TY - JOUR
T1 - Comparison of fetal and adult marrow stromal cells in osteogenesis with and without glucocorticoids
AU - Chang, Pi Ling
AU - Blair, Harry C.
AU - Zhao, Xiaochu
AU - Chien, Yi Wen
AU - Chen, Dung Tsa
AU - Tilden, Arabella B.
AU - Chang, Zhijie
AU - Cao, Xu
AU - Faye-Petersen, Ona Marie
AU - Hicks, Patricia
N1 - Funding Information:
Research Center of Oral Biology, University of Alabama at Birmingham, contract grant sponsor: National Institute of Health; contract grant number: CA69688, CA90920, AG12951, and AR47700, and the Department of Veterans affairs. There is no conflict of interest that would prejudice its impartiality.
PY - 2006/3
Y1 - 2006/3
N2 - To better understand the potential use of fetal marrow stromal cells (MSCs) in bone tissue engineering, we compared the ability of these cells with those of adult MSCs with respect to osteoblasts differentiation in the presence or absence of glucocorticoids. Cells were grown for 3 - 4 weeks in basal medium or supplemented with 100 nM dexamethasone (DEX, a synthetic glucocorticoid analog) or with 50 μM L-ascorbate and 10 mM glycerol-2-phosphate (AS+GP) or with AS+GP+DEX. At various time points in culture, the following parameters were compared between fetal and adult MSCs: cell morphology, cell proliferation, alkaline phosphatase activity, calcium (45Ca) uptake, von Kossa staining, and glucocorticoids receptor expression were analyzed. Compared with adult MSCs, fetal cells showed a less dramatic change to cuboidal morphology in DEX-containing media. Fetal MSCs in all media conditions showed higher proliferation rates and lower alkaline phosphatase activities (p < 0.001) than adult cells. Both fetal and adult MSCs responded similarly in DEX-containing media with respect to suppressing cell proliferation, stimulating alkaline phosphatase activity, and consistently accumulating calcium (usually higher in fetal cells) with subsequent formation of mineralized matrix when compared with cells cultured in AS+GP. Our findings further implicate the requirement of glucocorticoids in osteogenesis. In conclusion, compared with adult MSCs, fetal cells showed greater ability in sustaining cell proliferation and calcium uptake suggesting that they may be useful for bone tissue repair.
AB - To better understand the potential use of fetal marrow stromal cells (MSCs) in bone tissue engineering, we compared the ability of these cells with those of adult MSCs with respect to osteoblasts differentiation in the presence or absence of glucocorticoids. Cells were grown for 3 - 4 weeks in basal medium or supplemented with 100 nM dexamethasone (DEX, a synthetic glucocorticoid analog) or with 50 μM L-ascorbate and 10 mM glycerol-2-phosphate (AS+GP) or with AS+GP+DEX. At various time points in culture, the following parameters were compared between fetal and adult MSCs: cell morphology, cell proliferation, alkaline phosphatase activity, calcium (45Ca) uptake, von Kossa staining, and glucocorticoids receptor expression were analyzed. Compared with adult MSCs, fetal cells showed a less dramatic change to cuboidal morphology in DEX-containing media. Fetal MSCs in all media conditions showed higher proliferation rates and lower alkaline phosphatase activities (p < 0.001) than adult cells. Both fetal and adult MSCs responded similarly in DEX-containing media with respect to suppressing cell proliferation, stimulating alkaline phosphatase activity, and consistently accumulating calcium (usually higher in fetal cells) with subsequent formation of mineralized matrix when compared with cells cultured in AS+GP. Our findings further implicate the requirement of glucocorticoids in osteogenesis. In conclusion, compared with adult MSCs, fetal cells showed greater ability in sustaining cell proliferation and calcium uptake suggesting that they may be useful for bone tissue repair.
KW - Alkaline phosphatase
KW - Calcium uptake
KW - Dexamethasone
KW - Fetal and adult marrow stromal cells
KW - Glucocorticoid receptor mRNA
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U2 - 10.1080/03008200600584074
DO - 10.1080/03008200600584074
M3 - Article
C2 - 16754512
AN - SCOPUS:33744921100
SN - 0300-8207
VL - 47
SP - 67
EP - 76
JO - Connective tissue research
JF - Connective tissue research
IS - 2
ER -