Selection of malonate-resistant stromal cell-derived osteoprogenitor cells in vitro

✍ Scribed by Benjamin Y. Klein; Irena Gal; David Segal

• Publisher: John Wiley and Sons
• Year: 1993
• Tongue: English
• Weight: 742 KB
• Volume: 51
• Category: Article
• ISSN: 0730-2312
• DOI: 10.1002/jcb.240510211

✦ Synopsis

Bone marrow stromal cells give rise to osteoprogenitor cell (OPC) colonies, with characteristic mineralized bone nodules in vitro. During differentiation, OPCs in the culture are surrounded by heterogeneous populations of various cell lineages and by different OPC differentiation stages In the present study, attempts were made to increase the homogeneity of OPCs in culture The reliance on energy metabolism restricted to glycolysis, which is specific to the premineralizing skeletal cells, was tested as a selectable marker for cells in this stage Day 12 alkaline phosphatase (ALP) and day 20-21 calcium precipitates were used as early and late OPC differentiation markers Malonate, a competitive inhibitor of succinate dehydrogenase, was added to the OPC stimulation medium, to interfere with the Krebs cycle-dependent energy metabolism operating in most of the stromal cells OPCs that entered the stage of energy metabolism restricted to glycolysis were expected to become malonate resistant Malonate showed dose and time dependence, 10 m M malonate added on day 3, decreased day 12 ALP activity/well to the lowest level Variations in time and length of exposure to malonate used during the first 12 days of differentiation showed an inverse correlation between specific ALP activity and cell yield. Malonate-treated variations of specific ALP and of cell yield indices were up to 30-to 40-fold larger than variations within day 21 calcium precipitates. Thus, calcifying cells were almost unchanged relatively to noncalcifying cells. These results indicate that malonate-resistant cells are mostly selected, rather than induced, to differentiate by malonate. The results also show that stromal derived OPCs undergo a similar biochemical stage as in chondrocytes T 1993 WiIey-Liss, Inc