In vitro dexamethasone pretreatment enhances bone formation of human mesenchymal stem cells in vivo

Bone grafting is the current standard of care for treatment of fracture nonunions, while alternative strategies such as bone marrow‐derived mesenchymal stem cells are also used. MSCs can be induced towards the osteogenic lineage by in vitro treatment with dexamethasone (dex). This study aimed to det...

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Veröffentlicht in:Journal of orthopaedic research 2009-07, Vol.27 (7), p.916-921
Hauptverfasser: Song, In-Hwan, Caplan, Arnold I., Dennis, James E.
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container_title Journal of orthopaedic research
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creator Song, In-Hwan
Caplan, Arnold I.
Dennis, James E.
description Bone grafting is the current standard of care for treatment of fracture nonunions, while alternative strategies such as bone marrow‐derived mesenchymal stem cells are also used. MSCs can be induced towards the osteogenic lineage by in vitro treatment with dexamethasone (dex). This study aimed to determine the optimal duration of dex treatment for osteogenic differentiation of MSCs in vitro and evaluate the effect of this dex pretreatment on bone formation in vivo. To determine the optimal dex treatment, MSCs were cultivated in osteogenic medium for 5 weeks with a varying dex withdrawal schedule, such that MSCs were exposed to dex for either 0, 1, 2, 3, 4, or 5 weeks. During this period, alkaline phosphatase, calcium, and DNA assays, as well as von Kossa staining and morphological observations were performed. One and 2 week dex‐treated groups returned to control levels rapidly, whereas 3 and 4 week groups retained higher levels of differentiation markers, with the 4 week group being the highest. Based on these in vitro results, MSCs (with and without dex) and control fibroblasts were seeded into ceramic cubes, cultured for 4 weeks, and implanted into SCID mice, and harvested 6 weeks postimplantation for histologic evaluation. There was no bone formation in fibroblast‐seeded controls, little bone formation in control (CS 1), and extensive bone formation (CS 3–4) in dex‐treated MSCs. These results indicate that pretreatment of MSCs with dex results in greater bone formation than in untreated controls. © 2009 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 27: 916–921, 2009
doi_str_mv 10.1002/jor.20838
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MSCs can be induced towards the osteogenic lineage by in vitro treatment with dexamethasone (dex). This study aimed to determine the optimal duration of dex treatment for osteogenic differentiation of MSCs in vitro and evaluate the effect of this dex pretreatment on bone formation in vivo. To determine the optimal dex treatment, MSCs were cultivated in osteogenic medium for 5 weeks with a varying dex withdrawal schedule, such that MSCs were exposed to dex for either 0, 1, 2, 3, 4, or 5 weeks. During this period, alkaline phosphatase, calcium, and DNA assays, as well as von Kossa staining and morphological observations were performed. One and 2 week dex‐treated groups returned to control levels rapidly, whereas 3 and 4 week groups retained higher levels of differentiation markers, with the 4 week group being the highest. Based on these in vitro results, MSCs (with and without dex) and control fibroblasts were seeded into ceramic cubes, cultured for 4 weeks, and implanted into SCID mice, and harvested 6 weeks postimplantation for histologic evaluation. There was no bone formation in fibroblast‐seeded controls, little bone formation in control (CS 1), and extensive bone formation (CS 3–4) in dex‐treated MSCs. These results indicate that pretreatment of MSCs with dex results in greater bone formation than in untreated controls. © 2009 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. 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Orthop. Res</addtitle><description>Bone grafting is the current standard of care for treatment of fracture nonunions, while alternative strategies such as bone marrow‐derived mesenchymal stem cells are also used. MSCs can be induced towards the osteogenic lineage by in vitro treatment with dexamethasone (dex). This study aimed to determine the optimal duration of dex treatment for osteogenic differentiation of MSCs in vitro and evaluate the effect of this dex pretreatment on bone formation in vivo. To determine the optimal dex treatment, MSCs were cultivated in osteogenic medium for 5 weeks with a varying dex withdrawal schedule, such that MSCs were exposed to dex for either 0, 1, 2, 3, 4, or 5 weeks. During this period, alkaline phosphatase, calcium, and DNA assays, as well as von Kossa staining and morphological observations were performed. 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source Wiley Online Library - AutoHoldings Journals; MEDLINE; Wiley Online Library Free Content
subjects Adolescent
Adult
Animals
bone formation
Cell Differentiation - drug effects
Cell Lineage - drug effects
Cells, Cultured
Ceramics
dexamethasone
Dexamethasone - pharmacology
Diffusion Chambers, Culture
Glucocorticoids - pharmacology
Humans
Ilium - cytology
In Vitro Techniques
Mesenchymal Stem Cell Transplantation - methods
mesenchymal stem cells
Mesenchymal Stromal Cells - cytology
Mesenchymal Stromal Cells - drug effects
Mice
Mice, SCID
Middle Aged
Osteocytes - cytology
Osteogenesis - drug effects
Young Adult
title In vitro dexamethasone pretreatment enhances bone formation of human mesenchymal stem cells in vivo
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