[Frontiers in Bioscience 16, 2598-2621, June 1, 2011]

Biomineralization of bone: a fresh view of the roles of non-collagenous proteins

Jeffrey Paul Gorski1

1Center of Excellence in the Study of Musculoskeletal and Dental Tissues and Dept. of Oral Biology, Sch. Of Dentistry, Univ. of Missouri-Kansas City, Kansas City, MO 64108

TABLE OF CONTENTS

1. Abstract
2. Introduction
3. Proposed mechanisms of mineral nucleation in bone
3.1. Biomineralization Foci
3.2. Calcospherulites
3.3. Matrix vesicles
4. The role of individual non-collagenous proteins
4.1. Bone Sialoprotein
4.2. Noggin
4.3. Chordin
4.4. Osteopontin
4.5. Osteopontin, bone sialoprotein, and DMP1 form individual complexes with MMPs
4.6. Bone acidic glycoprotein-75
4.7. Dentin matrix protein1
4.8. Osteocalcin
4.9. Fetuin (alpha2HS-glycoprotein)
4.10. Periostin
4.11. Tissue nonspecific alkaline phosphatase
4.12. Phospho 1 phosphatase
4.13. Ectonucleotide pyrophosphatase/phosphodiesterase
4.14. Biological effects of hydroxyapatite on bone matrix proteins
4.15. Sclerostin
4.16. Tenascin C
4.17. Phosphate-regulating neutral endopeptidase (PHEX)
4.18. Matrix extracellular phosphoglycoprotein (MEPE, OF45)
4.19. Functional importance of proteolysis in activation of transglutaminase and PCOLCE
4.20. Neutral proteases in bone
5. Summary and Perspective
6. Acknowledgements
7. References

1. ABSTRACT

The impact of genetics has dramatically affected our understanding of the functions of non-collagenous proteins. Specifically, mutations and knockouts have defined their cellular spectrum of actions. However, the biochemical mechanisms mediated by non-collagenous proteins in biomineralization remain elusive. It is likely that this understanding will require more focused functional testing at the protein, cell, and tissue level. Although initially viewed as rather redundant and static acidic calcium binding proteins, it is now clear that non-collagenous proteins in mineralizing tissues represent diverse entities capable of forming multiple protein-protein interactions which act in positive and negative ways to regulate the process of bone mineralization. Several new examples from the author's laboratory are provided which illustrate this theme including an apparent activating effect of hydroxyapatite crystals on metalloproteinases. This review emphasizes the view that secreted non-collagenous proteins in mineralizing bone actively participate in the mineralization process and ultimately control where and how much mineral crystal is deposited, as well as determining the quality and biomechanical properties of the mineralized matrix produced.