regulate stem cell fate. Idebenone (IDB) is a yellow crystalline powder that is used in the treatment of chronic cerebrovascular diseases. The objective of the present study was to examine whether IDB had an influence on bone marrow­derived mesenchymal stem cells (BMSCs) extracted from the bone marrow of Sprague­Dawley rats. The effects of IDB on cell proliferation, cell cloning and migration were investigated. Cell cycle, apoptosis, DAPI nuclear staining and senescence­associated ß­galactosidase (SA­ß­gal) staining were also examined. The results revealed that IDB at suitable concentrations enhanced cell cloning capacity, promoted the proliferation of BMSCs, delayed cellular senescence, and inhibited cell apoptosis and migration. Western blot analysis indicated that IDB increased the expression of B­cell lymphoma 2 (Bcl­2), signal transducer and activator of transcription­3, Nanog, octamer­binding transcription factor 4, E­cadherin, proliferating cell nuclear antigen, cyclinD1 and cyclinD3, and decreased the expression of Bcl­2­associated X protein, cleaved caspase­3, N­cadherin, vimentin and α­smooth muscle actin. In conclusion, these experiments confirmed that IDB in low doses had no toxic effect and may exert protective effects on BMSCs.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ubiquinona / Células-Tronco Mesenquimais Limite: Animals Idioma: En Revista: Mol Med Rep Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ubiquinona / Células-Tronco Mesenquimais Limite: Animals Idioma: En Revista: Mol Med Rep Ano de publicação: 2018 Tipo de documento: Article