| Literature DB >> 18024963 |
Norihiko Sasaki1, Kazuhiko Okishio2, Kumiko Ui-Tei3, Kaoru Saigo3, Akiko Kinoshita-Toyoda4, Hidenao Toyoda4, Tomoaki Nishimura5, Yasuo Suda6, Michiko Hayasaka7, Kazunari Hanaoka7, Seiji Hitoshi8, Kazuhiro Ikenaka8, Shoko Nishihara9.
Abstract
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.Entities:
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Year: 2007 PMID: 18024963 DOI: 10.1074/jbc.M705621200
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157