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Wnt/β-catenin and LIF/Stat3 signaling pathways converge on Sp5 to promote mouse embryonic stem cell self-renewal
Author(s) -
Shoudong Ye,
Dongming Zhang,
Fei Cheng,
Daniel N. Wilson,
Jeffrey Mackay,
Kan He,
Qian Ban,
Feng Lv,
Saifei Huang,
Dahai Liu,
QiLong Ying
Publication year - 2015
Publication title -
journal of cell science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.384
H-Index - 278
eISSN - 1477-9137
pISSN - 0021-9533
DOI - 10.1242/jcs.177675
Subject(s) - wnt signaling pathway , biology , epiblast , embryonic stem cell , microbiology and biotechnology , leukemia inhibitory factor , stem cell , signal transduction , catenin , stat3 , embryogenesis , genetics , gastrulation , embryo , gene
Activation of leukemia inhibitor factor (LIF)-Stat3 or Wnt/β-catenin signaling promotes mouse embryonic stem cell (mESC) self-renewal. A myriad of downstream targets have been identified in the individual signal pathways, but their common targets remain largely elusive. In this study, we found that the LIF-Stat3 and Wnt/β-catenin signaling pathways converge on Sp5 to promote mESC self-renewal. Forced Sp5 expression can reproduce partial effects of Wnt/β-catenin signaling but mimics most features of LIF-Stat3 signaling to maintain undifferentiated mESCs. Moreover, Sp5 is able to convert mouse epiblast stem cells into a naïve pluripotent state. Thus, Sp5 is an important component of the regulatory network governing mESC naïve pluripotency.

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