The Role of Calcium and Nicotinic Acid Adenine Dinucleotide Phosphate (NAADP) in Human Osteoclast Formation and Resorption

Verfasser / Beitragende:
[X. Cheng, E. Hookway, T. Kashima, U. Oppermann, A. Galione, N. Athanasou]
Ort, Verlag, Jahr:
2015
Enthalten in:
Calcified Tissue International, 96/1(2015-01-01), 73-79
Format:
Artikel (online)
ID: 605521077
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024 7 0 |a 10.1007/s00223-014-9939-3  |2 doi 
035 |a (NATIONALLICENCE)springer-10.1007/s00223-014-9939-3 
245 0 4 |a The Role of Calcium and Nicotinic Acid Adenine Dinucleotide Phosphate (NAADP) in Human Osteoclast Formation and Resorption  |h [Elektronische Daten]  |c [X. Cheng, E. Hookway, T. Kashima, U. Oppermann, A. Galione, N. Athanasou] 
520 3 |a Osteoclasts are specialised bone resorbing cells which form by fusion of circulating mononuclear phagocyte precursors. Bone resorption results in the release of large amounts of calcium into the extracellular fluid (ECF), but it is not certain whether changes in extracellular calcium concentration [Ca2+]e influence osteoclast formation and resorption. In this study, we sought to determine the effect of [Ca2+]e and NAADP, a potent calcium mobilising messenger that induces calcium uptake, on human osteoclast formation and resorption. CD14+ human monocytes were cultured with M-CSF and RANKL in the presence of different concentrations of calcium and NAADP and the effect on osteoclast formation and resorption evaluated. We found that the number of TRAP+ multinucleated cells and the extent of lacunar resorption were reduced when there was an increase in extracellular calcium and NAADP. This was associated with a decrease in RANK mRNA expression by CD14+ cells. At high concentrations (20mM) of [Ca2+]e mature osteoclast resorption activity remained unaltered relative to control cultures. Our findings indicate that osteoclast formation is inhibited by a rise in [Ca2+]e and that RANK expression by mononuclear phagocyte osteoclast precursors is also [Ca2+]e dependent. Changes in NAADP also influence osteoclast formation, suggesting a role for this molecule in calcium handling. Osteoclasts remained capable of lacunar resorption, even at high ECF [Ca2+]e, in keeping with their role in physiological and pathological bone resorption. 
540 |a Springer Science+Business Media New York, 2014 
690 7 |a Calcium  |2 nationallicence 
690 7 |a Osteoclast  |2 nationallicence 
690 7 |a NAADP  |2 nationallicence 
690 7 |a RANK  |2 nationallicence 
700 1 |a Cheng  |D X.  |u Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Nuffield Orthopaedic Centre, University of Oxford, OX3 7LD, Oxford, UK  |4 aut 
700 1 |a Hookway  |D E.  |u Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Nuffield Orthopaedic Centre, University of Oxford, OX3 7LD, Oxford, UK  |4 aut 
700 1 |a Kashima  |D T.  |u Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Nuffield Orthopaedic Centre, University of Oxford, OX3 7LD, Oxford, UK  |4 aut 
700 1 |a Oppermann  |D U.  |u Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Nuffield Orthopaedic Centre, University of Oxford, OX3 7LD, Oxford, UK  |4 aut 
700 1 |a Galione  |D A.  |u Department of Pharmacology, University of Oxford, OX1 3QT, Oxford, UK  |4 aut 
700 1 |a Athanasou  |D N.  |u Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Nuffield Orthopaedic Centre, University of Oxford, OX3 7LD, Oxford, UK  |4 aut 
773 0 |t Calcified Tissue International  |d Springer US; http://www.springer-ny.com  |g 96/1(2015-01-01), 73-79  |x 0171-967X  |q 96:1<73  |1 2015  |2 96  |o 223 
856 4 0 |u https://doi.org/10.1007/s00223-014-9939-3  |q text/html  |z Onlinezugriff via DOI 
898 |a BK010053  |b XK010053  |c XK010000 
900 7 |a Metadata rights reserved  |b Springer special CC-BY-NC licence  |2 nationallicence 
908 |D 1  |a research-article  |2 jats 
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950 |B NATIONALLICENCE  |P 700  |E 1-  |a Cheng  |D X.  |u Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Nuffield Orthopaedic Centre, University of Oxford, OX3 7LD, Oxford, UK  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Hookway  |D E.  |u Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Nuffield Orthopaedic Centre, University of Oxford, OX3 7LD, Oxford, UK  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Kashima  |D T.  |u Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Nuffield Orthopaedic Centre, University of Oxford, OX3 7LD, Oxford, UK  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Oppermann  |D U.  |u Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Nuffield Orthopaedic Centre, University of Oxford, OX3 7LD, Oxford, UK  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Galione  |D A.  |u Department of Pharmacology, University of Oxford, OX1 3QT, Oxford, UK  |4 aut 
950 |B NATIONALLICENCE  |P 700  |E 1-  |a Athanasou  |D N.  |u Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Nuffield Orthopaedic Centre, University of Oxford, OX3 7LD, Oxford, UK  |4 aut 
950 |B NATIONALLICENCE  |P 773  |E 0-  |t Calcified Tissue International  |d Springer US; http://www.springer-ny.com  |g 96/1(2015-01-01), 73-79  |x 0171-967X  |q 96:1<73  |1 2015  |2 96  |o 223