Eliminating the confounding effects of human pluripotent #stemcell co-culture with MEFs:
@grazianomartello.bsky.social @leeboratory.bsky.social @jzylicz.bsky.social and collaborators describe a serum coating approach for feeder-free culture of naïve hPSCs
link.springer.com/article/10.1...
Posts by Jan Żylicz
I thought it’s just a junior PI phenomenon where everything is happening in slow motion. But now think everyone is affected. Not enough editors and inflated numbers of experiments.
I'm looking forward to this event!
Do you want to play a key role in running a cutting-edge stem cell and embryology lab at reNEW @ucph.bsky.social ? We’re hiring a Lab Manager to support our team and help with stem cell and animal work. Apply before Feb. 1st : rb.gy/d5uf17
🧵1/14 Preprint thread! Can we predict a cell’s fate based on its dynamics? 🔮 Our new study unveils a framework for watching development unfold in real-time, revealing how a cell's shape and movement encode info about its future fate. 🔬📄 Preprint: tinyurl.com/4shf8v4x
🙏 A. Wenzel, K. Uściło, S. Kompocholi, S. Bages-Arnal,
@gemnov.bsky.social
Using HDAC3 knockout embryos, we show that they typically fail to implant, and if they manage, they are very small and upregulate the most active genes. It is fascinating how a repressor of enhancers regulates the most active genes, allowing for development and to proceed.
At enhancers HDAC3 fights with P300, an activator, to reduce the expression of the most active fraction of the genome. Losing HDAC3 boosts the levels of pluripotency and prevents them from efficiently differentiating.
We found that HDAC3, a histone deacetylase, is an intriguing transcriptional repressor. Rather than maintaining genes in a silent state, it is recruited to the most active enhancers of mouse pluripotent stem cells.
Genes are not On/Off switches. In a new preprint we show that HDAC3 is key to establish correct transcriptional dose in development. Gr8 work from N. Stamidis @ucph.bsky.social and collab. @jamiehackett.bsky.social @gregersenlab.bsky.social . Huge thx to all authors! www.biorxiv.org/content/10.1...
It’s always a bit awkward to write about personal experiences. I tried to touch on what Pride means to me and ended up reflecting on heteronormativity, passing, and allyship. Thank you @slefkopoulos.bsky.social for the great opportunity! @ucph.bsky.social
#LGBTQIA+ #PRIDE #Diversity
There is still some time to secure your spot at the next Niche meeting in CPH. We have a great lineup of speakers! @novo-nordisk.bsky.social sciencecluster.dk/event/confer...
I could not have been more proud! The first student from the lab just defended his PhD in great style!! Congratulations Arnau Casòliba Melich !!! A huge thank you to the committee @bernasozen.bsky.social Ana Boskovic and @aramariaceleste.bsky.social
Wow huge congratulations!
It was fun to chat with @amjeve.bsky.social about my fantastic mentors and how it is to become independent at reNEW_Global @ucph.bsky.social
💫NEW: @jzylicz.bsky.social & co show that dimethyl α-ketoglutarate enhances the production and functional maturation of human #trophectoderm - like cells from embryonic #StemCells by regulating histone acetyltransferase activity and the pluripotency network.
bit.ly/3EGflmL
We also find that there is robust reductive glutamine metabolism in stem cells with glutamine becoming the most prominent source of carbon for histone acetylation
Pyruvate emerged as a vital metabolic nexus in pluripotent stem cells, with high pyruvate carboxylase and malic enzyme activity. Functionally, this is crucial for the timely exit from naive pluripotency and maintaining histone acetylation levels.
We used 13C labeling and imaging MS to uncover how metabolism rewires when the mouse embryo implants. We found that there is no simple TCA cycle shutdown; rather, there is intricate rewiring. This process is recapitulated in pluripotent stem cells cultured under low oxygen.
In a new preprint with @trabelink.bsky.social, T. Moritz & @bonalditiziana.bsky.social, we find that implantation leads to rewiring of the TCA cycle to support histone acetylation turnover and exit from naïve pluripotency. Gr8 work of @elenikafkia.bsky.social D. Pladevall-Morera et al. rb.gy/clk8vm
This was a great collaboration lead by Karlien Van Nerum with @sophiepetropoulos.bsky.social ThomasMoritz and EpiQMax.
Can metabolism regulate more than bioenergetics during human development? Our new study says YES! We show that metabolism influences cell fate choice in human naïve pluripotent stem cells, histone acetylation, and trophectoderm maturation. rb.gy/spqr9j
@natcellbio.nature.com
Become Our New Faculty Colleague! We are looking for a junior Principal Investigator to expand their stem cell research towards translational outcomes.
reNEW Copenhagen @ucph.bsky.social
#stemcell #diversity #faculty #regenerativemedicine shorturl.at/m9Zko
It was very fun to contribute to this article: "But genes are not the whole story. New research has shown the extent to which cell metabolism (...) has an important, underappreciated role in directing cell fates". www.quantamagazine.org/how-metaboli... QuantaMagazine @ucph.bsky.social
Only 2 weeks left to apply! 16 fantastic positions available, also @ucph.bsky.social . For our project remember to apply both at shorturl.at/yf7Qq & nuclear-dn.eu.
We're hiring a motivated PhD student! Join reNEW @ucph.bsky.social & @nucleardn.bsky.social to study how metabolism regulates chromatin & stem cell fate thanks to generous Marie Skłodowska-Curie Fellowship. Remember to apply both at shorturl.at/yf7Qq & nuclear-dn.eu.
The grass is always greener on the other side. But for now Denmark is a pretty nice place to live and do research! We mainly complain about the weather.
I’m very excited about this collaborative project! We managed to significantly scale up and streamline human blastoid generation without the use of feeders. @leeboratory.bsky.social @grazianomartello.bsky.social @pasquelab.bsky.social and Nicolas Rivron @ucph.bsky.social
Congratulations!!! This is great news!!