DNA methylation is indispensable for leukemia inhibitory factor dependent embryonic stem cells reprogramming
B. Wu, Y. Li, B. Li, B. Zhang, Y. Wang, L. Li, G. Peng, Y. Fu, S. Li, C. Chen, A. Surani, F. Tang, X. Li, S. Bao
Abstract
Naive pluripotency can be maintained by the 2i/LIF supplements (CHIR99021, PD0325901 and LIF), which primarily affect canonical WNT, FGF/ERK, and JAK/STAT3 signaling. However, whether one of these tripartite supplements alone is sufficient to maintain naive self-renewal remain unclear. Here we show that LIF alone is sufficient to induce reprogramming of 2i/LIF cultured ESCs (2i/L-ESCs) to ESCs with hypermethylated state (L-ESCs). In vitro, upon withdrawal of 2i, 2i/L-ESCs overcome the epigenetic barrier and DNA hypermethylated, which accompanies transcriptional changes and subsequent establishment of epigenetic memory. Global transcriptome features also show that L-ESCs are close to 2i/L-ESCs and in a stable state between naive and primed pluripotency. Notably, our results demonstrate that DNA methylation was indispensable for LIF-dependent mouse ESCs reprogramming and self-renew. LIF-dependent ESCs reprogramming efficiency is significantly increased in serum treatment and reduced in Dnmt3a or Dnmt3l knockout ESCs. Importantly, unlike epiblast and EpiSCs, L-ESCs contribute to somatic tissues and germ cells in chimaeras. Such simple culture system of ESCs is more conducive to clarify the molecular mechanism of ESCs in vitro culture. SignificanceEmbryonic stem cell (ESCs) exhibit naive pluripotency which reflects their ability to contribute to all embryonic lineages upon injection into blastocyst. ESCs were originally derived by co-culture with feeder cells and fetal calf serum. In this manuscript, we took a detailed approach to dissect the roles of LIF alone in ESC reprogramming of 2i/LIF cultured ESCs (2i/L-ESCs). Here, for the first time, we derived stable hypermethylated pluripotent ESCs under culture of LIF alone (L-ESCs). We further assessed L-ESCs properties both in vitro and in vivo, and provide molecular insights to the mechanism which allows LIF alone to maintain pluripotency and a hypermethylated state. We believe these findings are novel and valuable for future ESCs study.
02 /Specification & Classification
Click any tag to browse matching papersReproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Mouse Embryonic Stem Cell Pluripotency Factors Regulate RNA Methylation
Laura J. Sedivy, Gabrielle Brandt, … Christopher J. Phiel·bioRxiv·Feb 23, 2023
- The catalytic-independent function of LSD1 modulates the epigenetic landscape of mouse embryonic stem cells
Sandhya Malla, Kanchan Kumari, … Francesca Aguiló·bioRxiv·Jun 29, 2023
- Lipids Maintain Genomic Stability and Developmental Potency of Murine Pluripotent Stem Cells
Liangwen Zhong, Miriam Gordillo, … Duancheng Wen·bioRxiv·Aug 12, 2022
- The distinct effects of MEK and GSK3 inhibition upon the methylome and transcriptome of mouse embryonic stem cells
Julia Spindel, Christel Krueger, … Wolf Reik·bioRxiv·Nov 18, 2021
- A lncRNA/Lin28/Let7 Axis Coupled To DNA Methylation Fine Tunes The Dynamics Of A Cell State Transition
M. A. Li, P. P. Amaral, … A. Smith·bioRxiv·Apr 26, 2017
- A Universal 6iL/E4 Culture System for Deriving and Maintaining Embryonic Stem Cells Across Mammalian Species
Duo Wang, Hao Ming, … Qi‐Long Ying·Cell ResearchPeer-reviewed·Jul 13, 2026