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Aldemar Montero, Yosuke Okada, Masato Tomita, Masako Ito, Hiroshi Tsurukami, Toshitaka Nakamura, Thomas Doetschman, J. Douglas Coffin, Marja M. Hurley
Published in Volume 105, Issue 8
J Clin Invest. 2000; 105(8):1085–1093 doi:10.1172/JCI8641
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Figure 2

Comparison of thymidine incorporation into DNA in calvarial osteoblasts from 8-week-old Fgf2+/+ and Fgf2–/– mice. Osteoblastic cells were prepared from calvariae of 8-week-old Fgf2+/+ and Fgf2–/– mice and plated in 100-mm dishes in DMEM with 10% heat inactivated FCS for 12 days. Cells were harvested and replated at a density of 5,000 cells/cm2 for 7 days. Media were changed every 3 days. Cultures were treated with fresh media in the absence or presence of FGF-2 (10 nM) for the last 24 hours of the culture period. For labeling studies, [3H]thymidine (10 μCi/well) was added for the last 4 hours of the culture to measure thymidine incorporation into DNA. Values are the mean ± SEM for 6 determinations per group. ASignificantly different from control cultures; P < 0.05. BSignificantly different from Fgf2+/+; P < 0.05.