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The role of apoptosis in mineralizing murine versus avian micromass culture systems. | LitMetric

The role of apoptosis in mineralizing murine versus avian micromass culture systems.

J Cell Biochem

Hospital for Special Surgery, 535 E 70th Street, Caspary Research, New York, New York 10021, USA.

Published: October 2010

AI Article Synopsis

Article Abstract

Chondrocyte apoptosis is thought to be an important step in the calcification of cartilage in vivo; however, there are conflicting reports as to whether or not this apoptosis is a necessary precursor to mineralization. The goal of this study was to determine whether or not apoptosis is necessary for mineralization in an in vitro murine micromass model of endochondral ossification. C3H10T1/2 murine mesenchymal stem cells were plated in micromass culture in the presence of 4 mM inorganic phosphate with the addition of the apoptogens, camptothecin, or staurosporine, to induce apoptosis. The rate and total accumulation of mineralization was measured with (45)Ca uptake. In these studies, both apoptogens increased the rate of mineralization, with staurosporine increasing (45)Ca accumulation by about 2.5 times that of controls and camptothecin increasing total amounts of mineralization about 1.5 times that of controls. Inhibiting cell apoptosis with the caspase inhibitor, ZVAD-fmk, to prevent apoptosis, caused slower rates of (45)Ca uptake; however, total amounts of (45)Ca accumulation reached the same values by day 30 of culture. FTIR data showed mineralization in all samples treated with 4 mM inorganic phosphate, with the highest mineral to matrix ratios in the camptothecin treated samples.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2946502PMC
http://dx.doi.org/10.1002/jcb.22748DOI Listing

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