Self-renewal of a purified Tie2+ hematopoietic stem cell population relies on mitochondrial clearance

Science. 2016 Dec 2;354(6316):1156-1160. doi: 10.1126/science.aaf5530. Epub 2016 Oct 13.

Abstract

A single hematopoietic stem cell (HSC) is capable of reconstituting hematopoiesis and maintaining homeostasis by balancing self-renewal and cell differentiation. The mechanisms of HSC division balance, however, are not yet defined. Here we demonstrate, by characterizing at the single-cell level a purified and minimally heterogeneous murine Tie2+ HSC population, that these top hierarchical HSCs preferentially undergo symmetric divisions. The induction of mitophagy, a quality control process in mitochondria, plays an essential role in self-renewing expansion of Tie2+ HSCs. Activation of the PPAR (peroxisome proliferator-activated receptor)-fatty acid oxidation pathway promotes expansion of Tie2+ HSCs through enhanced Parkin recruitment in mitochondria. These metabolic pathways are conserved in human TIE2+ HSCs. Our data thus identify mitophagy as a key mechanism of HSC expansion and suggest potential methods of cell-fate manipulation through metabolic pathways.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Self Renewal*
  • Cell Separation
  • Fatty Acids / metabolism
  • Green Fluorescent Proteins / analysis
  • Green Fluorescent Proteins / metabolism
  • Hematopoiesis / physiology*
  • Hematopoietic Stem Cells / chemistry
  • Hematopoietic Stem Cells / physiology*
  • Metabolic Networks and Pathways
  • Mice
  • Mice, Inbred C57BL
  • Mitochondria / physiology*
  • Mitophagy / genetics
  • Mitophagy / physiology*
  • Oxidation-Reduction
  • Peroxisome Proliferator-Activated Receptors / metabolism
  • Receptor, TIE-2 / analysis
  • Single-Cell Analysis
  • Ubiquitin-Protein Ligases / genetics
  • Ubiquitin-Protein Ligases / metabolism

Substances

  • Fatty Acids
  • Peroxisome Proliferator-Activated Receptors
  • Green Fluorescent Proteins
  • Ubiquitin-Protein Ligases
  • parkin protein
  • Receptor, TIE-2
  • Tek protein, mouse