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Published as doi: 10.1096/fj.06-7571com.
(The FASEB Journal. 2007;21:1777-1787.)
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Identification of a potent combination of osteogenic genes for bone regeneration using embryonic stem (ES) cell-based sensor

Shinsuke Ohba*,{dagger},{ddagger}, Toshiyuki Ikeda{dagger}, Fumitaka Kugimiya{dagger},{ddagger}, Fumiko Yano{dagger},{ddagger}, Alexander C. Lichtler§, Kozo Nakamura{dagger}, Tsuyoshi Takato{dagger}, Hiroshi Kawaguchi{dagger} and Ung-il Chung{ddagger},1

* Japan Society for the Promotion of Science (JSPS), Chiyoda-ku, Tokyo, Japan;

{dagger} Division of Sensory and Motor System Medicine and

{ddagger} Center for Disease Biology and Integrative Medicine, Faculty of Medicine, the University of Tokyo, Hongo, Bunkyo-ku, Tokyo, Japan; and

§ Department of Genetics and Developmental Biology, University of Connecticut Health Center, Farmington, Connecticut, USA

1Correspondence: Center for Disease Biology and Integrative Medicine, Faculty of Medicine, the University of Tokyo, 7–3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan. E-mail: uichung-tky{at}umin.ac.jp

To identify potent bioactive factors for in vivo tissue regeneration by comprehensive screening remains a challenge for regenerative medicine. Here we report the development of an ES cell-based monitoring system for osteogenic differentiation, the identification of a potent combination of osteogenic genes using such a system, and an evaluation of its therapeutic potentials. ES cells were isolated from mice carrying a transgene expressing GFP driven by the 2.3 kb fragment of rat type I collagen {alpha}(1) promoter. Using these cells engineered to fluoresce on osteogenic differentiation, we screened cDNA libraries and combinations of major osteogenesis-related genes. Among them, the combination of constitutively active activin receptor-like kinase 6 (caALK6) and runt-related transcription factor 2 (Runx2) was the minimal unit that induced fluorescence. The combination efficiently induced osteogenic differentiation in various cell types, including terminally differentiated nonosteogenic cells. The cooperative action of the combination occurred through protein stabilization of core binding factor beta (Cbfb), induction of Runx2-Cbfb complex formation, and its DNA binding. Furthermore, transplantation of a monolayer sheet of fibroblasts transduced with the combination achieved bone regeneration within 4 wk in mouse calvarial bone defects. Thus, we successfully identified the potent combination of genes for bone regeneration, which helped broaden cell sources.—Ohba, S., Ikeda, T., Kugimiya, F., Yano, F., Lichtler, A. C., Nakamura, K., Takato, T., Kawaguchi, H., Chung, U. I. Identification of a potent combination of osteogenic genes for bone regeneration using embryonic stem (ES) cell-based sensor.


Key Words: osteogenesis • screening • biosensor • cell sheet







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