TY - JOUR
T1 - Self-renewal of a purified Tie2+ hematopoietic stem cell population relies on mitochondrial clearance
AU - Ito, Kyoko
AU - Turcotte, Raphaël
AU - Cui, Jinhua
AU - Zimmerman, Samuel E.
AU - Pinho, Sandra
AU - Mizoguchi, Toshihide
AU - Arai, Fumio
AU - Runnels, Judith M.
AU - Alt, Clemens
AU - Teruya-Feldstein, Julie
AU - Mar, Jessica C.
AU - Singh, Rajat
AU - Suda, Toshio
AU - Lin, Charles P.
AU - Frenette, Paul S.
AU - Ito, Keisuke
N1 - Publisher Copyright:
© 2016, American Association for the Advancement of Science. All rights reserved.
PY - 2016/12/2
Y1 - 2016/12/2
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=84991108288&partnerID=8YFLogxK
U2 - 10.1126/science.aaf5530
DO - 10.1126/science.aaf5530
M3 - Article
C2 - 27738012
AN - SCOPUS:84991108288
SN - 0036-8075
VL - 354
SP - 1156
EP - 1160
JO - Science
JF - Science
IS - 6316
ER -