Matrix Mineralization as a Trigger for Osteocyte Maturation

Kazuharu Irie ^1*, Sadakazu Ejiri ¹, Yasunori Sakakura ¹, Toru Shibui ¹ and Toshihiko Yajima ¹

¹ Division of Anatomy, Department of Oral Growth and Development, Health Sciences University of Hokkaido School of Dentistry, Hokkaido, Japan (KI,YS,TS,TY), and Division of Anatomy and Cell Biology of the Hard Tissue, Department of Tissue Regeneration and Reconstruction, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan (SE)

^* To whom correspondence should be addressed. E-mail: irie{at}hoku-iryo-u.ac.jp.

Submitted on December 9, 2007
Accepted on 11 February 2008

	Abstract

The morphology of the osteocyte changes during the cell’s lifetime. Shortly after becoming buried in the matrix, an osteocyte is plump with a rich rough endoplasmic reticulum and a well developed Golgi complex. This "immature" osteocyte reduces its number of organelles to become a "mature" osteocyte when it comes to reside deeper in the bone matrix. We hypothesized that mineralization of the surrounding matrix is the trigger for osteocyte maturation. To verify this, we prevented mineralization of newly formed matrix by administration of 1-hydroxyethylidene-1,1-bisphosphonate (HEBP) and then examined the morphological changes in the osteocytes in rats. In HEBP group, matrix mineralization was disturbed but matrix formation was not affected. The osteocytes found in the unmineralized matrix were immature. Mature osteocytes were seen in the corresponding mineralized matrix in control group. The immature osteocytes in the unmineralized matrix failed to show immunoreactivity with anti-sclerostin antibody, whereas mature osteocytes in the mineralized matrix showed immunoreactivity in both control and HEBP groups. These findings suggest that mineralization of the matrix surrounding the osteocyte is the trigger for cytodifferentiation from a plump immature form to a mature osteocyte. The osteocyte appears to start secreting sclerostin only after it matures in the mineralized bone matrix.

Key Words: bisphosphonate, bone matrix, mineralization, osteocyte, sclerostin/SOST

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