Glycolytic activity instructs germ layer proportions through regulation of Nodal and Wnt signaling
Year: 2025
Type: article
Abstract: During embryonic development, cells exit pluripotency to give rise to the three germ layers. Metabolic pathways influence cell fate decisions by modulating the epigenetic, transcriptional, and signalling states of cells. However, the interplay between metabolism and the major signalling pathways that drive the emergence of ectoderm, mesoderm, and endoderm remains poorly understood. Here, we demonstrate an instructive role of glycolytic activity in activating signalling pathways involved in mesoderm and endoderm induction. Using an in vitro model system for mouse gastrulation, we observed that inhibiting glycolysis prevents the upregulation of primitive streak markers, resulting in a significant increase in ectodermal cell fates at the expense of mesodermal and endodermal lineages. We demonstrate that this relationship is dose-dependent, enabling metabolic control of germ layer proportions through exogenous glucose levels. Mechanistically, we found that glycolysis inhibition leads to the downregulation of Wnt, Nodal, and Fgf signalling. Notably, this metabolic phenotype was rescued by Nodal or Wnt signalling agonists in the absence of glycolytic activity, suggesting that glycolytic activity acts upstream of both signalling pathways. Our work underscores the dependence of specific signalling pathways on metabolic conditions and provides mechanistic insight into the nutritional regulation of cell fate decision making.
Source: Cell stem cell
Institutions: European Molecular Biology Laboratory, University of Michigan, Michigan Medicine, University of Cambridge, MRC Toxicology Unit, Medical Research Council, European Molecular Biology Laboratory, Max Planck Institute of Molecular Cell Biology and Genetics, Physics of Life, Technische Universität Dresden
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: hybrid
Estimated APC paid: $10,400
Funders: National Science Foundation, Gordon and Betty Moore Foundation, Human Frontier Science Program, European Molecular Biology Laboratory, European Commission, Human Frontier Science Program, Horizon 2020 Framework Programme, National Institute of General Medical Sciences, Kavli Institute for Theoretical Physics, University of California, Santa Barbara, H2020 European Research Council, H2020 Marie Skłodowska-Curie Actions, HORIZON EUROPE European Research Council
Awards: EMBL Interdisciplinary Postdoc Programme 4, G1709206515, G2798721979, G3719371286, RECODE: Harnessing Stem Cell Heterogeneity to Navigate Lineage Specification and Maturity in Real Time, G434337789, G4462369699, G4937468798, G5072843579, G537432605, G5970826584, G597488960, G6357308207, G6812749935, EMBL Interdisciplinary Postdoc Programme 4, Kavli Institute for Theoretical Physics, G876022237, Multifunctional morphogens: patterning precision and mesoderm migration
OpenAlex ID: W4409502808
