Glucose oxidation drives trunk neural crest cell development and fate

J Cell Sci. 2023 Aug 15;136(16):jcs260607. doi: 10.1242/jcs.260607. Epub 2023 Aug 15.

Abstract

Bioenergetic metabolism is a key regulator of cellular function and signaling, but how it can instruct the behavior of cells and their fate during embryonic development remains largely unknown. Here, we investigated the role of glucose metabolism in the development of avian trunk neural crest cells (NCCs), a migratory stem cell population of the vertebrate embryo. We uncovered that trunk NCCs display glucose oxidation as a prominent metabolic phenotype, in contrast to what is seen for cranial NCCs, which instead rely on aerobic glycolysis. In addition, only one pathway downstream of glucose uptake is not sufficient for trunk NCC development. Indeed, glycolysis, mitochondrial respiration and the pentose phosphate pathway are all mobilized and integrated for the coordinated execution of diverse cellular programs, epithelial-to-mesenchymal transition, adhesion, locomotion, proliferation and differentiation, through regulation of specific gene expression. In the absence of glucose, the OXPHOS pathway fueled by pyruvate failed to promote trunk NCC adaptation to environmental stiffness, stemness maintenance and fate-decision making. These findings highlight the need for trunk NCCs to make the most of the glucose pathway potential to meet the high metabolic demands appropriate for their development.

Keywords: Bioenergetics; Cell migration; Fate decision; Glycolysis; Neural crest; Oxidative phosphorylation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Adhesion
  • Cells, Cultured
  • Glucose* / metabolism
  • In Vitro Techniques
  • Metabolic Networks and Pathways
  • Neural Crest* / growth & development
  • Neural Crest* / metabolism
  • Neural Tube / cytology
  • Oxidative Phosphorylation
  • Quail* / growth & development
  • Quail* / metabolism

Substances

  • Glucose