Cargando…

Asperosaponin VI stimulates osteogenic differentiation of rat adipose-derived stem cells

In the aging population, the decrease on osteogenic differentiation resulted into a significant reduction in bone formation. Bone tissue engineering has been a successful technique for treatment of bone defects. It is reported that adipose-derived stem cells (ADSCs) have pluripotency to differentiat...

Descripción completa

Detalles Bibliográficos
Autores principales: Ding, Xingpo, Li, Wuyin, Chen, Dengshan, Zhang, Chuanwei, Wang, Lei, Zhang, Hong, Qin, Na, Sun, Yongqiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japanese Society for Regenerative Medicine 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6518317/
https://www.ncbi.nlm.nih.gov/pubmed/31193169
http://dx.doi.org/10.1016/j.reth.2019.03.007
_version_ 1783418432806453248
author Ding, Xingpo
Li, Wuyin
Chen, Dengshan
Zhang, Chuanwei
Wang, Lei
Zhang, Hong
Qin, Na
Sun, Yongqiang
author_facet Ding, Xingpo
Li, Wuyin
Chen, Dengshan
Zhang, Chuanwei
Wang, Lei
Zhang, Hong
Qin, Na
Sun, Yongqiang
author_sort Ding, Xingpo
collection PubMed
description In the aging population, the decrease on osteogenic differentiation resulted into a significant reduction in bone formation. Bone tissue engineering has been a successful technique for treatment of bone defects. It is reported that adipose-derived stem cells (ADSCs) have pluripotency to differentiate into adipocytes and osteoblasts. However little is revealed about the effect of the herbal medicine Asperosaponin VI (ASA VI) on ADSCs differentiation. In our study, we isolated and identified ADSCs from rats. We examined the effect of different concentrations of ASA VI in ADSCs on alkaline phosphatase (ALP) activity, calcium deposition, the expression of bone-related proteins and the release of inflammatory cytokines. Flowcytometry assay showed ADSCs were highly expressed CD44 and CD105, but hardly expressed CD34 and CD45, suggesting ADSCs were successfully isolated for follow-up experiments. ALP activity examination and Alizarin red (AR) stain showed that ASA VI enhanced the ALP activity and promoted matrix mineralization in ADSCs. In addition, bone-related protein OCN and RUNX2, and Smad2/3 phosphorylation was upregulated after ASA VI treatment in ADSCs. ELISA results showed that ASA VI blocked the release of TNF-α, IL-6 and IL-1β in ADSCs. Considering this results, we concluded that ASA VI promotes osteogenic differentiation of ADSCs through inducing the expression of bone-related proteins. These findings enriched the function of ASA VI as a regenerative medicine and shed new light for the treatment of bone defects in clinical research.
format Online
Article
Text
id pubmed-6518317
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Japanese Society for Regenerative Medicine
record_format MEDLINE/PubMed
spelling pubmed-65183172019-05-21 Asperosaponin VI stimulates osteogenic differentiation of rat adipose-derived stem cells Ding, Xingpo Li, Wuyin Chen, Dengshan Zhang, Chuanwei Wang, Lei Zhang, Hong Qin, Na Sun, Yongqiang Regen Ther Original Article In the aging population, the decrease on osteogenic differentiation resulted into a significant reduction in bone formation. Bone tissue engineering has been a successful technique for treatment of bone defects. It is reported that adipose-derived stem cells (ADSCs) have pluripotency to differentiate into adipocytes and osteoblasts. However little is revealed about the effect of the herbal medicine Asperosaponin VI (ASA VI) on ADSCs differentiation. In our study, we isolated and identified ADSCs from rats. We examined the effect of different concentrations of ASA VI in ADSCs on alkaline phosphatase (ALP) activity, calcium deposition, the expression of bone-related proteins and the release of inflammatory cytokines. Flowcytometry assay showed ADSCs were highly expressed CD44 and CD105, but hardly expressed CD34 and CD45, suggesting ADSCs were successfully isolated for follow-up experiments. ALP activity examination and Alizarin red (AR) stain showed that ASA VI enhanced the ALP activity and promoted matrix mineralization in ADSCs. In addition, bone-related protein OCN and RUNX2, and Smad2/3 phosphorylation was upregulated after ASA VI treatment in ADSCs. ELISA results showed that ASA VI blocked the release of TNF-α, IL-6 and IL-1β in ADSCs. Considering this results, we concluded that ASA VI promotes osteogenic differentiation of ADSCs through inducing the expression of bone-related proteins. These findings enriched the function of ASA VI as a regenerative medicine and shed new light for the treatment of bone defects in clinical research. Japanese Society for Regenerative Medicine 2019-05-10 /pmc/articles/PMC6518317/ /pubmed/31193169 http://dx.doi.org/10.1016/j.reth.2019.03.007 Text en © 2019 The Japanese Society for Regenerative Medicine. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Ding, Xingpo
Li, Wuyin
Chen, Dengshan
Zhang, Chuanwei
Wang, Lei
Zhang, Hong
Qin, Na
Sun, Yongqiang
Asperosaponin VI stimulates osteogenic differentiation of rat adipose-derived stem cells
title Asperosaponin VI stimulates osteogenic differentiation of rat adipose-derived stem cells
title_full Asperosaponin VI stimulates osteogenic differentiation of rat adipose-derived stem cells
title_fullStr Asperosaponin VI stimulates osteogenic differentiation of rat adipose-derived stem cells
title_full_unstemmed Asperosaponin VI stimulates osteogenic differentiation of rat adipose-derived stem cells
title_short Asperosaponin VI stimulates osteogenic differentiation of rat adipose-derived stem cells
title_sort asperosaponin vi stimulates osteogenic differentiation of rat adipose-derived stem cells
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6518317/
https://www.ncbi.nlm.nih.gov/pubmed/31193169
http://dx.doi.org/10.1016/j.reth.2019.03.007
work_keys_str_mv AT dingxingpo asperosaponinvistimulatesosteogenicdifferentiationofratadiposederivedstemcells
AT liwuyin asperosaponinvistimulatesosteogenicdifferentiationofratadiposederivedstemcells
AT chendengshan asperosaponinvistimulatesosteogenicdifferentiationofratadiposederivedstemcells
AT zhangchuanwei asperosaponinvistimulatesosteogenicdifferentiationofratadiposederivedstemcells
AT wanglei asperosaponinvistimulatesosteogenicdifferentiationofratadiposederivedstemcells
AT zhanghong asperosaponinvistimulatesosteogenicdifferentiationofratadiposederivedstemcells
AT qinna asperosaponinvistimulatesosteogenicdifferentiationofratadiposederivedstemcells
AT sunyongqiang asperosaponinvistimulatesosteogenicdifferentiationofratadiposederivedstemcells