Asiaticoside, a component of Centella asiatica attenuates RANKL-induced osteoclastogenesis via NFATc1 and NF-κB signaling pathways.
Animals
Calcium Signaling
Centella
/ chemistry
Extracellular Signal-Regulated MAP Kinases
/ metabolism
Gene Expression Regulation
Macrophages
/ drug effects
Mice
Mice, Inbred C57BL
NF-kappa B
/ metabolism
NFATC Transcription Factors
/ genetics
Osteoclasts
/ drug effects
Osteogenesis
/ drug effects
Phosphorylation
Proto-Oncogene Proteins c-fos
/ metabolism
RANK Ligand
/ pharmacology
RAW 264.7 Cells
Triterpenes
/ isolation & purification
NF-κB
NFAT pathway
RANKL
asiaticoside
osteoclast
Journal
Journal of cellular physiology
ISSN: 1097-4652
Titre abrégé: J Cell Physiol
Pays: United States
ID NLM: 0050222
Informations de publication
Date de publication:
04 2019
04 2019
Historique:
received:
16
12
2017
accepted:
17
07
2018
pubmed:
28
8
2018
medline:
17
3
2020
entrez:
28
8
2018
Statut:
ppublish
Résumé
Identification of natural compounds that inhibit osteoclastogenesis will facilitate the development of antiresorptive treatment of osteolytic bone diseases. Asiaticoside is a triterpenoid derivative isolated from Centella asiatica, which exhibits varying biological effects like angiogenesis, anti-inflammation, wound healing, and osteogenic differentiation. However, its role in osteoclastogenesis remains unknown. Here, we show that Asiaticoside can suppress RANKL-induced osteoclast formation and bone resorption in a dose-dependent manner. Asiaticoside attenuated the expression of osteoclast marker genes including Ctsk, Atp6v0d2, Nfatc1, Acp5, and Dc-stamp. Furthermore, Asiaticoside inhibited RANKL-mediated NF-κB and NFATc1 activities, and RANKL-induced calcium oscillation. Collectively, this study demonstrates that Asiaticoside inhibited osteoclast formation and function through attenuating RANKL-induced key signaling pathways, which may indicate that Asiaticoside is a potential antiresorptive agent against osteoclast-related osteolytic bone diseases.
Substances chimiques
NF-kappa B
0
NFATC Transcription Factors
0
Nfatc1 protein, mouse
0
Proto-Oncogene Proteins c-fos
0
RANK Ligand
0
Triterpenes
0
Extracellular Signal-Regulated MAP Kinases
EC 2.7.11.24
asiaticoside
PKO39VY215
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
4267-4276Informations de copyright
© 2018 Wiley Periodicals, Inc.