Matrix first, minerals later: fine-tuned dietary phosphate increases bone formation in zebrafish
Status PubMed-not-MEDLINE Jazyk angličtina Země Anglie, Velká Británie Médium electronic-ecollection
Typ dokumentu časopisecké články
PubMed
39045128
PubMed Central
PMC11264301
DOI
10.1093/jbmrpl/ziae081
PII: ziae081
Knihovny.cz E-zdroje
- Klíčová slova
- analysis/quantitation of bone, animal models, collagen, matrix mineralization, osteoblasts,
- Publikační typ
- časopisecké články MeSH
Bone matrix formation and mineralization are two closely related, yet separated processes. Matrix formation occurs first, mineralization is a second step strictly dependent on the dietary intake of calcium and phosphorus (P). However, mineralization is commonly used as diagnostic parameter for bone-related diseases. In this context, bone loss, often characterized as a condition with reduced bone mineral density, represents a major burden for human health, for which increased dietary mineral intake is generally recommended. Using a counterintuitive approach, we use a low-P diet followed by a sufficient-P intake to increase bone volume. We show in zebrafish by histology, qPCR, micro-CT, and enzyme histochemistry that a two-months period of reduced dietary P intake stimulates extensive formation of new bone matrix, associated with the upregulation of key genes required for both bone matrix formation and mineralization. The return to a P-sufficient diet initiates the mineralization of the abundant matrix previously deposited, thus resulting in a striking increase of the mineralized bone volume as proven at the level of the vertebral column, including vertebral bodies and arches. In summary, bone matrix formation is first stimulated with a low-P diet, and its mineralization is later triggered by a sufficient-P dietary intake. In zebrafish, the uncoupling of bone formation and mineralization by alternating low and sufficient dietary P intake significantly increases the bone volume without causing skeletal malformations or ectopic mineralization. A modification of this approach to stimulate bone formation, optimized for mammalian models, can possibly open opportunities to support treatments in patients that suffer from low bone mass.
Biology Department Evolutionary Developmental Biology Ghent University 9000 Gent Belgium
Department of Biology University of Rome Tor Vergata 00133 Rome Italy
Department of Molecular Medicine Biochemistry Unit University of Pavia 27100 Pavia Italy
Department of Zoology Charles University 12800 Prague Czech Republic
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