Jci_page_head_homepage_01 Jci_page_head_homepage_02
Naoshi Ogata, Daichi Chikazu, Naoto Kubota, Yasuo Terauchi, Kazuyuki Tobe, Yoshiaki Azuma, Tomohiro Ohta, Takashi Kadowaki, Kozo Nakamura, Hiroshi Kawaguchi
Published in Volume 105, Issue 7
J Clin Invest. 2000; 105(7):935–943 doi:10.1172/JCI9017
Abstract | Full text | PDF
Options: View larger image (or click on image)
Medium
Figure 4

Cultures of osteoblasts from WT and IRS-1–/– mice. (a) Cell proliferation of cultured osteoblasts. Osteoblasts from neonatal calvariae of WT and IRS-1–/– littermates were cultured with or without IGF-I (10 nM), insulin (100 nM), or FGF-2 (1 nM) for 24 hours, and the cell proliferation was determined by [3H]-TdR incorporation into DNA. (b) ALP activity of osteoblasts from WT or IRS-1–/– neonatal calvariae cultured with or without IGF-I (10 nM), insulin (100 nM), or BMP-2 (30 ng/mL) at 14 days of culture. Data are expressed as mean (bars) ± SEM (error bars) for 8 wells/group. Significantly different from WT cultures, AP < 0.05, BP < 0.01.