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Published 1 October 2001. doi:10.1083/jcb1551iti6
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© The Rockefeller University Press, 0021-9525/2001/10/10-b $5.00
The Journal of Cell Biology, Volume 155, Number 1, October 1, 2001 10-b-10


In This Issue

Bone breakage


More marrow and weaker bones in mice with excess Cbfa1 (right).

Many growth factors that promote the formation of bone-forming cells called osteoblasts are thought to act through a transcription factor called core binding factor {alpha}1 (Cbfa1). Mice lacking Cbfa1 fail to form any mature osteoblasts or bones, and experiments with a dominant negative form of Cbfa1 have suggested that the protein is important in regulating osteoblast functions such as matrix formation and mineralization.

Now, Liu et al. (page 157) find that mice overexpressing Cbfa1 in their osteoblasts have weak bones and multiple fractures within a few weeks after birth. Immature osteoblasts accumulate, suggesting that the excess Cbfa1 inhibits a late stage of osteoblast maturation. Thus, Cbfa1 is essential early in maturation but must then be downregulated to allow final maturation. {blacksquare}



William A. Wells

wellsw{at}rockefeller.edu


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Related Article

Overexpression of Cbfa1 in osteoblasts inhibits osteoblast maturation and causes osteopenia with multiple fractures
Wenguang Liu, Satoru Toyosawa, Tatsuya Furuichi, Naoko Kanatani, Carolina Yoshida, Yang Liu, Miki Himeno, Satoru Narai, Akira Yamaguchi, and Toshihisa Komori
J. Cell Biol. 2001 155: 157-166. [Abstract] [Full Text] [PDF]




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