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This article is part of the supplement: Proceedings of the 8th Global Arthritis Research Network (GARN) Meeting and 1st Bio-Rheumatology International Congress (BRIC)

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Maintenance of mitochondrial DNA copy number is essential for osteoclast survival

Tsuyoshi Miyazaki1*, Shuuichi Mori1, Kazuhiro Shigemoto1, Nils-Goran Larsson2, Takeshi Nakamura3, Shigekaki Kato3, Tomoki Nakashima4, Hiroshi Takayanagi4 and Sakae Tanaka5

  • * Corresponding author: Tsuyoshi Miyazaki

Author Affiliations

1 Department of Geriatric Medicine, Tokyo Metropolitan Geriatric Hospital and Institute of Gerontology, Tokyo 173-0015, Japan

2 Division of Metabolic Diseases, Karolinska Institute, Stockholm, Sweden

3 Institute of Molecular and Cellular Biosciences, The University of Tokyo, Tokyo 113-0032, Japan

4 Department of Cell Signaling, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo 113-8549, Japan

5 Department of Orthopaedic Surgery, Faculty of Medicine, The University of Tokyo, Tokyo 113-0033, Japan

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Arthritis Research & Therapy 2012, 14(Suppl 1):P49  doi:10.1186/ar3650

The electronic version of this article is the complete one and can be found online at:

Published:9 February 2012

© 2012 Miyazaki et al.; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


There is accumulating evidence that osteoclasts, the primary cells responsible for bone resorption, are involved in bone and joint destruction in rheumatoid arthritis. Bone resorption is highly regulated by mature osteoclast function as well as osteoclastogenesis. The life span of mature osteoclasts is relatively short both in vitro and in vivo, and once differentiated, they rapidly die in the absence of supporting cell or growth factors. Mitochondria is known as powerhouse of cell because they generate most of the cell's supply of adenosine triphosphate (ATP), used as a source of chemical energy. In addition to supplying cellular energy, mitochondria are involved in a range of other processes, such as signaling, cellular differentiation, cell growth, and cell death. Transcription and replication of mitochondrial DNA (mtDNA) are important steps in mitochondrial biogenesis and mitochondrial transcription factor A (Tfam) is essential for mtDNA transcription and replication. However, the functional significance of mitochondria has not been established in osteoclastic bone resorption.

Materials and methods

To address this question, we generated osteoclast-specific Tfam conditional knock-out (cKO) mice by mating Tfamfl/fl mice with cathepsin K-Cre transgenic mice, in which the Cre recombinase gene is knocked into the cathepsin K locus and specifically expressed in mature osteoclasts. The in vivo effects of Tfam deficiency on bone metabolism were examined by histological and histomorphometric analysis. The survival and bone-resorbing activity of Tfam cKO osteoclasts were determined by in vitro survival assay and pit formation assay, respectively.


The expression level of Tfam, mtDNA copy number, and cellular ATP level were markedly reduced in osteoclasts derived from Tfam cKO mice. The body size of Tfam cKO mice was smaller than that of the control mice, although trabecular bone volume remained unchanged by Tfam deficiency. However, histological sections of proximal tibia and lumbar spine of Tfam cKO mice showed significantly decreased osteoclast number. Interestingly, Tfam cKO osteoclasts exhibited increased bone-resorbing activity in spite of their pro-apoptotic tendency.


This study demonstrates that Tfam cKO osteoclasts exhibited increased bone resorption with accelerated apoptosis, indicating that there may be an inverse correlation between osteoclast survival vs bone resorption. Further investigation of mitochondria in bone-resorbing osteoclasts will give us new insights into the molecular mechanism regulating bone homeostasis.