Medium acidosis drives cardiac differentiation during mesendoderm cell fate specification from human pluripotent stem cells

Stem Cell Reports. 2024 Sep 10;19(9):1304-1319. doi: 10.1016/j.stemcr.2024.07.012. Epub 2024 Aug 22.

Abstract

Effective lineage-specific differentiation is essential to fulfilling the great potentials of human pluripotent stem cells (hPSCs). In this report, we investigate how modulation of medium pH and associated metabolic changes influence mesendoderm differentiation from hPSCs. We show that daily medium pH fluctuations are critical for the heterogeneity of cell fates in the absence of exogenous inducers. Acidic environment alone leads to cardiomyocyte generation without other signaling modulators. In contrast, medium alkalinization is inhibitory to cardiac fate even in the presence of classic cardiac inducers. We then demonstrate that acidic environment suppresses glycolysis to facilitate cardiac differentiation, while alkaline condition promotes glycolysis and diverts the differentiation toward other cell types. We further show that glycolysis inhibition or AMPK activation can rescue cardiac differentiation under alkalinization, and glycolysis inhibition alone can drive cardiac cell fate. This study highlights that pH changes remodel metabolic patterns and modulate signaling pathways to control cell fate.

MeSH terms

  • AMP-Activated Protein Kinases / metabolism
  • Acidosis / metabolism
  • Cell Differentiation* / drug effects
  • Cell Line
  • Cell Lineage / drug effects
  • Culture Media / chemistry
  • Culture Media / pharmacology
  • Endoderm / cytology
  • Endoderm / metabolism
  • Glycolysis*
  • Humans
  • Hydrogen-Ion Concentration
  • Mesoderm / cytology
  • Mesoderm / metabolism
  • Myocytes, Cardiac* / cytology
  • Myocytes, Cardiac* / drug effects
  • Myocytes, Cardiac* / metabolism
  • Pluripotent Stem Cells* / cytology
  • Pluripotent Stem Cells* / drug effects
  • Pluripotent Stem Cells* / metabolism
  • Signal Transduction / drug effects

Substances

  • Culture Media
  • AMP-Activated Protein Kinases