Tmem64 Modulates Calcium Signaling during RANKL-Mediated Osteoclast Differentiation

SummaryOsteoclast maturation and function primarily depend on receptor activator of NF-κB ligand (RANKL)-mediated induction of nuclear factor of activated T cells c1 (NFATc1), which is further activated via increased intracellular calcium ([Ca2+]i) oscillation. However, the coordination mechanism that mediates Ca2+ oscillation during osteoclastogenesis remains ill defined. Here, we identified transmembrane protein 64 (Tmem64) as a regulator of Ca2+ oscillation during osteoclastogenesis. We found that Tmem64-deficient mice exhibit increased bone mass due in part to impaired osteoclast formation. Using in vitro osteoclast culture systems, we show here that Tmem64 interacts with sarcoplasmic endoplasmic reticulum Ca2+ ATPase 2 (SERCA2) and modulates its activity. Consequently, Tmem64 deficiency significantly diminishes RANKL-induced [Ca2+]i oscillation, which results in reduced Ca2+/calmodulin-dependent protein kinases (CaMK) IV and mitochondrial ROS, both of which contribute to achieving the CREB activity necessary for osteoclast formation. These data demonstrate that Tmem64 is a positive modulator of osteoclast differentiation via SERCA2-dependent Ca2+ signaling.

Graphical AbstractFigure optionsDownload high-quality image (171 K)Download as PowerPoint slideHighlights
► Tmem64-deficient mice show increased bone volume
► Tmem64 deficiency reduces [Ca2+]i oscillation in response to RANKL stimulation
► Tmem64 interacts with SERCA2
► Tmem64 positively regulates osteoclast formation via SERCA2/Ca2+ signaling