Calorie restriction activates a gastric Notch-FOXO1 pathway to expand ghrelin cells

J Cell Biol. 2024 Oct 7;223(10):e202305093. doi: 10.1083/jcb.202305093. Epub 2024 Jul 3.

Abstract

Calorie restriction increases lifespan. Among the tissue-specific protective effects of calorie restriction, the impact on the gastrointestinal tract remains unclear. We report increased numbers of chromogranin A-positive (+), including orexigenic ghrelin+ cells, in the stomach of calorie-restricted mice. This effect was accompanied by increased Notch target Hes1 and Notch ligand Jag1 and was reversed by blocking Notch with DAPT, a gamma-secretase inhibitor. Primary cultures and genetically modified reporter mice show that increased endocrine cell abundance is due to altered Lgr5+ stem and Neurog3+ endocrine progenitor cell proliferation. Different from the intestine, calorie restriction decreased gastric Lgr5+ stem cells, while increasing a FOXO1/Neurog3+ subpopulation of endocrine progenitors in a Notch-dependent manner. Further, activation of FOXO1 was sufficient to promote endocrine cell differentiation independent of Notch. The Notch inhibitor PF-03084014 or ghrelin receptor antagonist GHRP-6 reversed the phenotypic effects of calorie restriction in mice. Tirzepatide additionally expanded ghrelin+ cells in mice. In summary, calorie restriction promotes Notch-dependent, FOXO1-regulated gastric endocrine cell differentiation.

MeSH terms

  • Animals
  • Basic Helix-Loop-Helix Transcription Factors / genetics
  • Basic Helix-Loop-Helix Transcription Factors / metabolism
  • Caloric Restriction*
  • Cell Differentiation
  • Cell Proliferation
  • Forkhead Box Protein O1* / genetics
  • Forkhead Box Protein O1* / metabolism
  • Gastric Mucosa / metabolism
  • Ghrelin* / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism
  • Receptors, G-Protein-Coupled / genetics
  • Receptors, G-Protein-Coupled / metabolism
  • Receptors, Notch* / genetics
  • Receptors, Notch* / metabolism
  • Signal Transduction*
  • Stem Cells / metabolism
  • Stomach
  • Transcription Factor HES-1 / genetics
  • Transcription Factor HES-1 / metabolism

Substances

  • Ghrelin
  • Forkhead Box Protein O1
  • Receptors, Notch
  • Foxo1 protein, mouse
  • Receptors, G-Protein-Coupled
  • Basic Helix-Loop-Helix Transcription Factors
  • Lgr5 protein, mouse
  • Nerve Tissue Proteins
  • Neurog3 protein, mouse
  • Transcription Factor HES-1
  • Hes1 protein, mouse