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Sox9 and programming of liver and pancreatic progenitors
Yoshiya Kawaguchi
Yoshiya Kawaguchi
Published May 1, 2013
Citation Information: J Clin Invest. 2013;123(5):1881-1886. https://doi.org/10.1172/JCI66022.
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Review Series

Sox9 and programming of liver and pancreatic progenitors

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Abstract

Recent advances in developmental biology have greatly expanded our understanding of progenitor cell programming and the fundamental roles that Sox9 plays in liver and pancreas organogenesis. In the last 2 years, several studies have dissected the behavior of the Sox9+ duct cells in adult organs, but conflicting results have left unanswered the long-standing question of whether physiologically functioning progenitors exist in adult liver and pancreas. On the other hand, increasing evidence suggests that duct cells function as progenitors in the tissue restoration process after injury, during which embryonic programs are sometimes reactivated. This article discusses the role of Sox9 in programming liver and pancreatic progenitors as well as controversies in the field.

Authors

Yoshiya Kawaguchi

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Figure 1

Tamoxifen-inducible Cre-mediated lineage tracing.

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Tamoxifen-inducible Cre-mediated lineage tracing.
Cre recombinase is fus...
Cre recombinase is fused with the ligand-binding domain of the estrogen receptor. Tamoxifen administration enables the CreER fusion protein to enter the nucleus then excise the STOP cassette of ROSA26r, resulting in permanent labeling of the progeny. Such strategies have been instrumental to understanding the role of Sox9 in pancreatic and liver progenitor cells.

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