The Role of Phosphatases in the Initiation of Skeletal Mineralization

• Published in: Calcified tissue international 2013-10, Vol.93 (4), p.299-306
• Main Author: Millan, Jose Luis
• Format: Article
• Language: English
• Subjects: Alkaline Phosphatase - metabolism; Animals; Biochemistry; Biomedical and Life Sciences; Bone and Bones - embryology; Bone and Bones - metabolism; Calcification, Physiologic - physiology; Carrier Proteins - metabolism; Cartilage; Cell Biology; Chick Embryo; Chondrocytes - cytology; Endocrinology; Extracellular Matrix - metabolism; Humans; Hypophosphatasia - embryology; Life Sciences; Mice; Mice, Transgenic; Mineralization; Original Research; Orthopedics; Osteoblasts - cytology; Phosphates; Phosphoric Diester Hydrolases - metabolism; Phosphoric Monoester Hydrolases - metabolism; Pyrophosphatases - metabolism; Skeletal system
• ISSN: 0171-967X; 1432-0827
• DOI: 10.1007/s00223-012-9672-8

Endochondral ossification is a carefully orchestrated process mediated by promoters and inhibitors of mineralization. Phosphatases are implicated, but their identities and functions remain unclear. Mutations in the tissue-nonspecific alkaline phosphatase (TNAP) gene cause hypophosphatasia, a heritable form of rickets and osteomalacia, caused by an arrest in the propagation of hydroxyapatite (HA) crystals onto the collagenous extracellular matrix due to accumulation of extracellular inorganic pyrophosphate (PP i ), a physiological TNAP substrate and a potent calcification inhibitor. However, TNAP knockout ( Alpl –/– ) mice are born with a mineralized skeleton and have HA crystals in their chondrocyte- and osteoblast-derived matrix vesicles (MVs). We have shown that PHOSPHO1, a soluble phosphatase with specificity for two molecules present in MVs, phosphoethanolamine and phosphocholine, is responsible for initiating HA crystal formation inside MVs and that PHOSPHO1 and TNAP have nonredundant functional roles during endochondral ossification. Double ablation of PHOSPHO1 and TNAP function leads to the complete absence of skeletal mineralization and perinatal lethality, despite normal systemic phosphate and calcium levels. This strongly suggests that the P i needed for initiation of MV-mediated mineralization is produced locally in the perivesicular space. As both TNAP and nucleoside pyrophosphohydrolase-1 (NPP1) behave as potent ATPases and pyrophosphatases in the MV compartment, our current model of the mechanisms of skeletal mineralization implicate intravesicular PHOSPHO1 function and P i influx into MVs in the initiation of mineralization and the functions of TNAP and NPP1 in the extravesicular progression of mineralization.