- Login
- Register
- Home/Current Issue
- About the journal
- Editorial board
- Online submission
- Instructions for authors
- Subscriptions
- Foundation Acta Endocrinologica
- Archive
- Contact
Romanian Academy
The Publishing House of the Romanian Academy
ACTA ENDOCRINOLOGICA (BUC)
The International Journal of Romanian Society of Endocrinology / Registered in 1938in Web of Science Master Journal List
Acta Endocrinologica(Bucharest) is live in PubMed Central
Journal Impact Factor - click here.
This Article
Services
Google Scholar
PubMed
Acta Endocrinologica (Buc)
Wei S, Liu K, Wu H, Hu J, He J, Li G, Liu B, Yang W
MT2 Inhibits Osteoclastogenesis by Scavenging Ros
Acta Endo (Buc) 2023, 19 (4): 447-455doi: 10.4183/aeb.2023.447
Context and objective. Reactive oxygen species
(ROS) produced under oxidative stress is important for
osteoclastogenesis. As a major member of the metallothionein
(MT) family, metallothionein2 (MT2) can scavenge ROS in
osteoblasts. However, the role of MT2 in osteoclastogenesis
and ROS production in osteoclast precursors (OCPs) is
unknown.
Material and methods. In this study, we first
investigated MT2 expression level in osteoporotic model
mice. Next, we explored the roles of MT2 in osteoclastic
differentiation and ROS production in OCPs. Ultimately,
via rescue assays based on hydrogen peroxide (H2O2),
the significance of ROS in MT-2-regulated osteoclastic
differentiation was further elucidated.
Results. Compared with sham operated (Sham)
mice, ovariectomized (OVX) mice displayed bone marrow
primary OCPs (Ly6C+CD11b-) having higher ROS levels
and lower MT2 expression. MT2 overexpression inhibited
the formation of mature osteoclasts, while MT2 knockdown
was contrary. Moreover, MT2 overexpression inhibited
ROS production in OCPs, while MT2 knockdown exhibited
the opposite effects. Notably, the inhibitory effect of MT2
overexpression on osteoclastogenesis and ROS production
was blocked by the addition of H2O2.
Conclusion. MT2 inhibits osteoclastogenesis
through repressing ROS production in OCPs, which
indicates that the strategy of upregulating MT2 in OCPs may
be applied to the clinical treatment of osteoclastic bone loss.
Keywords: Metallothionein2, Osteoclast, Reactive oxygen species, Hydrogen peroxide, Osteoclastogenesis
Correspondence: Sevcihan GünenYilmaz, Assoc. Prof., Department of Oral and Maxillofacial Radiology, Faculty of Dentistry, Akdeniz
University, Antalya, Turkey, E-mail: dentistsevcihan@hotmail.com