Epigallocatechin-3-gallate Protects against Hydrogen Peroxide-Induced Inhibition of Osteogenic Differentiation of Human Bone Marrow-Derived Mesenchymal Stem Cells

Oxidative stress induces bone loss and osteoporosis, and epigallocatechin-3-gallate (EGCG) may be used to combat these diseases due to its antioxidative property. Herein, oxidative stress in human bone marrow-derived mesenchymal stem cells (BM-MSCs) was induced by H2O2, resulting in an adverse effec...

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Main Authors: Dawei Wang, Yonghui Wang, Shihong Xu, Fu Wang, Bomin Wang, Ke Han, Daqing Sun, Lianxin Li
Format: Article
Language:English
Published: Wiley 2016-01-01
Series:Stem Cells International
Online Access:http://dx.doi.org/10.1155/2016/7532798
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author Dawei Wang
Yonghui Wang
Shihong Xu
Fu Wang
Bomin Wang
Ke Han
Daqing Sun
Lianxin Li
author_facet Dawei Wang
Yonghui Wang
Shihong Xu
Fu Wang
Bomin Wang
Ke Han
Daqing Sun
Lianxin Li
author_sort Dawei Wang
collection DOAJ
description Oxidative stress induces bone loss and osteoporosis, and epigallocatechin-3-gallate (EGCG) may be used to combat these diseases due to its antioxidative property. Herein, oxidative stress in human bone marrow-derived mesenchymal stem cells (BM-MSCs) was induced by H2O2, resulting in an adverse effect on their osteogenic differentiation. However, this H2O2-induced adverse effect was nullified when the cells were treated with EGCG. In addition, treatment of BM-MSCs with EGCG alone also resulted in the enhancement of osteogenic differentiation of BM-MSCs. After EGCG treatment, expressions of β-catenin and cyclin D1 were upregulated, suggesting that the Wnt pathway was involved in the effects of EGCG on the osteogenic differentiation of BM-MSCs. This was also confirmed by the fact that the Wnt pathway inhibitor, Dickkopf-1 (DKK-1), can nullify the EGCG-induced enhancement effect on BM-MSC’s osteogenic differentiation. Hence, our results suggested that EGCG can reduce the effects of oxidative stress on Wnt pathway in osteogenic cells, which supported a potentially promising therapy of bone disorders induced by oxidative stress. Considering its positive effects on BM-MSCs, EGCG may also be beneficial for stem cell-based bone repair.
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institution Kabale University
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language English
publishDate 2016-01-01
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series Stem Cells International
spelling doaj-art-f8ddc0104d0e40538e7060fc558284102025-02-03T01:11:18ZengWileyStem Cells International1687-966X1687-96782016-01-01201610.1155/2016/75327987532798Epigallocatechin-3-gallate Protects against Hydrogen Peroxide-Induced Inhibition of Osteogenic Differentiation of Human Bone Marrow-Derived Mesenchymal Stem CellsDawei Wang0Yonghui Wang1Shihong Xu2Fu Wang3Bomin Wang4Ke Han5Daqing Sun6Lianxin Li7Department of Orthopedics, Shandong Provincial Hospital Affiliated to Shandong University, Jinan 250021, ChinaDepartment of Orthopedics, Shandong Provincial Hospital Affiliated to Shandong University, Jinan 250021, ChinaDepartment of Orthopedics, Shandong Provincial Hospital Affiliated to Shandong University, Jinan 250021, ChinaDepartment of Orthopedics, Shandong Provincial Hospital Affiliated to Shandong University, Jinan 250021, ChinaDepartment of Orthopedics, Shandong Provincial Hospital Affiliated to Shandong University, Jinan 250021, ChinaDepartment of Orthopedics, Shandong Provincial Hospital Affiliated to Shandong University, Jinan 250021, ChinaDepartment of Vascular Surgery, Second Hospital of Shandong University, Jinan 250000, ChinaDepartment of Orthopedics, Shandong Provincial Hospital Affiliated to Shandong University, Jinan 250021, ChinaOxidative stress induces bone loss and osteoporosis, and epigallocatechin-3-gallate (EGCG) may be used to combat these diseases due to its antioxidative property. Herein, oxidative stress in human bone marrow-derived mesenchymal stem cells (BM-MSCs) was induced by H2O2, resulting in an adverse effect on their osteogenic differentiation. However, this H2O2-induced adverse effect was nullified when the cells were treated with EGCG. In addition, treatment of BM-MSCs with EGCG alone also resulted in the enhancement of osteogenic differentiation of BM-MSCs. After EGCG treatment, expressions of β-catenin and cyclin D1 were upregulated, suggesting that the Wnt pathway was involved in the effects of EGCG on the osteogenic differentiation of BM-MSCs. This was also confirmed by the fact that the Wnt pathway inhibitor, Dickkopf-1 (DKK-1), can nullify the EGCG-induced enhancement effect on BM-MSC’s osteogenic differentiation. Hence, our results suggested that EGCG can reduce the effects of oxidative stress on Wnt pathway in osteogenic cells, which supported a potentially promising therapy of bone disorders induced by oxidative stress. Considering its positive effects on BM-MSCs, EGCG may also be beneficial for stem cell-based bone repair.http://dx.doi.org/10.1155/2016/7532798
spellingShingle Dawei Wang
Yonghui Wang
Shihong Xu
Fu Wang
Bomin Wang
Ke Han
Daqing Sun
Lianxin Li
Epigallocatechin-3-gallate Protects against Hydrogen Peroxide-Induced Inhibition of Osteogenic Differentiation of Human Bone Marrow-Derived Mesenchymal Stem Cells
Stem Cells International
title Epigallocatechin-3-gallate Protects against Hydrogen Peroxide-Induced Inhibition of Osteogenic Differentiation of Human Bone Marrow-Derived Mesenchymal Stem Cells
title_full Epigallocatechin-3-gallate Protects against Hydrogen Peroxide-Induced Inhibition of Osteogenic Differentiation of Human Bone Marrow-Derived Mesenchymal Stem Cells
title_fullStr Epigallocatechin-3-gallate Protects against Hydrogen Peroxide-Induced Inhibition of Osteogenic Differentiation of Human Bone Marrow-Derived Mesenchymal Stem Cells
title_full_unstemmed Epigallocatechin-3-gallate Protects against Hydrogen Peroxide-Induced Inhibition of Osteogenic Differentiation of Human Bone Marrow-Derived Mesenchymal Stem Cells
title_short Epigallocatechin-3-gallate Protects against Hydrogen Peroxide-Induced Inhibition of Osteogenic Differentiation of Human Bone Marrow-Derived Mesenchymal Stem Cells
title_sort epigallocatechin 3 gallate protects against hydrogen peroxide induced inhibition of osteogenic differentiation of human bone marrow derived mesenchymal stem cells
url http://dx.doi.org/10.1155/2016/7532798
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