Bone Regeneration Based on Orientation of Biological Apatite (BAp) C-Axis in Osteopetrotic (op/op) Mice

Article Preview

Abstract:

The diagnosis of hard tissues is generally carried out by bone mineral density (BMD) measurement as a bone quantity parameter. BMD, however, does not necessarily explain bone fracture risks in some clinical cases. Recently, various parameters relating to bone strength have been investigated. These additional parameters, so-called bone quality, reflect intrinsic bone conditions. We have been studying the preferential alignment of the biological apatite (BAp) c-axis among various bone quality parameters. BAp, a dominant component of hard tissue, is an ionic crystal that crystallizes in a hexagonal lattice accompanied with the anisotropic property. In this article, we investigated the osteoclast role in the recovery process of BAp orientation during bone regeneration using osteopetrotic (op/op) mice in which the number of osteoclasts decreases. A surgically drilled, 500-μm diameter hole on each tibia of both control and op/op 8-week-old mice was introduced from the medial surface into the medullary cavity located at a 30% length from the proximal tibia end. After surgery, tibiae injuries were regularly observed by in situ micro-CT, and then the mice were sacrificed four to eight weeks after surgery. BAp orientation was analyzed in and near the regenerated portion by the microbeam X-ray diffraction system. As a result, we found the insufficient recovery of BAp orientation in spite of the apparent repair of bone appearance and quantity from CT images, even eight weeks after surgery in both cases of control and op/op mice. We conclude that this defective animal model can be used to evaluate bone quantity and quality at the cortical portion during bone regeneration in gene-defect mice in which the expression of bone cells is controlled, for example.

You might also be interested in these eBooks

Info:

Periodical:

Materials Science Forum (Volumes 638-642)

Pages:

588-593

Citation:

Online since:

January 2010

Export:

Price:

[1] R. Marcus, M. Wong, H. Heath III and J. L. Stock: Endocr. Rev. Vol. 23 (2002), p.16.

Google Scholar

[2] J. F. Veenland, T. M. Link, W. Konermann, N. Meier, J. L. Grashuis, and E. S. Gelsema: Calcif. Tissue Int. Vol. 61 (1997), p.474.

DOI: 10.1007/s002239900370

Google Scholar

[3] T. Nakano, Y. Kaibara, Y. Tabata, N. Nagata, S. Enomoto, E. Marukawa, and Y. Umakoshi: Bone Vol. 31 (2002), p.479.

DOI: 10.1016/s8756-3282(02)00850-5

Google Scholar

[4] T. Ishimoto, T. Nakano, Y. Umakoshi, M. Yamamoto, and Y. Tabata: Mater. Sci. Forum Vol. 561-565 (2006), p.261.

Google Scholar

[5] J.W. Lee, T. Nakano, A. Kobayashi, K. Takaoka, Y. Tabata, and Y. Umakoshi: Phosph. Res. Bull. Vol. 17 (2004), p.83.

Google Scholar

[6] T. Nakano, K. Kaibara, Y. Tabata, N. Nagata, S. Enomoto, E. Marukawa and Y. Umakoshi: Tissue Engineering for Therapeutic Use 6 (Elsevier Science B. V. 2002), p.95.

Google Scholar

[7] J.C. Elliott: Structure and Chemistry of the Apatites and Other Calcium Orthophosphates (Elsevier Science B. V. 1994), p.191.

Google Scholar

[8] K. J. Bundy: Ann. Biomed. Eng. Vol. 13 (1985), p.119.

Google Scholar

[9] K. Hasegawa, C.H. Turner and D.B. Burr: Calcif. Tissue Int. Vol. 55 (1994), p.381.

Google Scholar

[10] S. L. Abboud, K. Woodruff, C. Liu, V. Shen, and N. Ghosh-Choudhury: Endocrinology Vol. 143 (2002), p. (1942).

Google Scholar

[11] H. Ida, T. Noda, H. Shimokawa and T. Saku: J. Oral Pathol. & Med. Vol. 31 (2002), p.361.

Google Scholar

[12] K. Sasaki, T. Nakano, J. D. Ferrara, J. W. Lee and T. Sasaki: Mater. Trans. Vol. 49 (2008), p.2129.

Google Scholar

[13] S. Abe, H. Watanabe, A. Hirayama, E. Shibuya, M. Hashimoto and Y. Ide: B.J.R. Vol. 73 (2000), p.1078.

Google Scholar

[14] G. R. Ryan, X. D. Dai, M. G. Dominguez, W. Tong, F. Chuan, O. Chisholm, R. G. Russell, J. W. Pollard, and E. R. Stanley: Blood Vol. 98 (2001), p.74.

Google Scholar

[15] T. M. Campbell, W. T. Wong and E. J. Mackie: Calcif. Tissue Int. Vol. 73 (2003), p.49.

Google Scholar

[16] S. Chiba, K. Okada, K. Lee, G. V. Segre, and R. M. Neer: J. Vet. Med. Sci. Vol. 63 (2001), p.603.

Google Scholar

[17] N. Sakagami, N. Amizuka, M. Li, K. Takeuchi, M. Hoshino, M. Nakamura, K. Nozawa-Inoue, N. Udagawa and T. Maeda: Micron Vol. 36 (2005), p.688.

DOI: 10.1016/j.micron.2005.06.008

Google Scholar

[18] J. W. Lee, T. Nakano, S. Toyosawa, N. Ijuhin, Y. Tabata, M. Yamaoto, and Y. Umakoshi: Mater. Sci. Forum. Vol. 512 (2006), p.265.

Google Scholar

[19] J. W. Lee, T. Nakano, S. Toyosawa, Y. Tabata and Y. Umakoshi: Mater. Trans. Vol. 48 (2007), p.337.

Google Scholar

[20] J. W. Lee, T. Nakano, S. Toyosawa, Y. Tabata and Y. Umakoshi: Adv. Mater. Res. Vol. 26-28 (2007), p.761.

Google Scholar