The Korean Journal of Physiology and Pharmacology

The Korean Society of Pharmacology (대한약리학회)
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TRPM7 Is Essential for RANKL-Induced Osteoclastogenesis

  • Yang, Yu-Mi (Department of Oral Biology, Yonsei University College of Dentistry) ;
  • Jung, Hwi-Hoon (Department of Pediatric Dentistry, Yonsei University College of Dentistry) ;
  • Lee, Sung Jun (Department of Oral Biology, Yonsei University College of Dentistry) ;
  • Choi, Hyung-Jun (Department of Pediatric Dentistry, Yonsei University College of Dentistry) ;
  • Kim, Min Seuk (Department of Oral Physiology, College of Dentistry, Wonkwang University) ;
  • Shin, Dong Min (Department of Oral Biology, Yonsei University College of Dentistry)
  • Received : 2012.10.31
  • Accepted : 2013.01.20
  • Published : 2013.02.28
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Abstract

The transient receptor potential melastatin type 7 (TRPM7) channel is a widely expressed non-selective cation channel with fusion to the C-terminal alpha kinase domain and regarded as a key regulator of whole body $Mg^{2+}$ homeostasis in mammals. However, the roles of TRPM7 during osteoclastogenesis in RAW264.7 cells and bone marrow-derived monocyte/macrophage precursor cells (BMMs) are not clear. In the present study, we investigate the roles of TRPM7 in osteoclastogenesis using methods of small interfering RNA (siRNA), RT-PCR, patch-clamp, and calcium imaging. RANKL (receptor activator of NF-${\kappa}B$ ligand) stimulation did not affect the TRPM7 expression and TRPM7-mediated current was activated in HEK293, RAW264.7, and BMM cells by the regulation of $Mg^{2+}$. Knock-down of TRPM7 by siTRPM7 reduced intracellular $Ca^{2+}$ concentration ($[Ca^{2+}]_i$) increases by 0 mM $[Mg^{2+}]_e$ in HEK293 cells and inhibited the generation of RANKL-induced $Ca^{2+}$ oscillations in RAW264.7 cells. Finally, knock-down of TRPM7 suppressed RANKL-mediated osteoclastogenesis such as activation and translocation of NFATc1, formation of multinucleated cells, and the bone resorptive activity, sequentially. These results suggest that TRPM7 plays an essential role in the RANKL-induced $[Ca^{2+}]_i$ oscillations that triggers the late stages of osteoclastogenesis.

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References

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