TY - JOUR
T1 - NAC regulates metabolism and cell fate in intestinal stem cells
AU - Ramalho, Sofia
AU - Alkan, Ferhat
AU - Prekovic, Stefan
AU - Jastrzebski, Katarzyna
AU - Barberà, Eric Pintó
AU - Hoekman, Liesbeth
AU - Altelaar, Maarten
AU - de Heus, Cecilia
AU - Liv, Nalan
AU - Rodríguez-Colman, Maria J.
AU - Yilmaz, Mehmet
AU - van der Kammen, Rob
AU - Fedry, Juliette
AU - de Gooijer, Mark C.
AU - Suijkerbuijk, Saskia Jacoba Elisabeth
AU - Faller, William J.
AU - Silva, Joana
N1 - Publisher Copyright:
Copyright © 2025 The Authors.
PY - 2025/1/10
Y1 - 2025/1/10
N2 - Intestinal stem cells (ISCs) face the challenge of integrating metabolic demands with unique regenerative functions. Studies have shown an intricate interplay between metabolism and stem cell capacity; however, it is still not understood how this process is regulated. Combining ribosome profiling and CRISPR screening in intestinal organoids, we identify the nascent polypeptide-associated complex (NAC) as a key mediator of this process. Our findings suggest that NAC is responsible for relocalizing ribosomes to the mitochondria and regulating ISC metabolism. Upon NAC inhibition, intestinal cells show decreased import of mitochondrial proteins, which are needed for oxidative phosphorylation, and, consequently, enable the cell to maintain a stem cell identity. Furthermore, we show that overexpression of NACα is sufficient to drive mitochondrial respiration and promote ISC identity. Ultimately, our results reveal the pivotal role of NAC in regulating ribosome localization, mitochondrial metabolism, and ISC function, providing insights into the potential mechanism behind it.
AB - Intestinal stem cells (ISCs) face the challenge of integrating metabolic demands with unique regenerative functions. Studies have shown an intricate interplay between metabolism and stem cell capacity; however, it is still not understood how this process is regulated. Combining ribosome profiling and CRISPR screening in intestinal organoids, we identify the nascent polypeptide-associated complex (NAC) as a key mediator of this process. Our findings suggest that NAC is responsible for relocalizing ribosomes to the mitochondria and regulating ISC metabolism. Upon NAC inhibition, intestinal cells show decreased import of mitochondrial proteins, which are needed for oxidative phosphorylation, and, consequently, enable the cell to maintain a stem cell identity. Furthermore, we show that overexpression of NACα is sufficient to drive mitochondrial respiration and promote ISC identity. Ultimately, our results reveal the pivotal role of NAC in regulating ribosome localization, mitochondrial metabolism, and ISC function, providing insights into the potential mechanism behind it.
UR - http://www.scopus.com/inward/record.url?scp=85215122544&partnerID=8YFLogxK
U2 - 10.1126/sciadv.adn9750
DO - 10.1126/sciadv.adn9750
M3 - Article
C2 - 39772672
AN - SCOPUS:85215122544
VL - 11
SP - eadn9750
JO - Science advances
JF - Science advances
IS - 2
M1 - eadn9750
ER -