The Effect of Co-treating Human Mesenchymal Stem Cells with Epigallocatechin Gallate and Hypoxia-Inducible Factor-1 on the Expression of RANKL/RANK/OPG Signaling Pathway, Osteogenesis, and Angiogenesis Genes
Autor: | Sayyed Mohammad Hossein Ghaderian, Bahar Mohammadi, Mir Davood Omrani, Zahra Fazeli, Zahra Esmaeilizade, Masoumeh Rajabibazl |
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Rok vydání: | 2021 |
Předmět: |
musculoskeletal diseases
biology Angiogenesis Mesenchymal stem cell Biomedical Engineering Medicine (miscellaneous) Cell Biology Epigallocatechin gallate Bone tissue Biomaterials RUNX2 chemistry.chemical_compound medicine.anatomical_structure chemistry Downregulation and upregulation RANKL Cancer research medicine biology.protein Stem cell |
Zdroj: | Regenerative Engineering and Translational Medicine. 8:117-124 |
ISSN: | 2364-4141 2364-4133 |
DOI: | 10.1007/s40883-021-00197-z |
Popis: | Mesenchymal stem cells (MSCs) were considered the promising source in the regeneration of bone tissue. These cells have been known to have the ability to differentiate into the osteogenic lineage. The identification of the new approaches improved the efficiency of these cells in bone tissue engineering. In the present study, we investigated the combinational effect of epigallocatechin gallate (EGCG) and hypoxia-inducible factor-1 (HIF-1) on the osteogenic differentiation ability of human bone marrow-mesenchymal stem cells (BM-MSCs). Ten differently treated groups of BM-MSCs were evaluated by expression analysis of osteogenic and angiogenic markers including Runx2, COL1A1, SPARC, VEGF, and ALP as well as RANKL/RANK/OPG pathway genes. They included the experimental (cells treated with the culture medium containing 5, 10, and 20 μM EGCG with 15, 30, and 45 ng/ml HIF-1 or without HIF-1) and the control groups (untreated cells). The obtained results indicated that the co-treating with 5 μM EGCG+ 30 ng/ml HIF-1 increased the osteogenic ability of BM-MSCs as compared with the other experimental groups and the control cells. Furthermore, treatment with EGCG and HIF-1 showed to be associated with the RANKL upregulation as well as OPG downregulation. These observations suggested that HIF-1 improved the EGCG efficiency in the MSC differentiation into the osteogenic lineage. The administration of mesenchymal stem cells (MSCs) has been suggested to be a potential therapy tool in the repair of bone tissue. The identification of novel approaches could play an important role in the improvement of bone tissue engineering. In the present study, we investigated the effect of co-treating the human MSCs with epigallocatechin gallate (EGCG) and hypoxia-inducible factor-1 (HIF-1). The obtained results provided the better understanding about the effect of EGCG and HIF-1 on expression level of Runx2, COL1A1, SPARC, VEGF, ALP, OPG, and RANKL genes in the treated cells. |
Databáze: | OpenAIRE |
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