RRC ID 62546
Author Kao CL, Tai LK, Chiou SH, Chen YJ, Lee KH, Chou SJ, Chang YL, Chang CM, Chen SJ, Ku HH, Li HY.
Title Resveratrol promotes osteogenic differentiation and protects against dexamethasone damage in murine induced pluripotent stem cells.
Journal Stem Cells Dev
Abstract Resveratrol is a natural polyphenol antioxidant that has been shown to facilitate osteogenic differentiation. A recent breakthrough has demonstrated that ectopic expression of four genes is sufficient to reprogram murine and human fibroblasts into induced pluripotent stem (iPS) cells. However, the roles of resveratrol in the differentiation and cytoprotection of iPS cells have never been studied. In this study, we showed that, in addition to cardiac cells, neuron-like cells, and adipocytes, mouse iPS cells could differentiate into osteocyte-like cells. Using atomic force microscopy that provided nanoscale resolution, we monitored mechanical properties of living iPS cells during osteogenic differentiation. The intensity of mineralization and stiffness in differentiating iPS significantly increased after 14 days of osteogenic induction. Furthermore, resveratrol was found to facilitate osteogenic differentiation in both iPS and embryonic stem cells, as shown by increased mineralization, up-regulation of osteogenic markers, and decreased elastic modulus. Dexamethasone-induced apoptosis in iPS cell-derived osteocyte-like cells was effectively prevented by pretreatment with resveratrol. Furthermore, resveratrol significantly increased manganese superoxide dismutase expression and intracellular glutathione level, thereby efficiently decreasing dexamethasone-induced reactive oxygen species (ROS) production and cytotoxicity. Transplantation experiments using iPS cell-derived osteocyte-like cells further demonstrated that oral intake of resveratrol could up-regulate osteopontin expression and inhibit teratoma formation in vivo. In sum, resveratrol can facilitate differentiation of iPS cells into osteocyte-like cells, protect these iPS cell-derived osteocyte-like cells from glucocorticoid-induced oxidative damage, and decrease tumorigenicity of iPS cells. These findings implicate roles of resveratrol and iPS cells in the stem cell therapy of orthopedic diseases.
Volume 19(2)
Pages 247-58
Published 2010-2-1
DOI 10.1089/scd.2009.0186
PMID 19656070
MeSH Animals Anti-Inflammatory Agents, Non-Steroidal / pharmacology Blotting, Western Cell Differentiation / drug effects* Cell Line Cell Survival / drug effects Cell Transplantation / methods Cells, Cultured Dexamethasone / toxicity* Embryonic Stem Cells / cytology Embryonic Stem Cells / metabolism Glucocorticoids / toxicity Green Fluorescent Proteins / genetics Green Fluorescent Proteins / metabolism Induced Pluripotent Stem Cells / cytology* Induced Pluripotent Stem Cells / metabolism Induced Pluripotent Stem Cells / transplantation Lentivirus / genetics Mice Mice, Nude Multipotent Stem Cells / cytology Multipotent Stem Cells / metabolism Octamer Transcription Factor-3 / genetics Octamer Transcription Factor-3 / metabolism Osteocytes / cytology* Osteocytes / metabolism Resveratrol Reverse Transcriptase Polymerase Chain Reaction Stilbenes / pharmacology* Transduction, Genetic
IF 3.153
Resource
Human and Animal Cells Murine germ line-competent iPS cells