eCM (Eur Cell Mater / e Cells & Materials) Not-for-profit Open Access
Created by Scientists, for Scientists
 ISSN:1473-2262         NLM:100973416 (link)         DOI:10.22203/eCM

2011   Volume No 21 – pages 80-93

Title: Development of an osteoblast/osteoclast co-culture derived by human bone marrow stromal cells and human monocytes for biomaterials testing

Author: C Heinemann, S Heinemann, H Worch, T Hanke

Address: Max Bergmann Center of Biomaterials and Institute of Materials Science, Dresden University of Technology, D-01069 Dresden, Germany

E-mail: christiane.heinemann at tu-dresden.de

Key Words: human bone marrow stromal cells, osteoblasts, human monocytes, osteoclasts, osteoclastogenesis, co-cultivation, biocompatibility, bone remodelling, cross talk, biomaterial, xerogel.

Publication date: January 25th 2011

Abstract: The communication of bone-forming osteoblasts and bone-resorbing osteoclasts is a fundamental requirement for balanced bone remodelling. For biomaterial research, development of in vitro models is necessary to investigate this communication. In the present study human bone marrow stromal cells and human monocytes were cultivated in order to differentiate into osteoblasts and osteoclasts, respectively. Finally, a cultivation regime was identified which firstly induces the differentiation of the human bone marrow stromal cells followed by the induction of osteoclastogenesis through the osteoblasts formed – without the external addition of the factors RANKL and M-CSF. As a feedback on osteoblasts enhanced gene expression of BSP II was detected for modifications which facilitated the formation of large multinuclear osteoclasts. Phenotype characterization was performed by biochemical methods (DNA, LDH, ALP, TRAP 5b), gene expression analysis (ALP, BSP II, RANKL, IL-6, VTNR, CTSK, TRAP, OSCAR, CALCR) as well as light microscopy, confocal laser scanning microscopy, and scanning electron microscopy. After establishing this model on polystyrene, similar positive results were obtained for cultivation on a relevant bone substitution material – a composite xerogel of silica, collagen, and calcium phosphate.

Article download: Pages 80-93 (PDF file)
DOI: 10.22203/eCM.v021a07