File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1021/jf202015t
- Scopus: eid_2-s2.0-80053103834
- PMID: 21877759
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Pro-bone and antifat effects of green tea and its polyphenol, epigallocatechin, in rat mesenchymal stem cells in vitro
Title | Pro-bone and antifat effects of green tea and its polyphenol, epigallocatechin, in rat mesenchymal stem cells in vitro |
---|---|
Authors | |
Keywords | adipogenesis bone metabolism epigallocatechin green tea mesenchymal stem cell osteogenesis |
Issue Date | 2011 |
Citation | Journal of Agricultural and Food Chemistry, 2011, v. 59, n. 18, p. 9870-9876 How to Cite? |
Abstract | Green tea has been demonstrated recently as a potent bone supportive agent. Our previous studies showed that green tea and its polyphenolic constituents can promote bone-forming osteoblast activities and inhibit the bone-resorpting osteoclast formation. The objective of the present study was to investigate whether green tea and its components can regulate the osteogenic and adipogenic differentiation in pluripotent rat mesenchymal stem cells (MSCs). The rat MSCs were isolated from the bone marrow of tibiae and femora. The cells were treated with decaffeinated green tea extract (GTE) and six tea polyphenols under osteogenic induction. The alkaline phosphatase (ALP) activities and matrix calcium (Ca) deposition were assessed after 7 and 14 days of treatment. Our results demonstrated that GTE could significantly increase ALP dose dependently in the concentrations without cytotoxicity (0-100 μg/mL). Among six tested tea polyphenols, epigallocatechin (EGC) was shown to be the most effective in promoting osteogenic differentiation. At 20 μM, EGC increased ALP levels and Ca deposition significantly by 2.3- and 1.7-fold, respectively, when compared with the control group. EGC also increased the mRNA expression of bone formation markers runt-related transcription factor 2, ALP, osteonectin, and osteopontin. Furthermore, EGC demonstrated its antiadipogenicity by decreasing the adipocyte formation and inhibiting the mRNA expression levels of the adipogenic markers peroxisome proliferator-activated receptor γ, ccaat/enhancer-binding protein β, and fatty acid binding protein 4. In conclusion, this is the first report of the dual action of green tea polyphenol EGC in promoting osteogenesis and inhibiting adipocyte formation in MSCs. Our results provide scientific evidence to support the potential use of green tea in supporting the bone against degenerative diseases such as osteoporosis. © 2011 American Chemical Society. |
Persistent Identifier | http://hdl.handle.net/10722/343077 |
ISSN | 2023 Impact Factor: 5.7 2023 SCImago Journal Rankings: 1.114 |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Ko, Chun Hay | - |
dc.contributor.author | Siu, Wing Sum | - |
dc.contributor.author | Wong, Hing Lok | - |
dc.contributor.author | Shum, Wai Ting | - |
dc.contributor.author | Fung, Kwok Pui | - |
dc.contributor.author | Lau, Clara Bik San | - |
dc.contributor.author | Leung, Ping Chung | - |
dc.date.accessioned | 2024-05-10T09:05:15Z | - |
dc.date.available | 2024-05-10T09:05:15Z | - |
dc.date.issued | 2011 | - |
dc.identifier.citation | Journal of Agricultural and Food Chemistry, 2011, v. 59, n. 18, p. 9870-9876 | - |
dc.identifier.issn | 0021-8561 | - |
dc.identifier.uri | http://hdl.handle.net/10722/343077 | - |
dc.description.abstract | Green tea has been demonstrated recently as a potent bone supportive agent. Our previous studies showed that green tea and its polyphenolic constituents can promote bone-forming osteoblast activities and inhibit the bone-resorpting osteoclast formation. The objective of the present study was to investigate whether green tea and its components can regulate the osteogenic and adipogenic differentiation in pluripotent rat mesenchymal stem cells (MSCs). The rat MSCs were isolated from the bone marrow of tibiae and femora. The cells were treated with decaffeinated green tea extract (GTE) and six tea polyphenols under osteogenic induction. The alkaline phosphatase (ALP) activities and matrix calcium (Ca) deposition were assessed after 7 and 14 days of treatment. Our results demonstrated that GTE could significantly increase ALP dose dependently in the concentrations without cytotoxicity (0-100 μg/mL). Among six tested tea polyphenols, epigallocatechin (EGC) was shown to be the most effective in promoting osteogenic differentiation. At 20 μM, EGC increased ALP levels and Ca deposition significantly by 2.3- and 1.7-fold, respectively, when compared with the control group. EGC also increased the mRNA expression of bone formation markers runt-related transcription factor 2, ALP, osteonectin, and osteopontin. Furthermore, EGC demonstrated its antiadipogenicity by decreasing the adipocyte formation and inhibiting the mRNA expression levels of the adipogenic markers peroxisome proliferator-activated receptor γ, ccaat/enhancer-binding protein β, and fatty acid binding protein 4. In conclusion, this is the first report of the dual action of green tea polyphenol EGC in promoting osteogenesis and inhibiting adipocyte formation in MSCs. Our results provide scientific evidence to support the potential use of green tea in supporting the bone against degenerative diseases such as osteoporosis. © 2011 American Chemical Society. | - |
dc.language | eng | - |
dc.relation.ispartof | Journal of Agricultural and Food Chemistry | - |
dc.subject | adipogenesis | - |
dc.subject | bone metabolism | - |
dc.subject | epigallocatechin | - |
dc.subject | green tea | - |
dc.subject | mesenchymal stem cell | - |
dc.subject | osteogenesis | - |
dc.title | Pro-bone and antifat effects of green tea and its polyphenol, epigallocatechin, in rat mesenchymal stem cells in vitro | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1021/jf202015t | - |
dc.identifier.pmid | 21877759 | - |
dc.identifier.scopus | eid_2-s2.0-80053103834 | - |
dc.identifier.volume | 59 | - |
dc.identifier.issue | 18 | - |
dc.identifier.spage | 9870 | - |
dc.identifier.epage | 9876 | - |
dc.identifier.eissn | 1520-5118 | - |