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  4. Osteoidosis leads to altered differentiation and function of osteoclasts
 
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Osteoidosis leads to altered differentiation and function of osteoclasts

Citation Link: https://doi.org/10.15480/882.3050
Publikationstyp
Journal Article
Date Issued
2020-04-13
Sprache
English
Author(s)
Grünherz, Lisanne  
Prein, Carina  
Winkler, Thomas  
Kirsch, Manuela  
Hopfner, Ursula  
Streichert, Thomas  
Clausen-Schaumann, Hauke  
Zustin, Jozef  
Kirchhof, Kristin  
Morlock, Michael M.  
Machens, Hans-Günther  
Schilling, Arndt Friedrich  
Institut
Biomechanik M-3  
TORE-DOI
10.15480/882.3050
TORE-URI
http://hdl.handle.net/11420/7767
Journal
Journal of cellular and molecular medicine  
Volume
24
Issue
10
Start Page
5665
End Page
5674
Citation
Journal of Cellular and Molecular Medicine 10 (24): 5665-5674 (2020)
Publisher DOI
10.1111/jcmm.15227
Scopus ID
2-s2.0-85083310361
PubMed ID
32283567
Publisher
Wiley-Blackwell
In patients with osteomalacia, a defect in bone mineralization leads to changed characteristics of the bone surface. Considering that the properties of the surrounding matrix influence function and differentiation of cells, we aimed to investigate the effect of osteoidosis on differentiation and function of osteoclasts. Based on osteomalacic bone biopsies, a model for osteoidosis in vitro (OIV) was established. Peripheral blood mononuclear cells were differentiated to osteoclasts on mineralized surfaces (MS) as internal control and on OIV. We observed a significantly reduced number of osteoclasts and surface resorption on OIV. Atomic force microscopy revealed a significant effect of the altered degree of mineralization on surface mechanics and an unmasking of collagen fibres on the surface. Indeed, coating of MS with RGD peptides mimicked the resorption phenotype observed in OIV, suggesting that the altered differentiation of osteoclasts on OIV might be associated with an interaction of the cells with amino acid sequences of unmasked extracellular matrix proteins containing RGD sequences. Transcriptome analysis uncovered a strong significant up-regulation of transmembrane glycoprotein TROP2 in osteoclastic cultures on OIV. TROP2 expression on OIV was also confirmed on the protein level and found on the bone surface of patients with osteomalacia. Taken together, our results show a direct influence of the mineralization state of the extracellular matrix surface on differentiation and function of osteoclasts on this surface which may be important for the pathophysiology of osteomalacia and other bone disorders with changed ratio of osteoid to bone.
Subjects
mechanotransduction
osteoclast
osteomalacia
RGD peptide
vitamin D
DDC Class
570: Biowissenschaften, Biologie
Publication version
submittedVersion
Lizenz
https://creativecommons.org/licenses/by/4.0/
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