Aucubin Impeded Preosteoclast Fusion and Enhanced CD31hi EMCNhi Vessel Angiogenesis in Ovariectomized Mice

Osteogenesis is tightly correlated with angiogenesis during the process of bone development, regeneration, and remodeling. In addition to providing nutrients and oxygen for bone tissue, blood vessels around bone tissue also secrete some factors to regulate bone formation. Type H vessels which were r...

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Main Authors: Ziyi Li, Chang Liu, Xiaoli Liu, Na Wang, Liu Gao, Xiaoxue Bao, Sijing Liu, Peng Xue
Format: Article
Language:English
Published: Hindawi Limited 2022-01-01
Series:Stem Cells International
Online Access:http://dx.doi.org/10.1155/2022/5226771
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author Ziyi Li
Chang Liu
Xiaoli Liu
Na Wang
Liu Gao
Xiaoxue Bao
Sijing Liu
Peng Xue
author_facet Ziyi Li
Chang Liu
Xiaoli Liu
Na Wang
Liu Gao
Xiaoxue Bao
Sijing Liu
Peng Xue
author_sort Ziyi Li
collection DOAJ
description Osteogenesis is tightly correlated with angiogenesis during the process of bone development, regeneration, and remodeling. In addition to providing nutrients and oxygen for bone tissue, blood vessels around bone tissue also secrete some factors to regulate bone formation. Type H vessels which were regulated by platelet-derived growth factor-BB (PDGF-BB) were confirmed to couple angiogenesis and osteogenesis. Recently, preosteoclasts have been identified as the most important source of PDGF-BB. Therefore, inhibiting osteoclast maturation, improving PDGF-BB secretion, stimulating type H angiogenesis, and subsequently accelerating bone regeneration may be potent treatments for bone loss disease. In the present study, aucubin, an iridoid glycoside extracted from Aucuba japonica and Eucommia ulmoides, was found to inhibit bone loss in ovariectomized mice. We further confirmed that aucubin could inhibit the fusion of tartrate-resistant acid phosphatase (TRAP)+ preosteoclasts into mature osteoclasts and indirectly increasing angiogenesis of type H vessel. The underlying mechanism is the aucubin-induced inhibition of MAPK/NF-κB signaling, which increases the preosteoclast number and subsequently promotes angiogenesis via PDGF-BB. These results prompted that aucubin could be an antiosteoporosis drug candidate, which needs further research.
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spelling doaj.art-30d9189086d342179b834fd838d1301d2022-12-22T04:39:50ZengHindawi LimitedStem Cells International1687-96782022-01-01202210.1155/2022/5226771Aucubin Impeded Preosteoclast Fusion and Enhanced CD31hi EMCNhi Vessel Angiogenesis in Ovariectomized MiceZiyi Li0Chang Liu1Xiaoli Liu2Na Wang3Liu Gao4Xiaoxue Bao5Sijing Liu6Peng Xue7Department of EndocrinologyDepartment of EndocrinologyDepartment of Pediatric DentistryDepartment of EndocrinologyDepartment of EndocrinologyDepartment of EndocrinologyEditorial Department of Hebei Medical UniversityDepartment of EndocrinologyOsteogenesis is tightly correlated with angiogenesis during the process of bone development, regeneration, and remodeling. In addition to providing nutrients and oxygen for bone tissue, blood vessels around bone tissue also secrete some factors to regulate bone formation. Type H vessels which were regulated by platelet-derived growth factor-BB (PDGF-BB) were confirmed to couple angiogenesis and osteogenesis. Recently, preosteoclasts have been identified as the most important source of PDGF-BB. Therefore, inhibiting osteoclast maturation, improving PDGF-BB secretion, stimulating type H angiogenesis, and subsequently accelerating bone regeneration may be potent treatments for bone loss disease. In the present study, aucubin, an iridoid glycoside extracted from Aucuba japonica and Eucommia ulmoides, was found to inhibit bone loss in ovariectomized mice. We further confirmed that aucubin could inhibit the fusion of tartrate-resistant acid phosphatase (TRAP)+ preosteoclasts into mature osteoclasts and indirectly increasing angiogenesis of type H vessel. The underlying mechanism is the aucubin-induced inhibition of MAPK/NF-κB signaling, which increases the preosteoclast number and subsequently promotes angiogenesis via PDGF-BB. These results prompted that aucubin could be an antiosteoporosis drug candidate, which needs further research.http://dx.doi.org/10.1155/2022/5226771
spellingShingle Ziyi Li
Chang Liu
Xiaoli Liu
Na Wang
Liu Gao
Xiaoxue Bao
Sijing Liu
Peng Xue
Aucubin Impeded Preosteoclast Fusion and Enhanced CD31hi EMCNhi Vessel Angiogenesis in Ovariectomized Mice
Stem Cells International
title Aucubin Impeded Preosteoclast Fusion and Enhanced CD31hi EMCNhi Vessel Angiogenesis in Ovariectomized Mice
title_full Aucubin Impeded Preosteoclast Fusion and Enhanced CD31hi EMCNhi Vessel Angiogenesis in Ovariectomized Mice
title_fullStr Aucubin Impeded Preosteoclast Fusion and Enhanced CD31hi EMCNhi Vessel Angiogenesis in Ovariectomized Mice
title_full_unstemmed Aucubin Impeded Preosteoclast Fusion and Enhanced CD31hi EMCNhi Vessel Angiogenesis in Ovariectomized Mice
title_short Aucubin Impeded Preosteoclast Fusion and Enhanced CD31hi EMCNhi Vessel Angiogenesis in Ovariectomized Mice
title_sort aucubin impeded preosteoclast fusion and enhanced cd31hi emcnhi vessel angiogenesis in ovariectomized mice
url http://dx.doi.org/10.1155/2022/5226771
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