Curculigoside Ameliorates Bone Loss by Influencing Mesenchymal Stem Cell Fate in Aging Mice

Senile osteoporosis is characterized by increased bone loss and fat accumulation in marrow. Curculigoside (CCG) is the major bioactive component of Curculigo orchioides, which has been used as anti-osteoporosis therapy for elder patients since antiquity. We aimed to investigate the underlying mechan...

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Autores principales: Na Wang, Ziyi Li, Shilun Li, Yukun Li, Liu Gao, Xiaoxue Bao, Ke Wang, Chang Liu, Peng Xue, Sijing Liu
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Publicado: Frontiers Media S.A. 2021
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Acceso en línea:https://doaj.org/article/50b98c70a6c24a97b66e3aced27c1629
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spelling oai:doaj.org-article:50b98c70a6c24a97b66e3aced27c16292021-12-03T06:19:02ZCurculigoside Ameliorates Bone Loss by Influencing Mesenchymal Stem Cell Fate in Aging Mice2296-634X10.3389/fcell.2021.767006https://doaj.org/article/50b98c70a6c24a97b66e3aced27c16292021-12-01T00:00:00Zhttps://www.frontiersin.org/articles/10.3389/fcell.2021.767006/fullhttps://doaj.org/toc/2296-634XSenile osteoporosis is characterized by increased bone loss and fat accumulation in marrow. Curculigoside (CCG) is the major bioactive component of Curculigo orchioides, which has been used as anti-osteoporosis therapy for elder patients since antiquity. We aimed to investigate the underlying mechanisms by which CCG regulated the bone-fat balance in marrow of aging mice. In our study, CCG treatment was identified to interfere with the stem cell lineage commitment both in vivo and in vitro. In vivo, CCG promoted the transcriptional co-activator with PDZ-binding motif (TAZ) expression to reverse age-related bone loss and marrow adiposity. In vitro, proper concentration of CCG upregulated TAZ expression to increase osteogenesis and decrease adipogenesis of bone marrow mesenchymal stem cells (BMSCs). This regulating effect was discounted by TAZ knockdown or the use of MEK-ERK pathway inhibitor, UO126. Above all, our study confirmed the rescuing effects of CCG on the differential shift from adipogenesis to osteogenesis of BMSCs in aging mice and provided a scientific basis for the clinical use of CCG in senile osteoporosis.Na WangNa WangZiyi LiZiyi LiShilun LiYukun LiYukun LiLiu GaoLiu GaoXiaoxue BaoXiaoxue BaoKe WangKe WangChang LiuChang LiuPeng XuePeng XueSijing LiuFrontiers Media S.A.articleosteoporosiscurculigosideBMSCsTAZMEK-ERK pathwayBiology (General)QH301-705.5ENFrontiers in Cell and Developmental Biology, Vol 9 (2021)
institution DOAJ
collection DOAJ
language EN
topic osteoporosis
curculigoside
BMSCs
TAZ
MEK-ERK pathway
Biology (General)
QH301-705.5
spellingShingle osteoporosis
curculigoside
BMSCs
TAZ
MEK-ERK pathway
Biology (General)
QH301-705.5
Na Wang
Na Wang
Ziyi Li
Ziyi Li
Shilun Li
Yukun Li
Yukun Li
Liu Gao
Liu Gao
Xiaoxue Bao
Xiaoxue Bao
Ke Wang
Ke Wang
Chang Liu
Chang Liu
Peng Xue
Peng Xue
Sijing Liu
Curculigoside Ameliorates Bone Loss by Influencing Mesenchymal Stem Cell Fate in Aging Mice
description Senile osteoporosis is characterized by increased bone loss and fat accumulation in marrow. Curculigoside (CCG) is the major bioactive component of Curculigo orchioides, which has been used as anti-osteoporosis therapy for elder patients since antiquity. We aimed to investigate the underlying mechanisms by which CCG regulated the bone-fat balance in marrow of aging mice. In our study, CCG treatment was identified to interfere with the stem cell lineage commitment both in vivo and in vitro. In vivo, CCG promoted the transcriptional co-activator with PDZ-binding motif (TAZ) expression to reverse age-related bone loss and marrow adiposity. In vitro, proper concentration of CCG upregulated TAZ expression to increase osteogenesis and decrease adipogenesis of bone marrow mesenchymal stem cells (BMSCs). This regulating effect was discounted by TAZ knockdown or the use of MEK-ERK pathway inhibitor, UO126. Above all, our study confirmed the rescuing effects of CCG on the differential shift from adipogenesis to osteogenesis of BMSCs in aging mice and provided a scientific basis for the clinical use of CCG in senile osteoporosis.
format article
author Na Wang
Na Wang
Ziyi Li
Ziyi Li
Shilun Li
Yukun Li
Yukun Li
Liu Gao
Liu Gao
Xiaoxue Bao
Xiaoxue Bao
Ke Wang
Ke Wang
Chang Liu
Chang Liu
Peng Xue
Peng Xue
Sijing Liu
author_facet Na Wang
Na Wang
Ziyi Li
Ziyi Li
Shilun Li
Yukun Li
Yukun Li
Liu Gao
Liu Gao
Xiaoxue Bao
Xiaoxue Bao
Ke Wang
Ke Wang
Chang Liu
Chang Liu
Peng Xue
Peng Xue
Sijing Liu
author_sort Na Wang
title Curculigoside Ameliorates Bone Loss by Influencing Mesenchymal Stem Cell Fate in Aging Mice
title_short Curculigoside Ameliorates Bone Loss by Influencing Mesenchymal Stem Cell Fate in Aging Mice
title_full Curculigoside Ameliorates Bone Loss by Influencing Mesenchymal Stem Cell Fate in Aging Mice
title_fullStr Curculigoside Ameliorates Bone Loss by Influencing Mesenchymal Stem Cell Fate in Aging Mice
title_full_unstemmed Curculigoside Ameliorates Bone Loss by Influencing Mesenchymal Stem Cell Fate in Aging Mice
title_sort curculigoside ameliorates bone loss by influencing mesenchymal stem cell fate in aging mice
publisher Frontiers Media S.A.
publishDate 2021
url https://doaj.org/article/50b98c70a6c24a97b66e3aced27c1629
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