Searchable abstracts of presentations at key conferences on calcified tissues
Bone Abstracts (2014) 3 PP169 | DOI: 10.1530/boneabs.3.PP169

Cell biology: osteoclasts and bone resorption

Mechanosensitive TRP channels are required for Ca2+ signaling in osteoclastogenesis

Yu-Mi Yang, Jiae Lee & Dong Min Shin

9 views


Department of Oral Biology, BK21 PLUS Project, Yonsei University College of Dentistry, Seoul, Republic of Korea.


Bone remodeling and maintenance require a fine balance between bone formation of osteoblasts and resorption of osteoclasts. Therefore, various skeletal disorders cause by imbalanced differentiation and activities of these cells. RANKL (receptor activator of NF-kB ligand) induces Ca2+ oscillations and activates NFATc1 (nuclear factor of activated T cells i) during osteoclast differentiation. Although Ca2+ oscillations play a key role for osteoclastogenesis, the molecular identification of Ca2+ influx via mechanosensitive calcium channels located on the plasma membrane for the generation of Ca2+ oscillation are not well known. We investigated the expression and functional role of mechanosensitive TRP (transient receptor potential) channels on Ca2+ signaling during osteoclastogenesis in RAW264.7 and bone marrow macrophage (BMM) cells. Ca2+ oscillations and entry were changed by the over-expression of TRPC3 and TRPC6. Activation of these channels had effects on the expression of NFATc1, activation of ERK pathway, and regulation of osteoclast differentiation. These results suggest that mechanosensitive TRP channels play a key role in the Ca2+ signaling of osteoclastogenesis. This research was supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, Science and Technology (MEST) (2012R1A1A2007673).

Volume 3

European Calcified Tissue Society Congress 2014

Prague, Czech Republic
17 May 2014 - 20 May 2014

European Calcified Tissue Society 

Browse other volumes

Article tools

My recent searches

No recent searches.

My recently viewed abstracts

No recent abstracts.