Details zur Publikation

Referenztyp Zeitschriften
DOI / URL Link
Titel (primär) The effect of the degree of sulfation of glycosaminoglycans on osteoclast function and signaling pathways
Autor Salbach, J.; Kliemt, S.; Rauner, M.; Rachner, T.D.; Goettsch, C.; Kalkhof, S.; von Bergen, M.; Möller, S.; Schnabelrauch, M.; Hintze, V.; Scharnweber, D.; Hofbauer, L.C.;
Journal / Serie Biomaterials
Erscheinungsjahr 2012
Department PROTEOM;
Band/Volume 33
Heft 33
Sprache englisch;
Keywords Extracellular matrix (ECM); Chondroitin sulfate; Hyaluronan; Osteoclast; Sulfated glycosaminoglycans; Quantitative proteomics
Abstract To meet the growing need for bone replacement of our aging population, development of new adaptive biomaterials is essential. Collagen and glycosaminoglycans (GAGs) such as hyaluronan (HA) and chondroitin sulfate (CS) are major components of the extracellular matrix (ECM) in bone. We manufactured native and sulfate-modified GAG matrices, evaluated how these components modulate different functions of osteoclasts, the cells that resorb bone, and analyzed the underlying mechanisms. GAGs were tested for their effects on osteoclast adhesion, viability, differentiation, morphology, and resorption as well as proteome alterations using murine RAW264.7 cells and primary human osteoclasts. Native and sulfated GAGs were stable and largely non-cytotoxic. Sulfation of GAGs led to a significant inhibition of osteoclast differentiation and resorption, which was largely dependent on the degree of sulfation of GAGs rather than the monosaccharide composition. Sulfation significantly reduced resorptive function by 14% (CS) and 43% (HA). Highly sulfated GAGs dose-dependently suppressed osteoclast differentiation, osteoclast-specific expression of TRAP, cathepsin K, SWAP-70, and OSCAR by 63–95%, and inhibited proteins involved in cytoskeletal rearrangement. In conclusion, highly sulfated GAGs significantly inhibit various functions of bone-resorbing osteoclasts. Whether these properties locally contribute to improved fracture or bone defect healing needs to be validated in vivo.

ID 12923
dauerhafte UFZ-Verlinkung https://www.ufz.de/index.php?en=20939&ufzPublicationIdentifier=12923
Salbach, J., Kliemt, S., Rauner, M., Rachner, T.D., Goettsch, C., Kalkhof, S., von Bergen, M., Möller, S., Schnabelrauch, M., Hintze, V., Scharnweber, D., Hofbauer, L.C. (2012):
The effect of the degree of sulfation of glycosaminoglycans on osteoclast function and signaling pathways
Biomaterials 33 (33), 8418 - 8429