Increased PHOSPHO1 and alkaline phosphatase expression during the anabolic bone response to intermittent parathyroid hormone delivery.


Journal

Cell biochemistry and function
ISSN: 1099-0844
Titre abrégé: Cell Biochem Funct
Pays: England
ID NLM: 8305874

Informations de publication

Date de publication:
Mar 2023
Historique:
revised: 02 12 2022
received: 19 07 2022
accepted: 09 12 2022
pubmed: 22 12 2022
medline: 15 3 2023
entrez: 21 12 2022
Statut: ppublish

Résumé

The administration of intermittent parathyroid hormone (iPTH) is anabolic to the skeleton. Recent studies with cultured osteoblasts have revealed that the expression of PHOSPHO1, a bone-specific phosphatase essential for the initiation of mineralisation, is regulated by PTH. Therefore, this study sought to determine whether the bone anabolic response to iPTH involves modulation of expression of Phospho1 and of other enzymes critical for bone matrix mineralisation. To mimic iPTH treatment, primary murine osteoblasts were challenged with 50 nM PTH for 6 h in every 48 h period for 8 days (4 cycles), 14 days (7 cycles) and 20 days (10 cycles) in total. The expression of both Phospho1 and Smpd3 was almost completely inhibited after 4 cycles, whereas 10 cycles were required to stimulate a similar response in Alpl expression. To explore the in vivo role of PHOSPHO1 in PTH-mediated osteogenesis, the effects of 14- and 28-day iPTH (80 µg/kg/day) administration was assessed in male wild-type (WT) and Phospho1

Identifiants

pubmed: 36540015
doi: 10.1002/cbf.3772
doi:

Substances chimiques

Parathyroid Hormone 0
Alkaline Phosphatase EC 3.1.3.1
Smpd3 protein, mouse EC 3.1.4.12
Sphingomyelin Phosphodiesterase EC 3.1.4.12
PHOSPHO1 protein, mouse EC 3.1.3.-
Phosphoric Monoester Hydrolases EC 3.1.3.2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

189-201

Subventions

Organisme : BB/J004316/1
Organisme : BB/J01446X/1
Organisme : Biotechnology and Biological Sciences Research Council
Pays : United Kingdom

Informations de copyright

© 2022 The Authors. Cell Biochemistry and Function published by John Wiley & Sons Ltd.

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Auteurs

Dean A Houston (DA)

Functional Genetics Division, The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Midlothian, UK.

Louise A Stephen (LA)

Functional Genetics Division, The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Midlothian, UK.

Soher N Jayash (SN)

Functional Genetics Division, The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Midlothian, UK.

Katherine Myers (K)

Functional Genetics Division, The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Midlothian, UK.

Kirsty Little (K)

Functional Genetics Division, The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Midlothian, UK.

Mark Hopkinson (M)

Comparative Biomedical Sciences, The Royal Veterinary College, London, UK.

Andrew A Pitsillides (AA)

Comparative Biomedical Sciences, The Royal Veterinary College, London, UK.

Vicky E MacRae (VE)

Functional Genetics Division, The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Midlothian, UK.

Jose Luis Millan (JL)

Human Genetics Program, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, California, USA.

Katherine A Staines (KA)

School of Applied Sciences, Centre for Stress and Age-Related Disease, University of Brighton, Brighton, UK.

Colin Farquharson (C)

Functional Genetics Division, The Roslin Institute and Royal (Dick) School of Veterinary Studies, University of Edinburgh, Midlothian, UK.

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Classifications MeSH