Effects of culture conditions on osteogenic differentiation in human mesenchymal stem cells

Authors
Song, Su JinJeon, OjuYang, Hee SeokHan, Dong KeunKim, Byung-Soo
Issue Date
2007-07
Publisher
KOREAN SOC MICROBIOLOGY & BIOTECHNOLOGY
Citation
JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY, v.17, no.7, pp.1113 - 1119
Abstract
Human bone marrow-derived mesenchymal stern cells (hBMMSCs) must differentiate into osteogenic cells to allow for successful bone regeneration. In this study, we investigated the effects of different combinations of three soluble osteogenic differentiation-inducing factors [L-ascorbic acid (AC), beta-glycerophosphate (PG), and bone morphogenic protein-2 (BMP-2)] and the presence of a hydroxyapatite (HA) substrate on hBMMSC osteogenic differentiation in vitro. hBMMSCs were cultured in medium containing various combinations of the soluble factors on culture plates with or without HA coating. After 7 days of culture, alkaline phosphatase (ALP) activity, calcium deposition, and osteoprotegerin (OPG) and osteopontin (OPN) expression were measured. The effects of individual and combined factors were evaluated using a factorial analysis method. BMP-2 predominantly affected expression of early markers of osteogenic differentiation (ALP and OPG). HA had the highest positive effect on OPN expression and calcium deposition. The interaction between AC, beta G and HA had the second highest positive effect on ALP activity.
Keywords
MARROW STROMAL CELLS; SIGNAL-REGULATED KINASE; BONE-MARROW; IN-VITRO; ALKALINE-PHOSPHATASE; COMPOSITE SCAFFOLDS; OSTEOBLAST PHENOTYPE; PROLIFERATION; PLASMA; GROWTH; MARROW STROMAL CELLS; SIGNAL-REGULATED KINASE; BONE-MARROW; IN-VITRO; ALKALINE-PHOSPHATASE; COMPOSITE SCAFFOLDS; OSTEOBLAST PHENOTYPE; PROLIFERATION; PLASMA; GROWTH; bone; differentiation; mesenchymal stem cell
ISSN
1017-7825
URI
https://pubs.kist.re.kr/handle/201004/134292
Appears in Collections:
KIST Article > 2007
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