Abstract |
Many bone diseases such as osteoporosis and periodontitis are caused by hyperactivation of osteoclasts. Calcium (Ca2+ ) signals are crucial for osteoclast differentiation and function. Thus, the blockade of Ca2+ signaling may be a strategy for regulating osteoclast activity and has clinical implications. Flunarizine (FN) is a Ca2+ channel antagonist that has been used for reducing migraines. However, the role of FN in osteoclast differentiation and function remains unknown. Here, we investigated whether FN regulates osteoclastogenesis and elucidated the molecular mechanism. FN inhibited osteoclast differentiation along with decreased expression of nuclear factor of activated T cells, cytoplasmic 1 (NFATc1), and attenuated osteoclast maturation and bone resorption. FN inhibition of osteoclast differentiation was restored by ectopic expression of constitutively active NFATc1. FN reduced calcium oscillations and its inhibition of osteoclast differentiation and resorption function was reversed by ionomycin, an ionophore that binds Ca2+ . FN also inhibited Ca2+ / calmodulin-dependent protein kinase IV (CaMKIV) and calcineurin leading to a decrease in the cAMP-responsive element- binding protein-dependent cFos and peroxisome proliferator-activated receptor-γ coactivator 1β expression, and NFATc1 nuclear translocation. These results indicate that FN inhibits osteoclastogenesis via regulating CaMKIV and calcineurin as a Ca2+ channel blocker. In addition, FN-induced apoptosis in osteoclasts and promoted osteogenesis. Furthermore, FN protected lipopolysaccharide- and ovariectomy-induced bone destruction in mouse models, suggesting that it has therapeutic potential for treating inflammatory bone diseases and postmenopausal osteoporosis.
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Authors | Hyun Jin Kim, Jiae Lee, Gong-Rak Lee, Narae Kim, Hye In Lee, Minjeong Kwon, Nam Young Kim, Jin Ha Park, Ye Hee Kang, Hyeong Ju Song, TaeSoo Kim, Dong Min Shin, Woojin Jeong |
Journal | Journal of cellular physiology
(J Cell Physiol)
Vol. 236
Issue 12
Pg. 8239-8252
(12 2021)
ISSN: 1097-4652 [Electronic] United States |
PMID | 34192358
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2021 Wiley Periodicals LLC. |
Chemical References |
- NFATC Transcription Factors
- RANK Ligand
- Calcineurin
- Flunarizine
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Topics |
- Animals
- Bone Resorption
(drug therapy, metabolism)
- Calcineurin
(metabolism)
- Calcium Signaling
(drug effects)
- Cell Differentiation
(drug effects)
- Flunarizine
(antagonists & inhibitors, metabolism)
- Humans
- NFATC Transcription Factors
(drug effects, metabolism)
- Osteoclasts
(drug effects, metabolism)
- Osteogenesis
(drug effects, physiology)
- Osteoporosis
(drug therapy, metabolism)
- RANK Ligand
(metabolism)
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