Energy metabolism in nuclear reprogramming

Research output: Contribution to journalArticle

41 Citations (Scopus)

Abstract

Nuclear reprogramming with stemness factors enables resetting of somatic differentiated tissue back to the pluripotent ground state. Recent evidence implicates mitochondrial restructuring and bioenergetic plasticity as key components underlying execution of orchestrated dedifferentiation and derivation of induced pluripotent stem cells. Aerobic to anaerobic transition of somatic oxidative energy metabolism into a glycolytic metabotype promotes proficient reprogramming, establishing a novel regulator of acquired stemness. Metabolomic profiling has further identified specific metabolic remodeling traits defining lineage redifferentiation of pluripotent cells. Therefore, mitochondrial biogenesis and energy metabolism comprise a vital axis for biomarker discovery, intimately reflecting the molecular dynamics fundamental for the resetting and redirection of cell fate.

Original languageEnglish (US)
Pages (from-to)715-729
Number of pages15
JournalBiomarkers in Medicine
Volume5
Issue number6
DOIs
StatePublished - Dec 2011

Fingerprint

Energy Metabolism
Induced Pluripotent Stem Cells
Metabolomics
Biomarkers
Organelle Biogenesis
Molecular Dynamics Simulation
Stem cells
Ground state
Plasticity
Molecular dynamics
Tissue
Cellular Reprogramming

Keywords

  • biomarker
  • differentiation
  • glycolysis
  • induced pluripotent stem cell
  • metabolomics
  • metabotype
  • mitochondria
  • oxidative metabolism
  • regenerative medicine
  • stem cells

ASJC Scopus subject areas

  • Clinical Biochemistry
  • Biochemistry, medical
  • Drug Discovery

Cite this

Energy metabolism in nuclear reprogramming. / Folmes, Clifford; Nelson, Timothy J; Terzic, Andre.

In: Biomarkers in Medicine, Vol. 5, No. 6, 12.2011, p. 715-729.

Research output: Contribution to journalArticle

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