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M705621200v1
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Papers In Press, published online ahead of print November 16, 2007
J. Biol. Chem, 10.1074/jbc.M705621200
Submitted on July 9, 2007
Revised on October 10, 2007
Accepted on November 16, 2007

Heparan sulfate regulates self-renewal and pluripotency of embryonic stem cells

Norihiko Sasaki, Kazuhiko Okishio, Kumiko Ui-Tei, Kaoru Saigo, Akiko Kinoshita-Toyoda, Hidenao Toyoda, Tomoaki Nishimura, Yasuo Suda, Michiko Hayasaka, Kazunari Hanaoka, Seiji Hitoshi, Kazuyuki Ikenaka, and Shoko Nishihara

Laboratory of Cell Biology, Department of Bioinformatics, Faculty of Engineering, Soka University, Tokyo 192-8577

Corresponding Author: shoko{at}t.soka.ac.jp

Embryonic stem (ES) cell self-renewal and pluripotency are maintained by several signaling cascades and by expression of intrinsic factors, such as Oct3/4 and Nanog. The signaling cascades are activated by extrinsic factors, such as leukemia inhibitory factor, bone morphogenic protein and Wnt. However, the mechanism that regulates extrinsic signaling in ES cells is unknown. Heparan sulfate (HS) chains are ubiquitously present as the cell surface proteoglycans and are known to play crucial roles in regulating several signaling pathways. Here, we investigated whether HS chains on ES cells are involved in regulating signaling pathways that are important for the maintenance of ES cells. RNA interference-mediated knockdown of HS chain elongation inhibited mouse ES cell self-renewal and induced spontaneous differentiation of the cells into extraembryonic endoderm. Furthermore, autocrine/paracrine Wnt/beta -catenin signaling through HS chains was found to be required for the regulation of Nanog expression. We propose that HS chains are important for the extrinsic signaling required for mouse ES cell self-renewal and pluripotency.


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Proc. Natl. Acad. Sci. USAHome page
M. K. Furue, J. Na, J. P. Jackson, T. Okamoto, M. Jones, D. Baker, R.-I. Hata, H. D. Moore, J. D. Sato, and P. W. Andrews
Heparin promotes the growth of human embryonic stem cells in a defined serum-free medium
PNAS, September 9, 2008; 105(36): 13409 - 13414.
[Abstract] [Full Text] [PDF]




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