WNT/β-catenin pathway up-regulates Stat3 and converges on LIF to prevent differentiation of mouse embryonic stem cells
Autor: | Teng-Guo Li, Dong-Feng Zhao, Jing Hao, Guang-Quan Zhao, Xiaoxia Qi |
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Rok vydání: | 2006 |
Předmět: |
Pluripotency
Male Pluripotent Stem Cells STAT3 Transcription Factor Embryonic stem cells Mouse Cellular differentiation Biology Leukemia Inhibitory Factor Wnt-5a Protein STAT3 WNT6 Mice Proto-Oncogene Proteins Animals Molecular Biology Cells Cultured beta Catenin Interleukin-6 Wnt signaling pathway LRP6 Cell Differentiation LRP5 WNT/β-catenin Cell Biology Embryo Mammalian Embryonic stem cell Coculture Techniques Up-Regulation Cell biology Wnt Proteins Female Stem cell Growth factors Leukemia inhibitory factor Signal Transduction Developmental Biology |
Zdroj: | Developmental Biology. 290:81-91 |
ISSN: | 0012-1606 |
DOI: | 10.1016/j.ydbio.2005.11.011 |
Popis: | Embryonic stem (ES) cells rely on growth factors provided by feeder cells or exogenously to maintain their pluripotency. In order to identify such factors, we have established sub-lines of STO feeder cells which exhibit variable ability in supporting ES cell self-renewal. Functional screening identifies WNT5A and WNT6 as STO cell-produced factors that potently inhibit ES cell differentiation in a serum-dependent manner. Furthermore, direct activation of beta-catenin without disturbing the upstream components of the WNT/beta-catenin pathway fully recapitulates the effect of WNTs on ES cells. Importantly, the WNT/beta-catenin pathway up-regulates the mRNA for Stat3, a known regulator of ES cell self-renewal in the mouse. Finally, LIF is able to mimic the serum effect to act synergistically with WNT proteins to inhibit ES cell differentiation. Therefore, our study reveals part of the molecular mechanisms by which the WNT/beta-catenin pathway acts to prevent ES cell differentiation through convergence on the LIF/JAK-STAT pathway at the level of STAT3. |
Databáze: | OpenAIRE |
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