6-Bromoindirubin-3’-oxime promotes osteogenic differentiation of canine BMSCs through inhibition of GSK3β activity and activation of the Wnt/β-catenin signaling pathway

This study aimed to investigate how 6-bromoindirubin-3’-oxime (BIO) increases the osteogenic differentiation of canine bone mesenchymal stem cells (BMSCs) and the role of the Wnt/β-catenin signaling pathway in this process. We mimicked the effect of Wnt by adding BIO to the culture medium of BMSCs a...

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Main Authors: XIAO-E ZHAO, ZHENSHAN YANG, ZHEN GAO, JUNBANG GE, QIANG WEI, BAOHUA MA
Format: Article
Language:English
Published: Academia Brasileira de Ciências 2019-03-01
Series:Anais da Academia Brasileira de Ciências
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0001-37652019000100610&lng=en&tlng=en
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author XIAO-E ZHAO
ZHENSHAN YANG
ZHEN GAO
JUNBANG GE
QIANG WEI
BAOHUA MA
author_facet XIAO-E ZHAO
ZHENSHAN YANG
ZHEN GAO
JUNBANG GE
QIANG WEI
BAOHUA MA
author_sort XIAO-E ZHAO
collection DOAJ
description This study aimed to investigate how 6-bromoindirubin-3’-oxime (BIO) increases the osteogenic differentiation of canine bone mesenchymal stem cells (BMSCs) and the role of the Wnt/β-catenin signaling pathway in this process. We mimicked the effect of Wnt by adding BIO to the culture medium of BMSCs and examined whether canonical Wnt signaling positively affects the differentiation of these cells into osteoblasts. Canine BMSCs were cultured with 0.5 and 1.0 μM BIO under osteogenic conditions and then differentiation markers were investigated. It was found that BIO significantly increased the activity of alkaline phosphatase (ALP), the number of ALP-positive cells, the mineralization level and calcium deposits. Moreover, cells cultured with 0.5 and 1.0 μM BIO exhibited detectable β-catenin expression in their nuclei, and showed upregulated β-catenin and glycogen synthase kinase 3 beta(GSK3β) phosphorylation compared to untreated cells. In addition, BIO enhanced the mRNA expression of osteoblast differentiation markers such as ALP, runt-related transcription factor 2, collagen I, osteocalcin, and osteonectin. In conclusion, BIO upregulated GSK3β phosphorylation and inhibited its activity, thereby activating the Wnt/β-catenin signaling pathway and promoting the osteogenic differentiation of canine BMSCs. The effect of 1.0 μM BIO on BMSCs differentiation was stronger than that of 0.5 μM BIO.
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spelling doaj.art-2c4d8a9d75b941018ec25883056bf7522022-12-21T19:40:32ZengAcademia Brasileira de CiênciasAnais da Academia Brasileira de Ciências1678-26902019-03-0191110.1590/0001-3765201920180459S0001-376520190001006106-Bromoindirubin-3’-oxime promotes osteogenic differentiation of canine BMSCs through inhibition of GSK3β activity and activation of the Wnt/β-catenin signaling pathwayXIAO-E ZHAOZHENSHAN YANGZHEN GAOJUNBANG GEQIANG WEIBAOHUA MAThis study aimed to investigate how 6-bromoindirubin-3’-oxime (BIO) increases the osteogenic differentiation of canine bone mesenchymal stem cells (BMSCs) and the role of the Wnt/β-catenin signaling pathway in this process. We mimicked the effect of Wnt by adding BIO to the culture medium of BMSCs and examined whether canonical Wnt signaling positively affects the differentiation of these cells into osteoblasts. Canine BMSCs were cultured with 0.5 and 1.0 μM BIO under osteogenic conditions and then differentiation markers were investigated. It was found that BIO significantly increased the activity of alkaline phosphatase (ALP), the number of ALP-positive cells, the mineralization level and calcium deposits. Moreover, cells cultured with 0.5 and 1.0 μM BIO exhibited detectable β-catenin expression in their nuclei, and showed upregulated β-catenin and glycogen synthase kinase 3 beta(GSK3β) phosphorylation compared to untreated cells. In addition, BIO enhanced the mRNA expression of osteoblast differentiation markers such as ALP, runt-related transcription factor 2, collagen I, osteocalcin, and osteonectin. In conclusion, BIO upregulated GSK3β phosphorylation and inhibited its activity, thereby activating the Wnt/β-catenin signaling pathway and promoting the osteogenic differentiation of canine BMSCs. The effect of 1.0 μM BIO on BMSCs differentiation was stronger than that of 0.5 μM BIO.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0001-37652019000100610&lng=en&tlng=enBone mesenchymal stem cellsbromoindirubin oximeosteogenetic differentiationcanine
spellingShingle XIAO-E ZHAO
ZHENSHAN YANG
ZHEN GAO
JUNBANG GE
QIANG WEI
BAOHUA MA
6-Bromoindirubin-3’-oxime promotes osteogenic differentiation of canine BMSCs through inhibition of GSK3β activity and activation of the Wnt/β-catenin signaling pathway
Anais da Academia Brasileira de Ciências
Bone mesenchymal stem cells
bromoindirubin oxime
osteogenetic differentiation
canine
title 6-Bromoindirubin-3’-oxime promotes osteogenic differentiation of canine BMSCs through inhibition of GSK3β activity and activation of the Wnt/β-catenin signaling pathway
title_full 6-Bromoindirubin-3’-oxime promotes osteogenic differentiation of canine BMSCs through inhibition of GSK3β activity and activation of the Wnt/β-catenin signaling pathway
title_fullStr 6-Bromoindirubin-3’-oxime promotes osteogenic differentiation of canine BMSCs through inhibition of GSK3β activity and activation of the Wnt/β-catenin signaling pathway
title_full_unstemmed 6-Bromoindirubin-3’-oxime promotes osteogenic differentiation of canine BMSCs through inhibition of GSK3β activity and activation of the Wnt/β-catenin signaling pathway
title_short 6-Bromoindirubin-3’-oxime promotes osteogenic differentiation of canine BMSCs through inhibition of GSK3β activity and activation of the Wnt/β-catenin signaling pathway
title_sort 6 bromoindirubin 3 oxime promotes osteogenic differentiation of canine bmscs through inhibition of gsk3β activity and activation of the wnt β catenin signaling pathway
topic Bone mesenchymal stem cells
bromoindirubin oxime
osteogenetic differentiation
canine
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0001-37652019000100610&lng=en&tlng=en
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