Cells Derived from Human Long Bone Appear More Differentiated and More Actively Stimulate Osteoclastogenesis Compared to Alveolar Bone-Derived Cells

• Published in: International journal of molecular sciences Vol. 21; no. 14; p. 5072
• Main Authors: Kelder, Cindy, Kleverlaan, Cornelis J, Gilijamse, Marjolijn, Bakker, Astrid D, de Vries, Teun J
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 17.07.2020; MDPI
• Subjects: Actin; Alveolar bone; Alveolar Process - cytology; Biomedical materials; Bisphosphonates; Bone growth; Bone remodeling; Bones; calcitriol; Cell culture; Cell Differentiation; Cell Proliferation; Cells, Cultured; Communication; Cytoskeleton; DC-STAMP protein; Dendritic cells; Deoxyribonucleic acid; DNA; Gene expression; Humans; jaw bone; Leukocytes (mononuclear); Long bone; Osteoblasts; Osteoblasts - cytology; Osteoclastogenesis; Osteoclasts; Osteoclasts - cytology; Osteogenesis; Osteopontin; Periodontitis; Peripheral blood mononuclear cells; Phenotypes; Phosphates; Proteins; Regeneration; Stem cells; Tibia - cytology; Tissue engineering; TRANCE protein; Tumor necrosis factor-α; Vitamin D3; cell differentiation; osteoblasts; calcitriol; jaw bone; osteoclasts; vitamin D3
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms21145072

Osteoblasts derived from mouse skulls have increased osteoclastogenic potential compared to long bone osteoblasts when stimulated with 1,25(OH) vitamin D (vitD ). This indicates that bone cells from specific sites can react differently to biochemical signals, e.g., during inflammation or as emitted by bioactive bone tissue-engineering constructs. Given the high turn-over of alveolar bone, we hypothesized that alveolar bone-derived osteoblasts have an increased osteogenic and osteoclastogenic potential compared to the osteoblasts derived from long bone. The osteogenic and osteoclastogenic capacity of alveolar bone cells and long bone cells were assessed in the presence and absence of osteotropic agent vitD . Both cell types were studied in osteogenesis experiments, using an osteogenic medium, and in osteoclastogenesis experiments by co-culturing osteoblasts with peripheral blood mononuclear cells (PBMCs). Both osteogenic and osteoclastic markers were measured. At day 0, long bones seem to have a more late-osteoblastic/preosteocyte-like phenotype compared to the alveolar bone cells as shown by slower proliferation, the higher expression of the matrix molecule ( and the osteocyte-enriched cytoskeletal component ( . This phenotype was maintained during the osteogenesis assays, where long bone-derived cells still expressed more and . Under co-culture conditions with PBMCs, long bone cells also had a higher ( ) expression and induced the formation of osteoclasts more than alveolar bone cells. Correspondingly, the expression of osteoclast genes ( ) and was higher in long bone co-cultures. Together, our results indicate that long bone-derived osteoblasts are more active in bone-remodeling processes, especially in osteoclastogenesis, than alveolar bone-derived cells. This indicates that tissue-engineering solutions need to be specifically designed for the site of application, such as defects in long bones vs. the regeneration of alveolar bone after severe periodontitis.