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Endocrinology Vol. 140, No. 3 1192-1199
Copyright © 1999 by The Endocrine Society


ARTICLES

1,25-(OH)2D3 Down-Regulates Expression of Phex, a Marker of the Mature Osteoblast1

Brigitte Ecarot and Marguerite Desbarats

Genetics Unit, Shriners Hospital, Departments of Surgery and Human Genetics, McGill University, Montréal, Québec H3G 1A6, Canada

Address all correspondence and requests for reprints to: B. Ecarot, Genetics Unit, Shriners Hospital for Children, 1529 Cedar Avenue, Montréal, Québec H3G 1A6, Canada. E-mail: becarot{at}shriners.mcgill.ca

Mutations in the PHEX/Phex gene, which encodes for a protein with homology to neutral endopeptidases, are responsible for human and murine X-linked hypophosphatemia. The present study examined Phex messenger RNA (mRNA) and protein expression in cultured osteoblasts and its regulation by 1,25-(OH)2D3. Phex mRNA levels were quantitated on Northern blots by densitometric analysis relatively to GAPDH mRNA levels. Immunoreactive Phex protein levels were evaluated by immunoprecipitation using a polyclonal rabbit antiserum raised against a mouse Phex carboxy-terminal peptide.

ß-Glycerophosphate-induced matrix mineralization in primary osteoblast cultures was associated with significant increases in Phex mRNA and protein. Phex mRNA and protein levels were low or undetectable in proliferating preosteoblastic MC3T3-E1 cells and dramatically increased concomitantly with initiation of matrix mineralization. The pattern of Phex expression, however, was similar in nonmineralizing cultures grown in the absence of ß-glycerophosphate, indicating that the induction of Phex expression in MC3T3-E1 cells was related to cell differentiation rather than matrix mineralization. 1,25-(OH)2D3 inhibited mineral deposition and down-regulated Phex mRNA and protein expression in a time- and dose-dependent manner.

These results indicate that Phex is a marker of the fully differentiated osteoblast and that its expression is stimulated during ß-glycerophosphate-induced mineralization in primary osteoblast cultures and down-regulated by 1,25-(OH)2D3, an inhibitor of matrix mineralization. These findings add support for Phex having an important role in bone mineralization.




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